Tag Archives: NCIM

How you can turn a disposable surgical mask into a virus killer

https://ncimexico.files.wordpress.com/2020/03/how-to-make-your-own-antiviral-mask-ncim-march-2019-1.pdf

Correction: On page 3 of the how to guide this entry “A suitable 1 or 2 ounce (30 or 60 mL) spray bottle (Glass is probably best as plastics contain chemicals that could leach into the salt-surfactant solution) Look for no clog pumps.” should have read “A suitable 6 oz (177 mL) spray bottle……etc.”

NCIM has won many battles against advanced & end-stage cancer

https://ncimexico.files.wordpress.com/2018/05/hope-for-the-hopeless.pdf

 

 

Four important points about Nova Cells Institute

cropped-nova-cells-bannerNova Cells Institute has never worked with embryonic or fetal stem cells, and never will. Embryonic and fetal stem cells can produce tumors (These are classified as pluripotent” which means they can form teratomas and other tumors in certain instances such as being injected into the central nervous system). The adult stem cells Nova Cells uses (umbilical cord, Wharton’s Jelly, placenta-derived, and a patient’s own bone marrow) are “multipotent” which limits the body cell types they can become (These stem cells do not form teratomas or such. Some private stem cell clinics in Europe and the US have injected adult stem cells into organs such as kidneys and eyes which caused problems and complications. Nova Cells Institute has never injected stem cells into an organ).
Let’s be very clear about these points and a few others:

(1) Nova Cells was established in 2009. There are other companies that came along later on which use “Nova” in their company title, but these are NOT affiliated in any way with Nova Cells Institute of Mexico (NCIM).

(2) Nova Cells Institute has never used embryonic or fetal stem cells and never will (They can form tumors under certain circumstances).

(3) Nova Cells Institute only uses multipotent adult stem cells derived from umbilical cord blood, Wharton’s Jelly, placental tissue, and a patient’s own bone marrow.

(4) Nova Cells Institute administers stem cells by intravenous drip (On rare occasions Nova Cells affiliated doctors recommend an intrathecal or spinal tap infusion of cells. Everything related to this is spelled out, a process called “informed consent”. Patients who prefer not to do this are given cells by intravenous or IV drip).

Improvements coming out of the gate for Evie Morgan (3 year old little girl with Spina bifida)

Three year old Evie Morgan has spina bifida and a Facebook page devoted to her journey to betterment at https://www.facebook.com/evieswarriors/. She was treated in Mexico by Nova Cells Institute doctors during April (2016) and soon her Mum, Heather, was emailing NCIM patient care coordinator, Grace Odgers PhD cand., a series of positive reports and video clips.  Heather also made posts to the aforementioned Facebook page — three of which follow further down below.

Evie Morgan - April 2016
Evie in Mexico getting IV infusion

 

On 4-27-16 Heather Morgan sent this email message to NCIM’s Grace Odgers, PhD cand.:

We felt very comfortable in the hospital. The room was very clean and had a private bathroom and sink. The pediatrician, Dr. Sanchez, was amazing and Evie loved her so much. Dr. Sanchez spoke great English and we had no trouble understanding her at all. The nurses were very attentive to whatever it was that Evie needed and Grace was always right there to translate for us if they had questions or we wanted to say something. The procedure was quick and painless. Within 5 minutes of receiving the treatment Evie began moving her toes. In the week and a half since treatment Evie is still able to move her toes on command (prior to treatment Evie only had very little involuntary movement of her toes), she is urinating more on her own and has very increased balance. She is now beginning to walk much longer distances with her canes (before she had a walker). At her next urology appointment we are going to be able to start discussing next steps in seeing how her bladder can fully function without medication. We are very pleased with the results we have seen thus far and can’t wait to see what else Evie is going to do!

 Evie’s Warriors – Posted on April 22, 2016 (Friday)
 

This video was taken 2 days after stem cells. Evie is now able to move her toes on command! Before it was completely involuntary movement. Pardon her sassiness at the beginning 😂 Evie also has incredibly improved balance and is able to walk much longer distances with her canes! ‪#‎evieswarriors‬

EVIE MORGAN - 2 days after SCT treatment - April 2016
Go to Evie’s Warriors Facebook page to watch

 

Evie’s Warriors

April 16 at 5:46pm ·

Evie is showing improvements in her bladder function and abilities since yesterday. We aren’t sure if this is going to be a consistent thing but we are definitely watching now. This is nuts.

Sorry for lack of updates. Everything went perfectly and the treatment is now complete. Within minutes Evie was flexing her right ankle when asked and wiggling all 5 toes. Some of the movement is involuntary right now as the cells are being repaired. We will continue to see results for a few months. Thank you all for supporting our girl! ‪#‎evieswarriors‬

Evie's Warriors's photo.

 

 

New study underscores how messed up “garbage processing” in neurons causes major problems

TOP DOWN MRI SCAN - Free MSNEW STUDY UNDERSCORES HOW MESSED UP “GARBAGE DISPOSAL” PROCESSING IN NEURONS CREATES BIG PROBLEMS: Breaking the brain’s garbage disposal (AUTOPHAGY): Study shows even a small problem causes big effects: http://medicalxpress.com/news/2016-01-brain-garbage-disposal-small-problem.html (1-26-2016)

 

Messed up cellular “garbage disposal system” found to play a role in Alzheimer’s disease (And Nova Cell’s BEACON FACTOR coaxes lysosomes to do their job!)

Many neurodegenerative diseases involve a failure of lysosomes (the “garbage disposal” system within cells including neurons) to do their job properly. Now comes evidence that defective or compromised lysosomes may contribute to Alzheimer’s disease, something ably laid out in a 6-30-15 article on the Medical Express website at http://medicalxpress.com/news/2015-06-failure-cells-garbage-disposal-contribute.html. Here is a salient quote from this article:

Lysosomes, the “garbage disposal” systems of cells, are found in great abundance near the amyloid plaques in the brain that are a hallmark of Alzheimer’s disease. Scientists have long assumed that their presence was helpful—that they were degrading the toxic proteins that trigger amyloid plaque formation.

However, in Alzheimer’s patients, these lysosomes lack the ability to do their jobs properly, and instead of helping, the accumulation of lysosomes may even contribute to the disease, Yale University researchers report the week of June 29 in the Proceedings of the National Academy of Sciences.

The new findings raise the possibility that coaxing lysosomes to do their jobs could help to prevent the toxic processes that eventually destroy the minds of Alzheimer’s patients.

The big question is how to get lysosomes to do their job as they should. While medicine has little that can pull this off, Nova Cells possesses an effective, nontoxic way to do so: Namely its  proprietary Beacon Factor. Not surprisingly, many patients with neurologic diseases and conditions that involve fouled up lysosomes have responded quickly and beautifully to intravenous infusions of the Beacon Factor. Click to read some of the case histories.

http://www.pnas.org/content/early/2015/06/24/1510329112

A SAMPLING OF PATIENTS WHO BENEFITED AFTER HAVING THEIR CELLULAR “GARBAGE DISPOSAL” UNITS (LYSOSOMES) REVED UP BY THE BEACON FACTOR & PRIMED STEM CELLS

Jane from the “Show Me” State of Missouri – Older lady with Parkinson’s disease & Lewy Body Dementia

Canadian Lady with Progressive Supranuclear Palsy, Corticobasal degeneration (CBD) and prefrontal dementia has an amazing response to her NCIM treatment

“Stem cell treatment gives local family new lease on life” (St. Albert Gazette, Canada)

How Arthur Rechlo regained ground lost to Alzheimer’s cousin

Nova Cells Institute Makes Lewy Body Dementia Breakthrough!

 

IMPORTANCE OF STEM CELL HOMING: https://ncimx.wordpress.com/?s=homing

 

FREE ADVICE ON PREVENTING & REVERSING MENTAL DECINE FROM NOVA CELLS INSTITUTE DOCTORS:

Tips for preventing & reversing cognitive decline & dementia from Nova Cells Institute doctors

 

Nova Cells has assembled information on its stem cell medicine program including stem cell priming and its proprietary Beacon Factor in e-book form titled  “Heroic Medicine” which is free at http://www.novacellsinstitute.com/pdf/Heroic%20Medicine.pdf

Jane from the “Show Me” State of Missouri – Older lady with Parkinson’s disease & Lewy Body Dementia

MRI OF BRAIN - FREE MORGUEFILENote by Nova Cell’s patient educator & care facilitator, Grace Odgers, Ph.D. cand., concerning Jane at the time she was picked up for transport to Mexico plus a brief summary of what took place after her Beacon Factor & stem cell treatments:

Jane arrived seated in a wheelchair with both hands and arms shaking, the left more so than the right. I knew from her history that she was no longer able to walk without assistance. Her son and her partner kind of lift and drag her from her wheelchair to other seating. She is incontinent and thus uses adult Pampers. Very thin ones. She came to treatment accompanied by her live-in partner and her son, both of whom are named Paul. She is given to having occasional hallucinations and is not aware of what is going on around her.

Jane was given large doses of the Beacon Factor by IV drip the first day in hospital. At night she asked to be helped to the restroom. Her partner and son helped her though she walked to the bathroom, and was not dragged.

The day after her stem cell infusion by both spinal tap and IV, Jane became more alert and began looking at her partner and son directly and was conversing with them. She didn’t say a whole lot but she was definitely more aware of everything and everyone around her. She even said “What is going on?”

Notes made by Jane’s son Paul and sent to NCIM:

Jan 20, 2016

1 pm PST, drove down from San Diego to TJ by biochemist Dr.  Abel Pena and Grace Odgers.

Checked into the hospital

3 pm PST: She ate some soup with lime Jell-O.

4 pm PST: The doctors put in an IV and began a saline drip. Mom took her usual medication.

5 pm PST: The doctor added the first dose of “The Beacon Factor”. We ordered dinner, tuna fish sandwiches, mixed fruit with bananas, mango and apples, some apple juice and water.

Mom seem to perk up while eating a lot, offering food to her partner and I while discussing how good she felt.

Tested her memory several times, which was still spotty, but she seemed concerned that she was “failing”.  Noticed that she had her eyes wide open and answered questions quickly, even though sometimes she didn’t make a lot of sense.  We both noticed she had more coherent thought processes and conversation.

7 pm PST: Mom took her final medication of the day.

Jan 21, 2016

6:30 am PST: Arrived back at the hospital. Mom was a bit frantic.

Really need an interpreter the whole time.

Changed bedding and dressings.

7:00 am PST: Mom was given her morning meds.

Took Mom to the restroom.

9:00 am PST: Mom seemed much more lucid, looking around.  Finally started to fall back to sleep after eating.

Changed bedding again and her dressings.

She slept until 11:30 am

1 pm PST: Anesthesiologist arrived and introduced himself and the fact he would be giving her a local in her back for the spinal puncture stem cell injection procedure.

2pm – 3pm PST: Talked with Mom who sat up on her own a lot, looked around a great deal, though she was still hallucinating and engaged in some nonsensical talk. Observed what was going on, and looked forward to going home.  During conversations she started in with “Come here doggie” and “There’s an old woman, really old, scary, staring at me”

Mom’s facial expressions became much more expressive. She was picking her lips and began folding her blankets and fidgeting a lot.

3 pm PST: The MD arrived to check her blood pressure, heart and blood oxygen level.

3:30 pm PST: Still waiting for them to take her in for her infusion.

She’s asking lots of questions and thinking very clearly after all the “Beacon Factor”.

4:00 pm PST: Mom left to go get stem cells.

5:20 pm PST: Mom was returned to the room, still very groggy from the anesthesia but doing well.

6:00 pm PST: Mom exhibited nearly normal behaviors (for her) of obsessing, and mumbling, but without leaning over as she usually did.  More eye movement and she was more concerned over recent events.

8:00 pm PST: Final dose of regular medicines for the day, after which she quickly became very groggy and tired.

9:00 pm PST: Returned to hotel room

Friday Jan 22, 2016

Returned home to Missouri after a day of travel.

Noticed several things, including obsessive behavior though not as extreme. Mom could be easily instructed to lean back, and she looked through the pages of magazines without tearing up the pages as she’d done in the past.  During changing, she lifted herself up as instructed.  Much more focus than before and she kept up conversations on current topics longer than had been true previously.

 

A list of conditions Nova Cells Institute has successfully treated

NOVA CELLS INSTITUTE NEWSCAST - August 8, 2015Learn more about each of the disorders below by either following the link, or emailing or placing a call. Nova Cells has successfully treated many other conditions so if you do not see your particular challenge here, just ask us about our experience with it!

ALS (Lou Gehrig’s disease) – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410

Autism – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410

Cancer Cancer (End-stage & advanced too): http://www.novacellsinstitute.com/cancer-stem-cell-therapy.html

Cardiovascular: https://ncimx.wordpress.com/category/reversing-blockage-in-blood-vessels/

Cerebral Palsyhttps://ncimx.wordpress.com/?s=Cerebral+Palsy

Chronic Fatigue Syndrome (CFS) – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410 

Dementia/Lewy Body Dementiahttps://ncimx.wordpress.com/?s=Dementia

Epilepsy/Other Seizure Disordershttps://ncimx.wordpress.com/?s=Seizure

Fibromyalgia – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410 

Fibrosis – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410 

Multiple sclerosishttps://ncimx.wordpress.com/?s=multiple+sclerosis

Parkinson’s Disease – See alzheimer’s-dementia

Spina Bifidahttps://ncimx.wordpress.com/?s=Spina+Bifida

Spinal Cord Injury/Paralysishttps://ncimx.wordpress.com/?s=spinal+cord+injury

Strokehttps://ncimx.wordpress.com/category/stroke/

Traumatic Brain Injury – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410 begin_of_the_skype_highlighting 

Arthritis & vertigo turnaround in 85 year old lady from Nevada (USA)

Senior Couple At HomeIn later 2014 eight-five (85) year old Patricia Rodriguez went to Mexico to have her longstanding arthritis treated by Nova Cells Institute. During her one day stay she was given umbilical cord stem cells that had been primed to become cells that fight arthritis and promote healing and joint restoration, along with the Beacon Factor.

Upon her return stateside, the very next day Patricia noticed a surge of energy and strength upon walking. However, week after week   positive things of all kinds began surfacing. Her  daughter, Tina, summarized these for Nova Cells as follows:

She has incredible strength in comparison to what was true before (her treatment). She can walk all over Walmart and then when we went to a mall near her home she walked the entire length of it not once but twice, and was only a little tired when we got back to her house”, although, I was tired too.

Tina added, “She can get up from the rocking chair without my daughter having to pull her up. And she can open a can of soda using a finger that could not bear doing this last year”. This was one month after her treatment.

“Also, …and this is the latest thing,…for 48 years Mom had incredibly bad vertigo if she laid on her right side which did not happen when she laid down on her left side. She often said her vertigo was like having the room spin at one hundred miles per hour. Naturally when she slept she made every effort to sleep on her right side. Then last week she woke up on her right side and was absolutely shocked to find she had no vertigo. It has not returned!”

Four months after her treatment she had no arthritis pain, in her hands and right arm, whatsoever.

“Mom was also always afraid of losing her balance. She never fell, but she felt that she might one day do so. She would instinctively grab the rail to go up the stairs in her home and also in mine, and then slowly, cautiously take one step at  a time. She would hold onto the rail and moving up it by taking one step and at the same time moving her left hand over the right hand. She never would let one hand go until she had the other on the rail.”

“Now 5 months after her stem cell treatment she goes up the 15 stair staircase without holding onto anything.”

Nova Cells Institute Mexico offers free case evaluations which people can take advantage of by going to http://www.novacellsinstitute.com/how-to-submit.html

Call 1-562-916-3410

Email NCInfodesk@gmail.com

Why people are flocking to Nova Cells

NCIM SCREENSHOT MARCH 2015Among the many things that draw people to Nova Cells Institute Mexico:

► It’s treatments are effective: NCIM’s use of primed adult (nonembryonic) stem cells along with its proprietary Beacon Factor has brought about swift neurologic improvements in not only adults but also in more than 95% of the children treated to-date. Many children with poor circulation and movement in their lower limbs have experienced the “pinking up” of cold, often oxygen starved (cyanotic) bluish tissue within hours of their treatment often followed by being able to move previously immobile toes, feet and even legs. Many parents with cell phones or video cameras in-hand have excitedly videotaped their children doing things with their bodies they previously could not do within hours of their NCIM treatment. Many of these videos or links to them are posted on this website at: http://novacellsinstitute.com/spina-bifida-updates.html

►Affordability (aka value for money invested in care): Patients, parents and others never have to deal with middle men, brokers, professional marketers or the like when it comes to Nova Cells Institute Mexico. NCIM was founded, in fact, by a group of people who wanted to create a business entity that puts people above huge profit margins. The steadfast refusal of NCIM to retain brokers or other professional sales or marketing people coupled with its dogged pursuit of cost savings in its lab and among its contracted doctors clinics & hospitals has made it possible for NCIM to consistently offer its patients treatments that run well below market. For instance, while many private clinics and hospitals doing stem cell therapies in Asia and China charge $35K USD or more to treat spina bifida children, cerebral palsy, Traumatic Brain Injury (TBI), and such, NCIM typically charges $15-17K USD (Roughly 50% less). In addition, 99% of NCIM neurologic treatments are done in a single day while some being done in Asia and elsewhere can take weeks on end to complete.

►NCIM’s Personal Touch: Nova Cells Institute Mexico was founded and is staffed by caring people who have devoted their lives to relieving suffering and effecting healing. When people call or email Nova Cells they typically have their call or email answered by Grace Odgers, Ph.D. cand., who delights in fielding questions and “filling in the blanks”. When questions or issues are raised that require input from a doctor or scientist, Grace quickly obtains this and passes it along. As part of NCIM’s “personal touch” philosophy, Grace and her husband, biochemist and NCIM director of laboratory Services Dr. Abel Pena, typically help out with getting NCIM patients and their family or caregivers to and from Mexico, and support them through every step of the treatment process while there. If you look closely at the many patient tendered articles on this website and on Facebook and other websites, you will often hear about how Grace and Dr. Abel “have became like family to us”.

And, unlike so many stem cell treatment programs, patients are not treated and turned loose. They invariably get follow-up emails and/or phone calls from NCIM staff especially Grace.

►NCIM Goes the Extra Mile: Nova Cells Institute Mexico primed stem cells, Beacon Factor, donor granulocyte therapy (for cancer) and other treatments have proved to a healing Godsend to so many people in and of themselves. However, this is not all there is to it. NCIM affiliated doctors plus experts in scientifically-validated therapeutic diets, nutrition, herbal medicine and more carefully review patient medical records and test results to determine what (if any) can be recommended that is likely to optimize healing and/or other aspects of the patient’s recovery and restoration, e.g., physical, cognitive, mood, etc. These are then passed on to the patient by NCIM doctors.

And, last but not least……

Nova Cells Institute Mexico offers free case evaluations which people can take advantage of by going to http://www.novacellsinstitute.com/how-to-submit.html

How Arthur Rechlo regained ground lost to Alzheimer’s cousin

NCIM N SIGN - JULY  2013Lewy Body Dementia is sometimes called “Alzheimer’s cousin”. Like Alzheimer’s it is an incurable brain disease that steadily whittles away most sufferers’ cognitive functions including their ability to focus, sleep well, or walk normally. Those with advanced LBD may have trouble swallowing liquids and solids.

Currently LBD affects about 1.4 million Americans. Both radio and TV personality Casey Kasem and Oscar® winning actor Robin Williams had LBD, and legendary Chicago Blackhawks coach Stan Matika was recently diagnosed with it.

LBD has no cure and the best medicine can presently do is relieve symptoms and alleviate patient suffering. The one thing doctors never see is a person with advanced LBD who can hardly walk or talk begin doing so. This all changed after 76 year old Canadian Arthur Rechlo had an experimental treatment in Mexico.

Click to read all about Arthur’s amazing turnaround.

Nova Cells Institute Makes Lewy Body Dementia Breakthrough!

NCIM L.B.D. BREAKTHROUGH ANNOUNCEMENThttp://www.novacellsinstitute.com/LBD/Nova%20Cells%20Institute%20(NCIM)%20Announces%20Lewy%20Body%20Dementia%20%20%20Breakthrough.pdf

LBD NEWS RELEASE WITH PHOTO - ONLINE PR MEDIA - FEB 2015

2-17-15 news release at http://www.onlineprnews.com/news/554299-1424179477-nova-cells-institute-announces-lewy-body-dementia-breakthrough.html/preview

PR UNDERGROUD RELEASE ON LBD - 2-18-15

2-18-15 news release at http://www.prunderground.com/nova-cells-institute-announces-lewy-body-dementia-breakthrough/0053956

Many “giant steps” for Dani

NCIM N SIGN - JULY  2013Danielle “Dani” Smith was born in September 2006 with spina bifida in which her spinal cord did not completely form and resulted in partial paralysis from the waist down (Myelomeningocele). Since then this brave little girl has had five major operations including one to place her spinal cord back in her body, three brain surgeries, and double eye surgery. She then did two stem cell treatments and has undergone lots of physical therapy. And, during June 2013 she was treated in Mexico by Nova Cells using primed stem cells and its Beacon Factor. This treatment and Dani’s responses are reflected in this news release from October 2013: http://www.24-7pressrelease.com/pdf/2013/10/05/press_release_364003.pdf

Dani has made many gains during the year since that news release was published including, most recently, something captured by her mother in a short video. This clip was inserted in an animated video which can be accessed by going to https://www.youtube.com/watch?v=RUBvyFt0Vm4#t=109 or click the screen image below,

 

 

Facebook video & written update by Kara Underwood on her son, Bryson

Kara Underwood

Walking on the treadmill for the first time in his life! He’s in a harnessing system and only has braces from the knees down! We were told he would NEVER in his lifetime do this! All I have to say to every doctor that said NO and he CAN’T and he NEVER WILL is this…….we serve an awesome mighty God who says my son WILL WALK! He promises healing to all who ask for it as we receive it for our son in the name of Jesus!

Ryan Weber (Anoxic Brain Injury): Improvements began surfacing right after his treatment!

To Grace & All The Nova Cells Family:

Sorry for not getting back to you sooner but it has been crazy busy. Mexico was great, nothing we imagined. The hospital where Ryan received his Stem Cell Treatment was so clean and I have been in many different hospitals here in the United States that was not as clean. We enjoyed the Mexican food as it was so flavorful. It made me sad to leave.

Ryan’s Stem Cell treatment was a great success! We noticed a huge difference in his muscle tone when they brought him back from the O.R. I cried when I first picked Ryan up because it was like holding a different kid. Ryan’s muscle tone is completely relaxed. Ryan has started back up with his outpatient physical therapy, warm water therapy and his massage appointments. His therapist were shocked at the difference in his muscle tone. Ryan has more control over his muscles.

Some of the things Ryan has done since his Stem Cell Treatment that he was not able to do before hand include:

HEAD CONTROL -He holds his head in a neutral position now and freely moves it to the left and right to look around. Before Stem Cells, Ryan would either have it tilted to one side or the other or front or back.

Weber 1

Picture taken the day after Ryan’s treatment at the San Diego Zoo. Look at how his arms are more bend, his legs are bend, head in right position. Ryan is actually sitting on the tusk.

HANDS – Ryan is able to open and close his hands freely. He regained the infant grasp reflex. With this he is able to reach out and grab items. Last night (8/26/14), he reached up and grabbed his Dad’s glasses and the later in the night he reached up and grabbed a handful of my hair. Before Stem Cells, Ryan kept his hands closed in a tight fist.

Weber 2

Picture of Ryan’s hands after his Stem Cell treatment

ARMS – Ryan actually is able to control both his arms equally. He is able to bend both elbows at his choice. Ryan is able to control his arms to reach to get items he wants. He still favors the left arm over the right but he was left handed dominant. Before Stem Cells, Ryan did have minimal control over the left arm and no control over the right arm.

Weber 3

Rick and Ryan at the beach before Ryan’s Stem cell treatment. Look at the stiff straight arms and tight closed fist hands

TRUNK (TORSO) – Ryan is able to sit in upright position on our lap with little help. When Ryan sits his chest and belly are straighter. Before Stem Cells, Ryan sat on our lap and needed a lot of help to stay in upright position and usually was tilted to one side or the other.

LEGS – Ryan legs are able to bend at the knees. He is able to control them better alternating them to walk in his walker and today walked in the pool with very little help by himself without a walker. When Ryan sits on our laps Ryan will bend his knees and sit like any other “scientifically Normal” child. When he lays on the floor he will pick up his legs to reposition them. Before Stem Cells, Ryan legs were mainly in a locked straight position. It was a battle to have him sit on our lap, put him in his car seat or in anything that required him to be in a bend position. He would walk in his walker but his body looked like an “S”.

MENTAL – Ryan is happier; he smiles and laughs more. I credit the Stem Cells as he is not always having to deal with very tight muscle which were probably really sore. When Ryan looks at you, he just smiles like he can actually see us clearly. Before he recognized the important people like his siblings, Grandparents and us as his parents but since his Stem Cell treatment-couple of our friends have talked to Ryan and this time Ryan interacted with them.

Most of Ryan’s improvements have been “small” but when you put all the small pieces together it makes for a huge improvement. It’s the little things that matter. I have to tell you a story about our day before we were picked up to go to Mexico.

We were all around and waiting for the phone call to tell us you were on your way. We were sitting outside at the patio set when I opened my pictures in my Phone to find the Creative Miracle Prayer I wanted to say before Ryan’s Stem Cell treatment. My phone usually opens to the last picture taken but that day when I opened my pictures, I started to cry because it automatically opened to a picture of Rick holding Ryan the day he was born back on 12/17/09 (See below). Rick asked what was wrong and I turned my phone to show him the picture that popped up and his jaw dropped. This is the picture that popped up.

Weber 4

I took that as a sign from above that Ryan would be born again. With all of Ryan’s improvements that is exactly what happened! We cannot thank you all enough for making this miracle happen for Ryan. I will send pictures in another email with little explanations of them. Just wanted to get this email of Ryan’s improvements to you. You may share this with everyone and if they want to follow Ryan his Facebook page is www.facebook.com/littlewarriorryan.

Thank you for giving us our little boy back! Lots of love.

Gina & Rick Weber

Tatyana Kushniryuk shares wonderful news about her son Rowan’s response to treatment (Spina Bifida)

2014-03-19 14.28.35My son Roman was born with Spina Bifida in 2010. He is a L4-L5 level which means he cannot void on his own and does not have bowel control. His legs were very weak and he could not walk independently until he was 2.5 years old. He was able to hold on to a walker and push it slowly but the big change came after stem cells. He received his first stem cell treatment in China, and in Mexico twice since then. The latest change was from Mexico.

We arrived to San Diego a few days before treatment and checked into our hotel downtown. The next few days we spent exploring the city and taking a trip to the San Diego SeaWorld courtesy of Warrior Families Beating Spina Bifida Foundation. Roman really enjoyed that trip because he got to see the sea lions and pet the little sharks. He was not as excited about Shamu as I was.

IMAG0225

The next day we were escorted to Mexico across the border with Grace and Abel Pena. They were really great and picked us up in their car and drove us to the hospital. The staff greeted us as we registered in as patients, signed some papers and answered questions about his blood type etc. I can understand how some people may be cautious signing things and giving consent to doctors in a different country but since I knew Grace and Abel from our previous trip to Mexico, I was at ease.

The doctors and nurses were very accommodating and made sure we were comfortable with our room and the procedure. It was much faster than I remember it the first time. The anesthesiologist and doctors talked about how they would only put him to sleep for a very short time and not keep him under sedation when not necessary. They had performed the spinal taps many times and knew their jobs very well. I felt confident in their care and did not have second thoughts about the procedure. I only wish that Roman cooperated as well as I thought he would. He did not like the taste of versed (the relaxing serum before procedures) so we opted to take him without it to the procedure room. The hospital has the coolest stair case that has a slide like side so they can transport people in a wheelchair up and down the twisty ramps.

During the procedure, Grace and I went to eat at a local place so that I would not be nervous and we hurried back because Roman was not going to be in the procedure very long. After we came back, Roman was not awake yet but was brought in soon after. He did great; there was no pain in his back or the IV. He was a bit freaked out thinking that the procedure was just beginning after looking at his IV. It took a while to convince him that we are all done.

After about half an hour, he began eating everything, and I mean everything he could get his hands on. The Jell-O, the rice, the juice, the fruit cup. We had asked for refills. He was feeling really great; He said “Is this Mexico? I like Mexico”…while he’s eating and watching Netflix on our laptop. (by the way, wifi works there and I would take a laptop with Netflix if you have it.)

We had a great experience and soon after we left back across the border to our hotel room. We stopped on the way while Grace and Able treated us to some local cuisine of ice cream, then sandwiches while walking around the outside mall.

Since the trip we have noticed Roman waking up in the middle of the night saying he feels his butt more and that he has to go pee. One day after about 1.5 months he had a wet diaper. He has never had a wet diaper in 6 years! Since then his recurrent infections suddenly stopped and he has been having more strength in his legs to run and walk without his AFO shoes. I am excited seeing these results they are truly worth it! The peeing is becoming more consistent and we are seeing good results in his muscle strength as well.

I encourage anyone that wants to give their kiddo a chance to improve their life to take a chance and make this trip happen.

Tatyana Kushniryuk

2014-03-19 14.23.29

 

VIDEO UPDATE: Bryson Chailer walking without braces!

Kara Underwood posted this video of her son, Bryson, walking without braces to You Tube on Thursday, 7-24-2014: https://www.youtube.com/watch?v=yIr5DJygq6k&feature=youtu.be

Bryson Chailer has some a long way thanks to faith, therapy and, yes, stem cell medicine! 

If you are not acquainted with Bryson’s story here is a link to an earlier Nova Cells Institute blog entry that contains information, links, photos and more: http://ncimx.wordpress.com/2012/05/06/bryson-chailer-rapid-impressive-improvements-in-child-with-spina-bifida/

Bryson & Kara

Photo of Bryson with his Mum, Kara Underwood, taken during December 2013  

Dryden Corvers parents share their Nova Cells experience

Dreaming for Dryden shared a link.
41 minutes ago – 4 pm CDT on June 4 2014

STEM CELL INFORMATION!!!

I have received SO MANY emails requesting information on the stem cells. I would LOVE to talk to each and every one of you personally (and don’t mind doing so) but I do get extremely busy and that often leaves me very forgetful!

I am posting this and pinning it to the top of the page so it is easily accessible.

NOVA Stem Cells Institute (website below):

Yes, it is in Mexico. NO, it is not scary!! The stem cell treatment was done at the women and children’s hospital in Tijuana. The doctors and nurses were very nice and accommodating. It was pretty much like any other hospital. Private room, TV, etc. I will say, the doctors and staff from NOVA speak English… the nurses at the hospital don’t. Just to give a heads up.

The website for NOVA has tons of information, photos, videos, testimonials, etc. You will be dealing with Grace Odgers for information and such at NOVA. Her email is gracepatients@gmail.com and she will GLADLY answer any questions that you may have. If she can’t she will get it.

Our experience was absolutely wonderful. As concerned parents, we left our hotel in San Diego and agreed that if anything felt off, or if we were uncomfortable, we were leaving. No questions asked. But we never had that moment. The procedure is quick, and we were only in Mexico for 3-4 hours at most.

If you have any other questions, please feel free to contact me. As far as progress, browse through Dryden’s page – everything is updated almost daily.

If you do talk to Grace, be sure to tell them that DRYDEN sent you!

Lots of love and GOOD LUCK!!!!!

http://www.wwltv.com/story/news/2014/09/05/14707334/

See More

Nova Cells Institute Mexico Cancer Stem Cell Therapy Treatments
Nova Cells Institute Mexico Cancer Stem Cell Therapy Treatments, NCIM treatments for Spina Bifida, Multiple…

The “why” that motivates & empowers the NCIM family

 

The doctors, administrators, consultants, researchers & ideas people who are part of the Nova Cells family get up each and every day with a single focus & passion:  To find & create new & better ways to bring about healing & restoration.      

HelpingHand

New video: Alejandra crawls on!

 

May 2014 -new Alejandra video: https://www.facebook.com/photo.php?v=613377255426056

Alejandra’s Mum reports: It has been 8mos since Alejandra’s first stem cell treatment and look how she is crawling today Exciting, can’t wait to see what the next one will do! I must give some credit to The March of Dimes, Conductive Education too…for isolating each leg movement independently from the other.

October 12, 2013 blog entry on Alejandra: http://ncimx.wordpress.com/2013/10/12/2-new-videos-of-little-alejandra-spina-bifida-reveal-impressive-progress/

NOVA CELLS SUN GRAPHIC - JULY 2013

NEW video: Dryden Corvers shows off his physical and motor prowess!

Dryden Colverhttps://www.youtube.com/watch?v=k4x7LdrM3vU&feature=youtu.be

“Dani Smith Walks” – You Tube Video update

NOVA CELLS SUN GRAPHIC - JULY 2013Dani Smith walks – 4-7-2014 You Tube video:  https://www.youtube.com/watch?v=YnOGxz2CCMY&feature=youtu.be

Read about Dani in this NCIM blog entry: http://ncimx.wordpress.com/2013/10/05/ncim-pioneering-science-old-fashioned-caring/

Dryden Corvers (spina bifida) continues to make progress!

Dreaming for Dryden

April 5, 2014

It’s been one year since we started this page and started fundraising for Dryden’s trip to NOVA Cells. One of the best decisions we have ever made. Dryden’s new favorite activity is trying to climb. He was climbing up Sissy’s step stool, climbing up the side of the recliner, just wanting to be higher. We are so thankful to everyone who helped make this happen. And so appreciative to NOVA cells for this opportunity. I hope in time this will become a more available treatment. We are certainly going to try again!

Dreaming for Dryden

April 6 2014

He’s a climbing machine!!

 

Photo: He's a climbing machine!!
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Dreaming for Dryden

April 6, 2014

Crawl baby, crawl!!!!! Dryden is now saying (vocally) puppy, baby, mommy, daddy, cookie, cracker, nanny, pawpaw, papa, sissy… I may be forgetting something here but… He’s all of a sudden bursting with vocabulary.

 

 

 

Photo: Crawl baby, crawl!!!!! Dryden is now saying (vocally) puppy, baby, mommy, daddy, cookie, cracker, nanny, pawpaw, papa, sissy... I may be forgetting something here but... He's all of a sudden bursting with vocabulary. :)

 

 

Dryden Corvers (spina bifida): Quick, exiting response to his Nova Cells treatment! (4 days, 2 videos)

Dryden Colver

Dryden is a cute, charming little boy with spina bifida who received primed stem cells & NCIM’s proprietary Beacon Factor on 3-28-14. The entries below are from Dryden’s Facebook page.  

Dreaming for Dryden

March 28

Whew! Long day. We are back at the hotel!!!
Everything went smoothly and we are already seeing some positive results! His feet definitely have better circulation – they are all punk and warm instead of splotchy and cold!

He has been twitching a LOT in his lower legs/feet. This means the nerves are starting to make some sort of connection to his brain. He even moved his left foot and toes when we asked him to (I’ll get video to you in a bit!)

Also – a funny tidbit – he was sitting in my lap and apparently had gas. Those of you who know Dryden know that’s pretty common. What was funny was that every time he would fart, he would look down, look at me and point to his belly. Ha ha! He’s gaining some sensation somewhere new with that too, I suppose!

CLICK TO WATCH A VIDEO OF DRYDEN TAKEN SHORTLY AFTER HIS NCIM TREATMENT

Dreaming for Dryden

April 1

We got back in tonight and stopped in at Dryden’s great grandparents to say hello. Dryden was on the floor and we were all talking. We looked down and he was on his hands and knees CRAWLING!!!! He only went a little ways, but he was very much so 4 point crawling!!! Then as we were sitting there talking about him, he pulled up onto his knees all by himself on the coffee table! Little dude is getting some strength or making some connections – either way – I’m so happy!!!!

CLICK TO WATCH A VIDEO OF DRYDEN TAKEN SHORTLY AFTER HIS NCIM TREATMENT

 Dreaming for Dryden

April 3

Dryden is just continuing to amaze me.

I forgot to mention the other day when we were at his great grandmas that he tried climbing the stairs! Never even noticed them and he was going up!

This morning in therapy he tried crawling a little bit too – but did something even more amazing. He got to his big cube toy and tried pulling up. Not just to his knee either!! She asked him if he wanted to stand up and he said YES!!!! We helped him get his feet secured and he stood there for a short little time playing! Baby steps!!

First time he has ever WANTED to stand!

CLICK TO WATCH A VIDEO OF DRYDEN TAKEN SHORTLY AFTER HIS NCIM TREATMENT

 Dreaming for Dryden

April 4

Dryden wasn’t quite as excited to stand this afternoon, but we made him anyways!
This is him standing up with NO BRACES on!!!

His PT even said she could feel his muscles in his FEET working when he would stand! His ankles didn’t roll or fall out from under him either!

I can only hope that with therapy he will have increased progress!!

Definitely going to be saving for another stem cell treatment in the future!

See More

The Rikky Foresman saga continues: “Rikky is standing!”

Blazin for Rikky – March 3, 2014

https://www.facebook.com/BlazinforRikky

Rikky is standing!!!

Rikky is standing - March 3 2014

READ MORE ON RIKKY FORESMAN AT http://ncimx.wordpress.com/?s=Foresman 

The Angel Sosa saga continues: 24 days without a tonic seizure and counting!

Angel SosaCHECK OUT THIS EXCITING UPDATE POSTED ON ANGEL SOSA’S FACEBOOK PAGE (3-3-2014) 

Since having done stem cells February 6, angel went 24 days without a Tonic seizure!! Before stem cells he was having them everyday 2-4 a day. It only lasted a couple seconds and recovered great afterwards. And with the cluster of infantile spasms some days it seems like there’s none and other days he will have 1-2 maybe lasting only a couple seconds and before he was having 2-4 clusters a day lasting 6-10 mins everyday!! I have also completely weaned him off zonegran his last dose was February 28. So now he’s only on 2 meds depakote and felbamate.

https://www.facebook.com/angel.sosa.52?fref=ts%20

YOU’LL FIND AN EARLIER ENTRY ON ANGEL AT http://ncimx.wordpress.com/2014/02/16/epilepsy-turnaround-for-an-angel-angel-sosa/

Central sleep apnea episodes fall from 66 per night to 7 in Ryan Neighbors, reports mom (Shelly)

Ryan Neighbors - 1 of 4 - January 2014IN A FEB. 10 2014 EMAIL TO GRACE AT NOVA CELLS INSTITUTE, SHELLY NEIGHBORS SHARED THIS EXCITING NEWS ABOUT HER DAUGHTER RYAN: 

I have so much to tell you and show you!

Ryan is moving her legs on her own CONTROLLED!! We’re not walking – but this is a step in the right direction.

Not only that – but she recently had a sleep study to check on her central sleep apnea. Before stem cells, she was having 66 episodes per night. After we Only had 7! They are thinking about taking her off her oxygen!

We hope to see you all again before this fall. I have videos to send but I’m at the gym. I send them when I get home. We love you and hope all is well.

Xoxo
Shelly Neighbors

CHECK OUT THESE PRIOR BLOG ENTRIES ON RYAN: http://ncimx.wordpress.com/?s=Ryan

Epilepsy turnaround for an angel (Angel Sosa)

Angel Sosa is 4 years old and has not exactly had an easy ride in life. Born to loving parents and a large family he entered this world saddled with lots of neurological  and physical challenges. Among them:  Infantile spasms, a  difficult-to-treat form of childhood-onset epilepsy called Lennox–Gastaut syndrome (LGS) or simply Lennox syndrome, and developmental delays. According to his loving Mum, Monique, he was ““having 10 clusters of 10-11 seizures lasting six (6) minutes each day and was having ten tonic seizures a day sometimes lasting up to 3 minutes without breathing.”

As you might expect little Angel’s early life was spent seeing doctors and therapists and taking drugs to control his epilepsy (Three currently: Felbamate, Valproic acid, and Zonisemide). Naturally, his parents kept an eye on the news and the Web for any medical advances that might offer any hope of remediating their son’s intractable epilepsy and other challenges. With the advent and growth of adult (nonembryonic) stem cell treatment programs outside the US they saw evidence that perhaps some form of stem cell therapy could help their little boy. As they sorted through the various private stem cell medicine operations abroad they came across accounts of the many turnarounds in children effected by Nova Cell’s primed stem cell treatments and intravenous use of its proprietary Beacon Factor. This encouraged Monique to reach out to NCIM patient educator & care facilitator, Grace (Ph.D. candidate), by phone. Grace then walked her through what NCIM doctors and scientists had accomplished and documented in treated patients and then ably tackled all her questions and concerns. Satisfied with what she had learned, the Sosa’s, enrolled their son in the NCIM treatment program and read the patient handbook (This link is to the abridged version of NCIM’s patient handbook. Those who wish to access the full version must register). Later, on the heels of Angel’s approval for treatment by NCIM physicians including a pediatric neurologist, she and her husband booked him for care on 6 February (2014).

When the “big day” arrived for Angel, Grace noted this about the little boy:

While waiting for his treatment Angel was very stiff and somewhat arching backward. His eyes were moving around the room randomly and, though he would look at you if you called his name after a couple of times, he did so only for a split second and it seemed that he saw right through you. His mom had to give him his dose of medications because he was getting a little more stiff and she knew they were wearing off.

Angel SosaAngel was then given primed umbilical cord stem cells and the Beacon Factor. Grace noted this at the time:

About an hour after his stem cell treatment Angel’s mom mentioned to us that both she and his father were impressed with how relaxed Angel is including his normally stiff legs. As the attending physician was checking him in recovery Angel did something amazing: He fixed his gaze on him for about 5 seconds. The doctor was both amazed and incredulous. Then Angel’s father said ‘Oh yea, he already has focused  his gaze on his mom and I.’  Within an hour Angel was already aware of his surroundings and the people around him.

In addition, Angel’s legs which were normally ice cold were now pink and warm and remained so.

After Angel got home and settled in Monique shared this with Grace by phone and later by email:

The Thursday morning of his stem cell treatment he had 3 tonic seizures and then after stem cells no more seizures till late Sunday night he had 2 small quick seizures. All this week he’s only had 3 seizures! And no big seizures at all! No more 6 minute clusters 🙂

In therapy his therapists have noticed improvements already! He feels so much stronger! He is tolerating standing a little more and one of his therapists noticed he was using the muscles on his arm and shoulders. Everyone has noticed that he’s more alert and happy and has more energy! On Tuesday he looked at me and smiled Mind you, he has never smiled for no reason.

Monique added that Angel’s three (3) year old sister was super excited by the fact her brother was following her all over the place with his eyes, something she instinctively regarded as a form of playing with her.

She concluded with this:

Thank you NOVA!!! I’m so excited about seeing more gains with my angel! Thank you Grace and Abel!

The Sosa’s have set up a  Facebook page for Angel which is at https://www.facebook.com/angel.sosa.52?fref=ts. This page contains photos, videos, posts and more.

CHECK OUT THIS EXCITING UPDATE POSTED ON ANGEL SOSA’S FACEBOOK PAGE (3-3-2014):

Since having done stem cells February 6, angel went 24 days without a Tonic seizure!! Before stem cells he was having them everyday 2-4 a day. It only lasted a couple seconds and recovered great afterwards. And with the cluster of infantile spasms some days it seems like there’s none and other days he will have 1-2 maybe lasting only a couple seconds and before he was having 2-4 clusters a day lasting 6-10 mins everyday!! I have also completely weaned him off zonegran his last dose was February 28. So now he’s only on 2 meds depakote and felbamate.

GRACE - CLOSE UPWant to know more about NCIM and its stem cell treatment program for neurologic issues in children and adults? Call NCIM’s US information line at 1-562-916-3410 (10 am to 7 pm Pacific Time, Monday through Friday) or email Grace by e-mail at gracepatients@gmail.com.

Do you believe in miracles? If not, read this!

Little Rikky could not feel anything below his knees but started doing so in the first few hours following his Nova Cells treatment! 

POSTED BY RIKKY’S FOLKS ON THEIR LITTLE BOY’S FACEBOOK PAGE ON 1-8-2014 (Link further down below)

Check it out! Rikky had no feeling below his knees prior to the treatment! This is 30 minutes after he came out of the O.R. and we will see results for 6-8 MONTHS!

If you didn’t believe it before when we said it was going work then watch this!!!

CLICK PHOTO TO WATCH THE VIDEO (RIKKY’S FACEBOOK PAGE)

I just want to scream from the freaking rooftops, I am so full of joy and thankfulness! It  exceded whatever I imagined to happen, just seeing hime moving his left leg is giving me chills over and over and over and over again! AND HIS LEGS ARE LOOSEY GOOSEY!EVEN MORE THAN AFTER THERAPY!!!!!!!!!!!!!!!!!!!!!!!

And posted tonight (1-8-2014) from SEAWORLD in San Diego at around 7 pm Pacific Time:

“FEEL MY LEGS, DAD”. So we are sitting watching the dolphin show and Rikky says this because he has shorts on and it’s a little chilly (we all have shorts on btw). He NEVER felt his lower legs before!

And posted to Rikky’s Facebook page on 1-14-2014:

Blazin for Rikky

Went to Rikky’s PT she is amazed at Rikky’s progress from the stem cells! She says it is unbelievable and she is going to write a letter that says how the stem cells worked so well on Rikky. She has been his PT since he was 2 months old, and she has been a PT for over 30 years. She is quite amazed! This makes me quite joyous because she validates what I have been seeing and I know now that I am not imagining things! This is only ONE WEEK after treatment, we will still have progress for 6 MONTHS!! This is so wonderful! Grace and Abel are angels!!! I am so glad we decided to do this! I hope more people will see this progress with Rikky and get this for their kids too! I highly recommend NOVA CELLS INSTITUTE!!! THEY HAVE CHANGED OUR LIVES!!!!!!

POSTED ON 1-24-2014 ON RIKKY’S FACEBOOK PAGE:

Blazin for Rikky

OK, we seriously just went to ER because I haven’t been able to get a catheter in. The ER dr says he is voiding on his own and does not need to be cathed so call his uro Dr and get the tests done to be sure, but he is completely voiding ON HIS OWN!!!!!!

Check out Rikky’s FACEBOOK page at https://www.facebook.com/BlazinforRikky (Videos, posts, comments & more)

 

                  

Update on Ryan Neighbors by her Mum, Shelly (Includes a link to a recent video of Ryan and 4 photos)

New video of Ryan standing ALMOST all on her own:

https://www.facebook.com/photo.php?v=10202462548192683&l=1269382276310712012

We are starting fundraising again this weekend. and our goal is to be back (to Nova Cells) by this summer/fall

Ryan’s core strength is MIND BLOWING. She’s breathing so much better and eating all sorts of different foods. She is also writing her name and is able to stabilize her  trunk and balance when in a crawling position and when standing. Her legs aren’t doing as much as we hoped, BUT she has gained so much strength in her core and in other places I never even thought of it helping her legs. I know for a fact we wouldn’t be where we are today without your help and the stem cells. Hopefully a 2nd round will do much more.

We love you guys and can’t wait to see you again.

GOD IS GOOD. Love you guys MUCHO!!!!

Shelly Neighbors

AND IN A FEBRURY 10, 2014 EMAIL SHELLY HAD THIS TO SHARE WITH NCIM’S GRACE:

I have so much to tell you and show you!

Ryan is moving her legs on her own CONTROLLED!! We’re not walking – but this is a step in the right direction.

Not only that – but she recently had a sleep study to check on her central sleep apnea.  Before stem cells, she was having 66 episodes per night. After we Only had 7! They are thinking about taking her off her oxygen!

We hope to see you all again before this fall. I have videos to send but I’m at the gym. I send them when I get home. We love you and hope all is well.

Xoxo

Shelly Neighbors

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2 new videos of little Alejandra (spina bifida) reveal impressive progress!

Nova’s Cells Institute (NCIM) doctors, scientists and other participants in its ever-evolving stem cell medicine program celebrate each and every improvement that surfaces in the people it treats. What follows below are links to 2 videos of little Alejandra which showcase the truly impressive post-treatment progress she has made. These videos were posted to Alejandra’s Facebook page by her Mum whose comments follow the link to each video.

Join NCIM as it celebrates little Alejandra’s ongoing journey to betterment and her recent improvements!

https://www.facebook.com/photo.php?v=508529795910803 (2 minutes, 38 seconds)

Antonella’s comment about this video of her daughter, Alejandra: 1 month post stem cells…I so wish I had a video of what she was doing before stem cells because you would not believe this progress…THANK YOU NOVA CELLS, MEXICO!

https://www.facebook.com/photo.php?v=508520542578395 (1 minute, 7 seconds)

Antonella’s comment about this video of her daughter, Alejandra This is how she is moving now…only 1 week after stem cells…THANK YOU NOVA CELLS, MEXICO! — at March of Dimes Canada.

 

Quotes from mothers of children treated by Nova Cells


NOVA CELLS - A RIVER OF LIGHT & HEALING with contact & website info - Darker background

Doing the Math: What sets Nova Cells apart from the “rest of the pack”?

Do you wonder what sets NCIM apart from other stem cell medicine operations? We have summarized the major differences in a simple chart which you can access by clicking the image below or by clicking or keying in http://bit.ly/18Sf87t

 

DOING THE MATH

Ryan Neighbors News Release on “The Shine” (Europe’s largest spina bifida charity)

THE SHINE - 9-30-2013On Sunday an NCIM press release on little Ryan Neighbors appeared on 3 PR services (24-7 Press Releases, Fire PR in the UK, and Free Press Release) and in the handful of hours since has created a bit of a positive stir. For one thing, Europe’s largest spina bifida charity picked up on tweets of the press releases and ran them on their main website at http://paper.li/SHINEUKCharity/1319719408. Many parents of children with spina bifida also picked up on the news release as well and one, Kara Underwood, whose son Bryson benefitted from treatment by NCIM, had this to say about Nova Cells on Facebook (Sunday 9-29-2013):

Best place on the planet for all your stem cell needs! They have the most caring team of patient coordinators and doctors around! Love them all to pieces! They are helping so many have a better quality of life! I praise God for Nova Cells Institute! 

Email Kara at karalinunderwood@gmail.com

OLYMPUS DIGITAL CAMERA

Want to know more about NCIM and its stem cell treatment program for spina bifida and other neurological issues? Call NCIM’s US information line at 1-562-916-3410 (10 am to 7 pm Pacific Time, Monday through Friday) or email NCIM patient care facilitator/educator Grace by e-mail at gracepatients@gmail.com.

Blocked blood vessels? Nova Cells has good news concerning reversing it!

If you happen to have PAD or CAD especially an advanced stage (e.g., angina in CAD, severely restricted circulation in PAD), NCIM wants to make you aware of its own advances in this area:

 (1) NCIM’s Beacon Factor given by intravenous means substantially increased the blood flow in both children and adults with impeded circulation including (in adults) blocked blood vessels. It not only did this during the time it was being administered but kept up the better blood flow for weeks and even months afterwards. This, of course, is not a “permanent solution” to PAD or CAD and is not advocated as such. It is, in fact, only used to “get things going”; that is, to improve blood flow short term in order to set the stage for #2 below.

(2) Following a few days of Beacon Factor infusions, patients are given a regimen for reversing arterial blockage; one worked out over many years by one of NCIM’s consulting researchers who first established its ability to reverse arterial plaque in animal models of CAD, and then entrusted it to physicians who utilized it on patients with PAD and CAD, kept track of responses and documented CAD reversal. This regimen has dietary, pharmaceutical and supplement components to it.

For instance, during 2012 the regimen was used by a gentleman with advanced PAD who was wheelchair bound and facing amputation of his lower legs. After 8 months on it this fellow’s MD surgeon declared that his blood flow was such that amputation was “no longer a consideration”.

The NCIM Beacon Factor and special regimen to reverse PAD and CAD is, of course, experimental and as such carries a certain element of risk and is not guaranteed as to outcome. This will be spelled out during the informed consent process.

Each case, of course, requires careful evaluation including a comprehensive records review to determine whether the patient is a suitable candidate for NCIM’s PAD/CAD reversing treatment approach. Those interested in learning more or being evaluated (there is no charge or obligation) should contact NCIM by phone at 1-562-916-3410 from 10 am to 7 pm Pacific Time, Monday through Friday or by email at NCInfodesk@gmail.com

NOVA CELLS SUN GRAPHIC - JULY 2013

Let’s cut to the quick: Why should you go with NCIM’s stem cell program?

Thousands of people have visited this website as part of “shopping” for a stem cell treatment. Many have chosen to be treated by Nova Cell’s after tallying up what it offers. Here is what they have discovered:

  • Nova Cells Institute of Mexico (NCIM) was founded by doctors, researchers and others who have spent years in the “stem cell industry”, some having been a part of it almost from its beginning.   
  • NCIM’s uses adult not embryonic or fetal stem cells, e.g., stem cells from certifiably disease-free stem cells isolated from umbilical cord blood, placental tissues, and Wharton’s Jelly. It also isolates and uses stem cells from patient’s own bone marrow.      
  • NCIM has developed unique, proprietary technology & lab methods that have made it possible to not only to get stem cells to target tissues, but to prime them to respond to chemical cues by becoming specific cell types that promote repair and healing. No other firm anywhere has this.
  • Treatments are done in modern, secure medical facilities in Mexico (Tijuana).
  • NCIM has developed a powerful treatment for advanced cancer, e.g., treating patients with pooled donor granulocytes, which has gotten many cancer sufferers into partial and complete remission. Its doctors and scientists possess a precise protocol for doing this treatment safely, which no other hospital or clinic anywhere has.
  • NCIM’s stem cell-based treatment has proved especially beneficial in people with cerebral palsy, spina bifida, multiple sclerosis, spinal cord injuries and traumatic brain injuries.
  • NCIM’s contracted medical facilities & labs all enjoy approval by the Mexican equivalent of the FDA.
  • NCIM’s Director of Laboratory Services, Abel Pena, was trained by the head of stem cell research for a major R & D company in southern California.
  • The cost of NCIM’s stem cell treatments are typically far less than other private stem cell treatment operations, not only in Mexico but elsewhere in the world.

Your next step? It’s simple, just click this link and then register: http://www.novacellsinstitute.com/register.html (There is no cost or obligation whatsoever)

You can also get more information or ask questions by calling NCIM’s U.S. information line at 1-562-916-3410 or emailing NCIM at NCInfodesk@gmail.com    

NOVA CELLS SUN GRAPHIC - JULY 2013

Multiple Sclerosis: Three recent cases

Mr. J. R. is a 49 year old Mexican national who has been struggling with Progressive Relapsing Multiple Sclerosis for six years, which was rapidly progressing prior to his coming to NCIM (January 2012).

He arrived at NCIM’s treatment facility unable to walk and with his speech so slurred only his family was able to understand him.  He also had difficulty swallowing as well as being unable to move his tongue very well. According to NCIM co-administrator & patient care coordinator, Grace, Mr. J. R.’s arms functioned normally but everything from the waist down plus his tongue and throat did not. He was treated with stem cells derived from three umbilical cords, Wharton’s Jelly and his own bone marrow (primed using Nova Cell’s unique laboratory method) along with NCIM’s proprietary Beacon factor.

Six weeks after his treatment Mr. J. R. was able to be understood even on the phone. He was so amazed and ecstatic with the improvement in his ability to communicate that he could not resist calling people to chat plus family and friends whom he often invited to him home to visit with him.

About three months following his treatment he was walking again, specifically taking a few steps at a time and climbing a few stairs — with assistance.

As of August (2012) Mr. J.R. can walk (slowly) without assistance and can also touch his palate with his tongue. He is hoping to be able to return to NCIM in January 2013 for another treatment.

Ms. Elisa is a 38 year old lady diagnosed with Secondary-Progressive Multiple Sclerosis four years ago. Among the things she has been wrestling with:

  • Poor balance
  • Lots of pain in her legs
  • Rigidity in her hands and one leg
  • Migraines
  • Unable to walk well (Alternates using a walker and wheelchair to get about)
  • Severe depression
  • Poor appetite with corresponding weight loss

Ms. Elisa was treated during December 2011 with primed stem cells from Wharton’s Jelly, cord blood and her own bone marrow, along with NCIM’s proprietary Beacon Factor.  

About two months after her treatment Ms. Elisa noticed her migraine headaches were becoming less frequent. In addition, she was able to balance herself to the point of not being afraid to fall any more though she continues to use her walker to get about. The rigidity in the hand and leg on one side of body has diminished and the other leg is no longer rigid though there is some light twitching which she is managing with tonic water and quinine. Also, Ms. Elisa is eating better, has gained some weight, and though she feels sad she no longer feels controlled by depression (The severe bouts of depression having completely disappeared). She reports seeing no further disease progression.

Mr. M. S., the brother of a prominent Mexican politician, is not a Nova Cell’s patient but instead was treated by his primary care doctor in Mexico using stem cells processed and primed by NCIM. He has been struggling with multiple sclerosis for eight (8) years and complained of severe fatigue, blurred and double vision in one eye, problems with his bladder, constipation, lots of muscle spasticity plus loss of muscle strength.

He was treated in February 2012 and responded so amazingly well his family brought him back to Tijuana in the middle of June to get a booster treatment.

Among the benefits Mr. M.S. has reported:  His spasticity is much better especially following his second treatment, his vision is improving and he is getting more control of his bladder. His family is taking him to physical therapy which has resulted in his gaining some physical strength. Perhaps most impressive of all to Mr. M. S. is the fact that his condition has stopped progressing.  

Mr. M.S. anticipates seeing additional gains in the months to come and has pledged to report any and all changes to Nova Cell’s co-administrator and & patient care coordinator, Grace.

Want to know more about NCIM and its stem cell treatment program for neurologic issues including Multiple Sclerosis? Call NCIM’s US information line at 1-562-916-3410 (10 am to 7 pm Pacific Time, Monday through Friday) or email NCIM patient care facilitator/educator Grace by e-mail at gracepatients@gmail.com.

Gabe Smith (Spina Bifida): Making rapid progress

My name is Kristin Smith and my 2 ½ year old son, Gabe, has myelomeningocele type spina bifida affecting the L3-L4 region of his spine. He also has a VP shunt in place. When he was 1 ½ years old we took him to China for his first stem cell treatment where he received eight (8) intravenous IV treatments with umbilical cord stem cells along with acupuncture, physical therapy, fire cupping and massage. The cost was $30,000 USD. Prior to this treatment Gabe was unable to use his legs and had low hip movement as well as low sensation and poor blood flow in his legs and feet. Following his treatment he was able to move his hips enough to use an RGO brace (which basically supports his legs and moves them once he initiates movement with his hips) that allows him to walk with a walker. In addition, he had greater sensation to his knees and was able to support himself on his knees while holding onto something. He also experienced more sensation in his penis.

In May 2012 we went to Tijuana, Mexico for his second stem cell treatment with Nova Cells Institute (NCIM). We had heard many wonderful things about this group especially with regard to the rapid results that families were seeing in their spina bifida-afflicted children following treatment with Nova Cell’s primed stem cells. At the same time we also heard many negative things about the north Baja area, as I’m sure most people from the States have, e.g., violence, kidnapping, dirty, dangerous, etc. We went despite the rumors and are so thankful that we did! To our surprise Tijuana is very clean, full of nice people and a lot of uniformed young children walking around and playing after school. We ate in a local restaurant around 8 pm and never for a second felt insecure or in any danger whatsoever. It was the opposite of what we were told by well meaning friends and other who were basically just speculated wildly. We had great food and while waiting to cross the border (back into the US) were able to buy some great souvenirs from the local people who were working hard to support their families.

As for the treatment itself, NCIM’s Grace and Abel picked us up at our hotel in San Diego and were simply the best hosts you could ever hope to find. Once at the clinic, our son did not cry when we handed him to the doctor because Abel was in the OR with him throughout the entire procedure which made him feel totally at ease. The procedure went perfectly and his legs almost immediately warmed up (better blood flow) which made both he and us so very happy. Grace stayed with us during Gabe’s treatment and recovery, comforting us and answering all our questions, and then went with my husband to get some food. Amazingly, after they returned with the food our big boy ate an entire plate of chicken and rice thirty. Hardly (30) minutes had elapsed since his treatment!

Within the first week after Gabe’s treatment we began seeing improvements. Among them:

☺He was able to consistently crawl while pulling his legs underneath himself.

☺He was able to climb up 10 stairs without help, pulling his legs up all by himself.

☺ Also, his therapist realized that he was no longer relying on his RGO to move his legs, but was using his own leg muscles to walk!

All of these gains represented firsts for Gabe, mind you.

Now it has been almost two (2) months since our treatment and he is moving his legs from the knee, and has a lot more strength. He has more sensation further down his legs and is a lot faster and more mobile. Also, he is able to move around during play in ways that he never could before.

I would be remiss if I did not point out the vast difference between Gabe’s treatments in China and then Mexico (Nova Cells): The Chinese stem cell & other treatments took place over many weeks, cost $30K USD, and produced some modest physical improvements. The Nova Cell’s primed stem cell treatment took a single day, cost far less than the Chinese treatment, and produced very impressive improvements in Gabe literally coming out of the gate and continuing to this very day.

To say we are all more than delighted with Nova Cells and the wonderful people who make up the NCIM family is an understatement.

Readers should feel free to contact me at kristinsmith32@gmail.com but please put something in the subject line pertaining to stem cells so I do not think it is spam.

JULY 21, 2012 VIDEO OF GABE: http://www.youtube.com/watch?v=u4xsGl926yo&sns=fb (28 seconds)

ADDITIONAL VIDEOS OF GABE CAN BE FOUND BY CLICKING THIS LINK: https://www.youtube.com/results?search_query=mospina85

REGULAR UPDATES ON GABE’S PROGRESS ARE POSTED TO “GABE WILL WALK” ON FACEBOOK: https://www.facebook.com/#!/GabeWillWalk?fref=ts (NOTE: You will need a Facebook account to access this community page. If you do not have a Facebook account you can easily set one up by clicking this link https://www.facebook.com/r.php?locale=en_US)

Want to know more about NCIM and its stem cell treatment program for neurologic issues in children and adults? Call NCIM’s US information line at 1-562-916-3410 (10 am to 7 pm Pacific Time, Monday through Friday) or email NCIM patient care facilitator/educator Grace Pena by e-mail at gracepatients@gmail.com.

Emily Johnson: Ten year old with cerebral palsy turned a corner following her NCIM stem cell treatment

Ten year old Emily Johnson was born 16 weeks premature (weighing in at only 1 lb 6 oz.) and sustained nervous system damage later was manifest as an inability to communicate verbally, problems getting about, and seizures. Her doctors diagnosed her as having cerebral palsy. Like many children with CP Emily benefited from use of a walker and various kinds of therapy. In time her seizures abated and she learned to communicate via a speech device. Her parents, Patrick and Justin, wanted more for Emily, of course. Like most other parents of children with CP they went on a quest for therapies (including novel ones) that might reduce or remediate Emily’s disability and improve or enhance her motor and cognitive functioning. This quest brought them to Nova Cells Institute of Mexico (NCIM) in December 2011 and culminated in Emily’s being treated with pure umbilical cord and Wharton’s Jelly derived stem cells plus “Beacon Factor”, i.e., a proprietary hypoallergenic combination of peptides and cytokines that helps stem cells rapidly home in on and anchor to target tissues (NCIM’s Beacon Factor has been used by NCIM on all types of neurological diseases such as cerebral palsy, multiple sclerosis, spina bifida, and Parkinson’s disease with great success).

Emily’s response to her NCIM treatment began 2 months following her treatment and is ably captured in this update from her parents that came in this month (May 2012):

Our daughter Emily had a stem cell treatment through NCIM when she was 10 years old.  We set up everything through (NCIM patient educator and care facilitator) Grace and she was wonderful to us.  She was so attentive and loving and I really felt a bond with her over the phone and felt like I knew her and could really feel her excitement for helping kids!

When we got to San Diego, Grace and (her biochemist husband) Abel picked us up and personally escorted us to Mexico!  Traveling to another country can be a bit overwhelming but they made us feel at ease and we really felt like they cared about our little Emily and they were very thorough in explaining how they get the stem cells and treat them and the desired outcome.

Since the treatment we have seen some wonderful changes in our daughter.  Emily is non-verbal and cannot walk without assistance.  Prior to her stem cell treatment she could not ask for help or communicate her needs effectively even with a speech output device. Now, just 5 months after treatment, she clearly articulates her needs using the device and she has also learned how to use an iPad for communication as well.

She has also shown a new level of maturity.  She has demonstrated through testing that she can read well over 200 words.  She is also able to build sentences and follow along with academic activities using her speech device.  Her temperament has also changed.  She used to break down easily and get very frustrated and she was unable to control her emotions.  Now she seems to be more patient and confident in herself.

We feel that these changes are just the beginning and we are hopeful and excited to see even more good things coming from her treatment!

TO ACCESS A NEWS RELEASE THAT INCLUDES MENTION OF EMILY CLICK THIS LINK OR GO TO http://bit.ly/J9AKQw

Want to know more about NCIM and its stem cell treatment program for neurologic issues in children and adults? Call NCIM’s US information line at 1-562-916-3410 (10 am to 7 pm Pacific Time, Monday through Friday) or email NCIM patient care facilitator/educator Grace Pena

2nd Patient treated for advanced cancer by NCIM

Croatia Cancer Patient stem cell treatment7-22-11: A gentlemen with advanced disseminated prostate cancer with metastases to the bone flew into Mexico a few days ago (from Croatia) to begin the NCIM cancer-fighting program. He has had 2 treatments to-date and has already experienced his color return to normal and strength return to his arms. The attending MDs and RNs are flabbergasted, as is this fellow’s daughter who flew in with him. Though these are just initial responses they closely parallel those seen in the 1st patient and for this reason have everyone involved quite excited and enthused! More to follow as this chap gets further into his 3 week course-of-therapy.

8-26-2011: The patient returned to his home in Eastern Europe and continues to improve, according to family and close associates. NCIM is now awaiting receipt of a medical assessment from his primary care physician.

1-12-2012: The patient’s daughter sent an email to NCIM indicating that her father has no pain whatsoever and is off of all morphine (He was utterly dependent on morphine to control intractable cancer-related pain at the time of his Nova Cell Institute treatment in 2011.) NCIM staffers are trying to arrange to get a status update from his primary care MD in Croatia.

Spencer Tomc saga continues

If you have not done so please read the “Spencer Tomc” story:  http://bit.ly/n333qh

UPDATE on Spencer sent NCIM on 10-20-2011 from Mrs. (Jennifer) Tomc:

We had an appointment with Spencer’s Neurosurgeon this morning to follow-up on his tethered cord.  His exact words as we were leaving were, “I would chase you away from detethering surgery with a whip.”

Great news for us for sure!  We thank God and each of you for the supplements and therapies and support and information to turn this around for Spencer.  We will continue all of these to continue his healing.