Stem cell Therapy for cerebral palsy: Dylan Hancock (Mansfield News Journal)

Dylan and Tessa Hancock - Stem Cell Treatments for Cerebral Palsy

Stem Cell Therapy Subjects Dylan and Tessa Hancock with their father, Jeremy

Written by Jami Kinton
Mansfield News Journal

ASHLAND — Three-year-old twins with cerebral palsy are making life adventurous, challenging and bittersweet for the Hancock family.

“They’re happy kids but it definitely makes it more difficult because as a parent you want them to have every opportunity that every other child has,” said mother Carrie Hancock. “It’s hard, but we’re handling it the best we can.”

Because they were born 10 weeks premature, both children suffered developmental delays.

By the time Tessa and Dylan were 20 months old, Tessa had been diagnosed with cerebral palsy, a permanent disorder that affects movement and posture. At that time, parents Carrie and Jeremy were getting ready to take their daughter overseas for a stem cell transplant, a procedure that would allow Tessa to live a better, less physically restricted life.

The results were remarkable…

In the midst of their planning, the family was soon faced with another obstacle. That January, Dylan also was diagnosed with cerebral palsy.

“What do you do? They’re your babies. You just go with it and do what you think is best,” Carrie said. “Before, we were always told that he just had developmental delays, but as much as you hated to hear it, it was almost a blessing because we were paying out of pocket for him because he hadn’t been officially diagnosed.

“That’s the silver lining I guess and now we’re able to get him the help he needs.”

The Ashland family ended up taking Tessa to Panama City, Panama, where she had her first round of stem cell treatments in 2009.

“She did really well and had a lot of improvement with her vision,” Carrie said. “Her tone in her hand had decreased and she wasn’t fisting all the time. When we went back in July, we took both the kids.”

The results were remarkable.

“As soon as we took him, he was like a whole other kid,” Carrie said of Dylan. “He was babbling and it helped him in so many different ways. He also just walked independently a couple months ago. For Tessa, it made her stronger. She was already smart and attentive.”

Today the twins attend therapy sessions at MedCentral Pediatric Therapy one day a week and preschool at Tri-County Preschool four days a week. They receive occupational, speech and physical therapy.

“A typical day for us includes them going to school a little after 8 and they’re picked up a little after 11,” Carrie said. “After we get them home and fed, Tessa goes down for a nap and then Dylan stays awake and I get alone time with him, which is nice. We work on walking and sitting up with them, but try to incorporate it into their play. We try to make it a fun time.”

The family takes the twins on outings by stroller and enjoy their play time together, but each day can be daunting.

“The biggest difference is the physical challenge of dressing and feeding. Tessa is in the process of being potty trained, but Dylan doesn’t want to yet,” Carrie said. “She can’t feed herself and we’re still changing diapers at age 3.

“Dylan’s not walking. If you ask him to pick up something, he doesn’t understand. It’s challenging.”

Recently, Dan and Stephanie Kreisher, of Ontario, held their third fundraiser for the family. Jeremy was on Dan’s 1994 state championship baseball team at Ontario High School.

The Kreishers and friends raised $1,400 for the Hancocks, along with providing them two iPads for Tessa and Dylan after learning the electronics would help their communication skills. The iPads were sponsored by Elite Excavating and Zara Construction.

“We have so much and are so fortunate that we wanted to help others,” Dan said. “Jeremy and Carrie are such positive people. They’re the happiest parents, just very admirable people.”

The feeling was mutual.

“I can’t say enough about Dan and Stephanie. The iPads are huge for us. We’re in the process of getting different communication devices to help with fine motor skills,” Carrie said. “They use them in school and it’s nice to be able to incorporate what they’re learning at home. Life isn’t easy, but we are very blessed.

“The best way to describe our family is that we’re taking the scenic route. We’re taking the back roads. We’ll get them there, but it just might take a little longer.”

Stem cell therapy for cerebral palsy: Sarai Nathan

“Sarai walking with assistance after stem cell therapy in panama. She could not even stand before.” – Elizabeth, Sarai’s mother

Sarai Nathan suffers from mild spastic quadriplegic cerebral palsy. She came to the Stem Cell Institute at the beginning of August 2011 when she was about 16 months old. The following is a transcription of a phone call interview with Sarai’s mother, Elisabeth. It took place on January 18, 2012 about 5 1/2 months after her stem cell procedures.

How is Sarai doing since receiving stem cell therapy five months ago?

She’s walking with very, very little support. Ever since we got the stem cell transplant, there’s been tons of progress. The major thing that I relay to people is that the stem cell treatment kind of put the cells in place to rebuild everything.

We flew right from the stem cell treatment to a place called the Napa Center and did a three-week intensive [physical therapy] program four hours per day and she was a completely different person four weeks later.

This is the most amazing, miraculous thing I have ever seen. She’s a completely different kid. Where did you go? – pediatrician

Once the stem cells migrated and rebuilt, all-of-the-sudden she was able to able to do all these things crazy quickly. It was unbelievable. She went from not being able to sit to sitting, standing cruising furniture by herself; without any assistance at all and she couldn’t even lift up her trunk prior to coming to Panama. Out of 100% being fully recovered, I would say she has had an 85% recovery since before the stem cells.

I know that the stem cells kind of laid the groundwork for that progress to be made but I definitely believe that doing the intensive right after the stem cells sealed the deal. I don’t think it was just the stem cells. I think that doing one right after the other made the progress amazing.

Did you try any other kinds of treatments before stem cells?

We tried hyperbaric [oxygen treatments] which worked but I noticed that the results regressed a little bit after a few months. It would make her spasticity better and then little by little I’d notice it start to come back 3 -5 months later. The whole thing was very expensive and time consuming though.

How did you find out about the Stem Cell Institute?

I am really active on a lot of Yahoo groups and I read about the parents who had positive results with stem cells and many had good experiences with the Stem Cell Institute. So I called them and they were really on top of getting back to me and answering all of my questions.

And my dad, who has a background in law enforcement, had it checked out as well because he said that he wouldn’t pay some crooks to inject my kid at some random place in Panama. After everything checked out, he helped me pay for it. And I am so glad that we got to do it.

What is your opinion of the doctors and medical staff at the clinic?

We tell people all the time that it was the best medical care we’ve ever received since our daughter was born. The hospitals, doctors, they were all far superior in patient care. They were prompt, professional, loving and they still check in with us all the time.

And the IV, I’ve never seen someone nail an IV that quickly. Randy Bowen [MD], who did all of her IV injections was just so good. My daughter had a huge crush on him and on the second day, actually started handing him her arm. Instead of crying when she was about to get an injection, she would look a little scared and just hand him her arm like, “Alright, just get it over with.” She was only 16 months old so it wasn’t like she could talk or anything.

What do her doctors and therapists at home think?

Well, I didn’t tell her pediatrician that we were going because I knew that he would try to talk me out of it. So I made an appointment right when we got back from the stem cells and the intensive. [at the appointment] I had her sitting on the table by herself and he walked in and said, “Oh, my God! What did you do?” I told him that we actually took her to get a stem cell transplant and he said, “This is the most amazing, miraculous thing I have ever seen. She’s a completely different kid. Where did you go?”

He was asking me about all the information for the clinic; everyone’s name and number. He also said, “I would have tried to talk you out of it so I am so glad you didn’t tell me. What happened to your child is unbelievable and it makes me want to fight and advocate for stem cells.” He’s been specializing in neuro-developmental delays for a long time and said that he would everything he could for the rest of his life to advocate for this therapy.

Now the center that did her intensive [physical therapy]…the things they said were, “I’ve never seen a child progress so quickly.” They watched her spasticity go away and they also watched her strength increase and all her therapists just kept saying, “It’s not usual for a kid to progress this quickly. She is doing exceptionally well.” All of our therapists – when we got home to Hawaii – they said the same things, “This is like a completely different child. This is unbelievable.”

And they asked me, of course, where we went.

Stem cell therapy for cerebral palsy: Tessa Hancock

The biggest thing we’ve noticed is her ability to track people and her vision. Her cognitive skills have improved. Before her stem cell treatment 7 months ago, she was like a 50 watt light bulb and she is like a 200 watts in comparison. She reacts more, holds her head up more and her hands are nice and open now, not fisted like before. Hand to mouth motion is much easier for her to do. Her range of motion, in general, is much better. She can now raise her hands over her head and she was never able to do that before.

Her therapists have seen dramatic changes. Our family has noticed changes. The neurologist has noticed changes. We are very thankful that we were able to get this treatment for her in Panama. We couldn’t imagine her not being who she is now. She is 200 times better than what she was.