My Nonprofit Reviews

My fourth child, Parker, has been on the protocol since he was 14 months old. The changes are noticeable by all he meets. He is an active, engaged, inquisitive, verbal 2 yr old thanks to the protocol. The foundation gives accurate, medical information that can be easily shared with the physicians. All of the recommendations are linked to medical documents/articles explaining the science behind each piece. All of my son's physicians were in support of the protocol and they could not believe they had not heard of this progress sooner. Parker is different than other children his age with DS, there is not one parent or new physician that meets him that does not ask me, "what are you doing differently?" I'm excited to be able to share our successes and point them to new hope for their children. When we first learned of our son's dx we were told there was "nothing we could do," and we would not "know what he could do until he was older." We learned that simply isn't the case and we feel blessed to have been introduced to CMF at such an early age. Now, our goal is to help other parents know that there are ways to help improve cognitive function and prevent decline!

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