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!
‘Me, My Son and Muscular Dystrophy’ Waitlist!
And With Your Help of a Purchase, 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…
- New discoveries in the world of muscular dystrophy and the effective ways to treat it holistically
- The REAL causes of muscular dystrophy and how it can be impacted with ‘epigenetic’ components
- The detoxification process that is VITAL for children with MD
- The mindset shifts that were needed and how I went about developing a strong and positive mindset. Creating the environment for my son to feel the same way
- All of my travels to meet with numerous specialists and the shocking answers I found along the way that SIGNIFICANTLY helped Gabrillian (my son)
- The diet and nutrition secrets I discovered and the plan that proved to truly help Gabrillian. Along with a list of foods to avoid to reduce muscle loss and fatigue
- Various studies and techniques I discovered and the implementation (narrowing in on precisely what works)
- The benefits of bio resonance and how it helps with absorption of dietary supplements
- How I was able to utilize what I discovered to create the holistic and INCREDIBLY effective plan that has helped Gabrillian to not only walk, run and jump… But to play soccer at 12 years old!
- Examples of other children diagnosed with MD and their road to success
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.
If that is the future you want for your family… Having this book in your hands is the first step!
Get My Month Long Recipe Guide and Shopping Lists With Your Sign Up!
- Ingredients for each of the breakfasts, lunches, dinners and snacks for a whole month!
- Cooking and serving instructions that are really easy to follow!
- Laid out shopping lists for each week so you know EXACTLY what to get!
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! Just tell me where to send it!
What Others Have to Say...
– Mark Anastasi, author of the New York Times Bestseller The Laptop Millionaire
– Shane Wolfe, Father of Son with MD
– Lone Sorensen, Owner of the International Institute of Reflex therapy
– Peter Sage, Best Selling Author and Founder of Sage Academy
– Paul O Mahony, CEO of Rethink Academy
“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
With Your Help of a Purchase, We Will be Able to Spread The Word Easier to More Parents!