Learn 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
Cerebral Palsy – https://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 Dementia – https://ncimx.wordpress.com/?s=Dementia
Epilepsy/Other Seizure Disorders – https://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 sclerosis – https://ncimx.wordpress.com/?s=multiple+sclerosis
Parkinson’s Disease – See alzheimer’s-dementia
Spina Bifida – https://ncimx.wordpress.com/?s=Spina+Bifida
Spinal Cord Injury/Paralysis – https://ncimx.wordpress.com/?s=spinal+cord+injury
Traumatic Brain Injury – Email NCInfodesk@gmail.com for specifics or call 1-562-916-3410 begin_of_the_skype_highlighting
Linda’s little boy has cerebral palsy and has vision, cognitive and walking issues. Within a week of getting primed stem cells & the nontoxic Beacon Factor by Nova Cells Institute doctors (August 2015), Linda shared this with NCIM’s Grace Odgers, PhD cand. by email (firstname.lastname@example.org):
As you know, my boy has really been struggling for a long time with walking and now after his treatment he just gets up and does it! Today he was even trying to run about. Also, I see signs his vision has improved too. On top of all this, his temperament is so much better and he is no longer easily frustrated and his ability to focus & take on challenging tasks has improved. For instance, today at therapy he put objects like circles, triangles and stars into the right sorting container which left the staff totally blown away! My husband took in all these leaps forward which left him almost in a state of disbelief! I wish all the parents of children with CP would get them into treatment with your program. Warmest regards to both you and Dr. Abel, and do watch your email for more progress updates and video clips too of our boy. Love, Linda.
At the hospital, even before we left to take this family back to their hotel in San Diego, the boy was sitting on the floor, then just folded one of his legs and got right up without help from his mom or anyone present. This so amazed the lady that it left her totally wide mouth open. Then at the hotel the boy did it again but this time took about 4 steps and sat down. The mother was simply awed by what was happening.
Want to know more about NCIM and its pioneering treatment program for cerebral palsy (CP), spina bifida and other neurologic conditions? Then grab your phone and call the NCIM U.S. information line at 1-562-916-3410 or email NCIM patient care facilitator/educator Grace Odgers, Ph.D. cand., by e-mail at email@example.com.
A boy with devastating brain damage due to a near drowning accident underwent treatment with primed umbilical cord stem cells and the Beacon Factor by NCIM. The child’s response was so profoundly positive that his normally reserved father tearfully exclaimed, “How can we begin to thank you for giving us back our son?!?”
If you’d welcome more details 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 firstname.lastname@example.org.
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.
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.
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.
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.
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
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.
CHECK OUT THESE PRIOR BLOG ENTRIES ON RYAN: http://ncimx.wordpress.com/?s=Ryan
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:
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:
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)