Rehabilitation Program for mothers with Muscular Dystrophy children

I help mothers with MD children who lost muscle strength and vitality to see their children to increase strength , grow muscles and live a healthier and autonomous life

Through My Muscular Dystrophy No More 4X program

Portrait of Clementine Ynna, founder of 'Me, My Son, and Muscular Dystrophy,' smiling warmly, wither her young son, embodying hope and resilience.

About me

‘Me, My Son and Muscular Dystrophy’

This is not only the personal story of how we overcame muscular dystrophy, but a guide for you to do the same!

‘Me, My Son and Muscular Dystrophy’

This is not only the personal story of how we overcame muscular dystrophy, but a guide for you to do the same!

I am Clementine Ynna and I am a Neuro Reflex Rehabilitation specialist.

I help mothers with Muscular Dystrophy children

who lost muscle strength and vitality to see their children to increase strength, grow muscles and live a healthier and autonomous life!

Mothers who have tried many different things and are disappointed about traditional medical care, and are tired of waiting for a cure!

What distinguishes my services from other doctors, naturopath, physiotherapists, is that I am myself a mother with MD child who I successfully rehabilitated. I have personal experience in my own life.

What else separates me from is that I have more than 17 years of experience in helping people with severe conditions. I have specialized for MD and I have used different techniques for that condition.

 

Thanks to that, mothers can see their children moving again, growing their muscles, have more energy and live a happy healthy life.

Muscular Dystrophy children walking
Mother_child

I am from France. I am a mother of a beautiful 9 year old boy born with Muscular Dystrophy.

 

After learning the terrible news of my son’s condition, I was devastated but didn’t give up on finding ways to improve the quality of his life. And with the help of the best healers, physicians, specialists I went in search for solutions and against all odds and certainly against the western medical system.

 

I eventually graduated with a Master in Natural Eastern therapies such as Acupressure, Ayurveda and Reflexology from universities in France, a degree in Herbalism, and it’s naturally that I undertake the exploration of ancient traditions to find out the Real Truth about Muscular Dystrophy.

 

Those intensive researches led me to unique discoveries and techniques from the latest advances in Neuroscience, Quantum physics and Epigenetics.

 

Today my son can walk, jump and run!

 

I have been invited for many lectures, interviews to explain what I have done to reverse the “genetic dis- order” of my son and talk about my project for the first family Retreat in Europe for Muscular Dystrophy children and adults.

 

 

Today, I am a neuro reflex specialist and I am training families around the world to empower parents to heal their own children with natural and non-invasive methods.

 

 

I guide parents with Muscular Dystrophy children who lost muscle strength , vitality and parents who feel hopeless and I help them to see their children to increase strength , develop muscles and live a healthier and autonomous life!

 

Would you like me to guide you personally and see your child to strengthen muscles, improve balance and increase vitality?

Perhaps, you are also a mother with Muscular Dystrophy child...

…and feel sometimes hopeless from the situation? Maybe you experience sometimes doubts about what to do or you often feel alone without proper guidance?

 

We can discuss about your special needs and challenges with your child and work together on a plan during an introductory session. This is a 30-min session (completely free for you) where I get to know your situation and then help you create your program and discuss with you the possible solutions.

My story

I still remember how Gabrillian, my son used to fall down , he had no balance , it was like he was walking around with his arms always holding onto the table or the wall.

 

It was my first child and I had no idea so I didn’t worry. At 2 years old he was still not walking , doctors talked about “muscle weakness”…

 

After many visits , tests I finally learn that my son has a rare form of Muscular Dystrophy , that he might never walk properly, even get complication with his heart, his lungs and that there was no cure .…

 

I was devastated

Portrait of Clementine Ynna, founder of 'Me, My Son, and Muscular Dystrophy,' smiling warmly, with her son, embodying hope and resilience.

The first lesson that I learned during this journey , was “to take the risk to believe no matter what !”

 

One day while working on my computer I came across this quote :“ when we are no longer able to change a situation, we are challenged to change ourselves…”

 

From that day, I made a decision: I will work on myself!

 

I was committed and slowly , slowly things started to change …

And one day , my friend Mark who is a coach and a writer called me and told me : Clementine, I’m writing a book about health and there are solutions out there! Are you ready to try?”

 

One part of me was saying don’t be naive, its impossible ! There are no cure!

 

But the other part of me, this part I have been training for months started to say “You makes things possible …you can do it…go for it!

This open mind led me to many opportunities …

 

 

 

I’ve also learned a unique therapy called Neuro Reflex therapy while searching of solutions for my son’s learning abilities and behaviour problems.

 

Every day, the teacher would complain about my son: “Gabrillian can’t sit, he doesn’t listen , he’s disturbing the class, please talk to him…”

And of course, I have been talking to him many times, I punished him, I even brought him to psychologist but nothing seems to work …

Mother_child

I was feeling hopeless , I didn’t know what to do !


And I thought it must be solution for this too…And I found out about Neuro reflex Therapy.

I was doing therapies to Gabrillian 3-4 times a week …


And one month after , the teacher of Gabrillian told me : “ I want to talk with you” and I thought “ OMG , what’s happen again !!”


And she told me “ I just wanted to tell you that Gabrillian has made so much efforts , he can now sit , he listens and he is really trying to follow instructions..”

I was so happy.


Slowly slowly I also noticed that he stopped complain about pain in his writs while writing or pain in his legs while walking…


After seeing those results and watching a youtube video showing a rescued family in Oman with 3 disabled children, I decided that I had to go there to research further. There I discovered a unique system of family training for disabled children. I then decided to bring this system to Cyprus and to create the Only one Family Retreat for Muscular illnesses in Europe.


At my return, I started to work on Gabrillian 4 times a week with a new protocol to stimulate more of his motor function and his muscle’s strength and to my huge surprise after a month of stimulation, Gabrillian started to jump for the first time.


I then embarked on a journey to became an expert in Neuro Reflex Rehabilitation therapy to keep on improving the abilities of my son and share with others my discoveries and knowledge to help empower them and their families to stimulate the recovery of their own children.


One of the latest improvements of Gabrillian happened during the COVID lockdown. For a whole month he wasn’t able to go to his habitual physiotherapy twice a week. And we noticed that his spine started to go more to the side accentuating his scoliosis and making his belly even more prominent.


I decided at this point to start one of the therapies on him that I learned, this would help to re-align the spine and correct his posture. After only one session the results were incredible, his whole spine became straighter, his body posture was different his prominent belly became far less prominent. After 3 months, we finally went to the orthopaedist who confirmed that Gabrilian is now free of scoliosis.


This was a great progress for us as the physiotherapist were now able to work more on his trunk and his balance.

Gabrillian is now a happy boy, enjoying playing football at school and participating in other activities.

Would you like me to guide you personally and see your child to strengthen muscles, improve balance and increase vitality?

Perhaps, you are also a mother with Muscular Dystrophy child...

…and feel sometimes hopeless from the situation? Maybe you experience sometimes doubts about what to do or you often feel alone without proper guidance?

 

We can discuss about your special needs and challenges with your child and work together on a plan during an introductory session. This is a 30-min session (completely free for you) where I get to know your situation and then help you create your program and discuss with you the possible solutions.