This belongs in the hands of parents who are starving for an answer for their child’s condition…

Here's How I Was Able To Gift My Son With Muscular Dystrophy A Long, Bright & Independent Future! And How You Can Too!

All without invasive treatments, drugs, expensive equipment or risky procedures!

For joining the waitlist, I’ll also give you a MONTH of MD specific recipes and shopping lists! Breakfasts, lunches, dinners and snacks all specific to replenish crucial vitamins and nutrients commonly missing in MD patients’ diet!

'Me, My Son, and Muscular Dystrophy' book cover, emphasizing a parent's guide to muscular dystrophy.

‘Me, My Son and Muscular Dystrophy’ Waitlist!

Enter your best email below to secure your copy and be notified on July 22nd, when the book goes on sale! AND receive your month of MD recipes and shopping lists!
This book and recipe guide will help you and your child to the path of independence! My son at 12 years old can run, jump and even play soccer!

And With Your Help of a Purchase on July 22nd, We Will be Able to Spread The Word Easier to More Parents!

What You Will Discover Within The Pages Of ‘Me, My Son and Muscular Dystrophy’

In this book, you will follow the story of my son and I as we discovered the 3-step process to stopping the regression of muscular dystrophy!

Through the trials, tribulations, successes and failures along the way. I will introduce you to…

Why This Book Is So Important

Nominated for “Best Inspiration” before it has officially launched, ‘Me, My Son and Muscular Dystrophy’ is not only a heartfelt story of a woman desperate to give her son the quality of life he deserves…

 

It is an actionable road map for mothers who are in the painful position of watching their son deteriorate from this dreaded disease.

 

It provides hope, courage and invaluable knowledge for parents to also accomplish the feat of gifting their child true independence.

This book belongs in the hands of parents who are starving for an answer for their child’s condition.

 

For parents who are ready to truly find out the facts and fiction about the disease their children face.

 

And for the parents who are ready to stop at nothing to give their child the future they deserve.

 

A future with a straight posture, flexibility, mobility and autonomy.

 

A future with positivity and decades of plans to look forward to.

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

If that is the future you want for your family… Having this book in your hands is the first step!

You’ll Also Get My Month Long Recipe Guide and Shopping Lists With Your Sign Up!

This exclusive recipe and shopping list is usually reserved for my personal Muscular Dystrophy clients.
It includes…

All the ingredients are specifically chosen to add crucial vitamins, nutrients, minerals that children with MD desperately need!

Valued at over $97. Yours For FREE with your sign up to the Waitlist!

What Others Have to Say...

– Mark Anastasi, author of the New York Times Bestseller The Laptop Millionaire

– Shane Wolfe, Father of Son with MD

“Get this book it’s an incredible read of a determined mother to find a cure for her child. The up and downs, the struggles. Self awareness the battles. And finally a resolution. This book gave me confirmation and affirm my journey for my cure. Great work Clementine best to you and Gabrillian.”

– Leon B Martin

“At first, I had trouble understanding Clémentine’s approach. I thought she was in denial about Gabrillan’s illness, refusing to believe that it couldn’t be cured. As a nurse, I had the opportunity to speak with doctors who confirmed that there were no real treatments, only devices to help Gaby walk.

But Clémentine didn’t want to hear any of it; she remained convinced that she could heal her son. So she began traveling the world in search of treatments and solutions. That’s how she finally found specialists who told her they could help Gaby.

Then she started training in many disciplines to best help her son. Since then, not only does Gaby not need any devices, but he has also made enormous progress and continues to do so.

This book recounts all the steps that allowed them to get there, as well as all the battles they had to fight. I truly hope that their story, their victory, will benefit other children and families and that they will see it as a real source of hope!”

– Justine Ynna, Nurse

“Several times while reading Clementine Ynna’s new book about her and her son’s fight against medical prejudices associated with Muscular Dystrophy, Clementine’s journey resonated deeply with my own experience over 40 years ago, navigating my son’s condition. Only a mother, driven by unconditional love for her sick child, truly comprehends the depth of that struggle… Thank you, Clementine. Your book is truly invaluable and deserving of attention when it is soon ready in English! Wishing you all the best for the future ❤️”

– Lone Sorensen, Founder – International Institute of Neuro Reflex Therapy

“This is a book that could help many families who have children in similar cases to Gabrillian. Clementine was brave enough not to go to allopathic doctors who advised her to do very heavy treatments which risked degrading Gabrillian’s health.

She learned a lot, she was very self-taught, she did a lot of research, and today this little boy who had little chance of having a normal life… I see him running, playing with the ball, swimming, laughing with his friends and having a normal life for a child of his age. I think the story is very touching and will allow other families to find the courage to fight against a disease that has solutions.”

I really hope you will be curious to read this book, which is really worth being shared. Whether you are concerned or not by this disease, it can help a lot of people.”

– Emilie Dédinger

Me, My Son and Muscular Dystrophy

'Me, My Son, and Muscular Dystrophy' book cover, emphasizing a parent's guide to muscular dystrophy.
Enter your best email below to secure your recipe guide, shopping lists and book copy! You’ll be notified on July 22nd, when the book goes on sale!

With Your Help of a Purchase on July 22nd, We Will be Able to Spread The Word Easier to More Parents!