Spinal Muscular Atrophy

How to Unlock Your Child Full Movement Potential

Get Updates on My New Book and Free eBook Access When It is Complete, SMA It's Not Too Late: The Secrets to Unlock You SMA Child's Full Movement Potential

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If you are like me, you have this one overarching question for your SMA child...




Your second question is... 




These were the questions I had when my first daughter received the diagnosis Spinal Muscular Atrophy (SMA), very weak type 1.

She would have been dead at two months old.

Instead we had her on life support fighting for her life and hoping this new drug, Spinraza, would help her live.

It did, BUT there was more than Spinraza.

My daughter couldn't breathe, and I had no idea how to manually teach her that.

It was like the air was crushing her.

That's when I found Michelle Turner and Movement Lesson™.

That's when I found hope; that I could do something proactively instead of waiting to see what happened.

While everyone else didn't know what the future held for my child, Michelle taught me that I could make a future of movement for my child.

The only thing I wanted was to help my daughter move; I wanted anything!

When Movement Lesson™ taught me how to manually help my daughter breathe and not be crushed by the air, I knew I could manually teach my daughter other movements I hoped she would one day accomplish.

Since then I have found other things that enhance my daughter's Movement Lesson™ experience significantly increasing her neurological health, stamina, nutrition, muscular capabilities, and so much more. 

I am including these 5 essential elements you need to have in your SMA child's daily life to unlock their full movement potential. 

Sign up for early access to excerpts of my book before it is published. 

CLICK HERE To learn 8 scoliosis exercises. These are great for children who are at risk for or currently have scoliosis.
CLICK HERE to learn 5 exercises for hand contractures or to improve hand movement. AVAILABLE SOON

Meet Erin Fulks

Mother of three children with Spinal Muscular Atrophy (SMA).

I have never felt like I had to try every therapy and alternative method out there to help my daughter achieve optimal movement in her lifetime.

I did know that I needed to find what worked. 

While what I have found requires valuable recourses and my time, it's what works.

While yes there are more traditional therapies and other methods that work, I feel I found the best combination of modalities that can support traditional therapies your are doing, or stand alone without traditional therapy.


The big kicker is you have to be willing to take the time to make what I will share with you work.

If you think you don't have time, or you would rather have someone else work on your child, then don't pursue me anymore.

If you are willing to learn new things about the body, put in the work, and incorporate effective tools into your current schedule, then I can help you.

You can ask me questions, ask for clarification, get one on one support for your child's specific movement needs. 


I Want to Work With Erin