The Nova Cells Lifestyle

Ethical stem cells only: placental, umbilical cord, Wharton’s Jelly, bone marrow

Safety: Top notch.

Efficacy: Well established.

Pricing: Below market. No middlemen, marketers, brokers or PR people.

Contracted facilities: modern high-tech hospital near the US-Mexico border. Safe, secure.

NCIM doctor holding patient

Contracted healthcare professionals: MDs and RNs. MDs include internists, diagnosticians, traumatologists, and board certified specialists.

Stem cell treatments: Done mostly by intravenous (IV) means but intrathecal and local injections done if needed/required.

Unique to NCIM: Donor immune cell therapy for cancer; stem cell homing compound “The Beacon Factor“; others.

Support: Pre- and post- treatment support and follow-up.

NCInfodesk@gmail.com, 1-562-916-3410 (US information desk)

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 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 in Mexico getting IV infusion

On 4-27-16 Heather Morgan sent this email message to NCIM:

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

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.

Evie’s Warriors

April 15 at 5:49pm ·

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

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

Note by Nova Cell’s patient educator & care facilitator 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 .

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.

Dreaming for Dryden: Facebook Community Page Update with photos!

https://www.facebook.com/DreamingForDryden

https://ncimx.wordpress.com/?s=Dryden

Many “giant steps” for Dani

Danielle “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,

 

 

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.

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

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/

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

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

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

PRIOR NCIM ENTRY ON DRYDEN: http://ncimx.wordpress.com/2014/04/02/dryden-corvers-spina-bifida-quick-exiting-response-to-his-nova-cells-treatment/

DRYDEN’S FUNDRAISING WEBPAGE IS AT https://www.giveforward.com/fundraiser/m662/dreamingfordryden  

“Dani Smith Walks” – You Tube Video update

Dani 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!!

 

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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.

 

 

 

 

PRIOR NCIM ENTRY ON DRYDEN: http://ncimx.wordpress.com/2014/04/02/dryden-corvers-spina-bifida-quick-exiting-response-to-his-nova-cells-treatment/

DRYDEN’S FUNDRAISING WEBPAGE IS AT https://www.giveforward.com/fundraiser/m662/dreamingfordryden