PROJECT CM 1

STORIES FROM INDIVIDUALS WHO HAVE BEEN DIAGNOSED WITH AND LIVE WITH AN ADULT ONSET CHIARI MALFORMATION AND ITS RELATED SYMPTOMS. HEALING AND LIFE JOURNEYS.

This project has been in the making since 2012, beginning with my own diagnosis and the start of my chosen path of healing. In late 2012, I formed Chiari and NUCCA in order to provide information to others living with symptoms from CM 1, offering more alternatives to symptom relief and body rebalancing beyond decompression surgery, and for those that chose to have the surgery.

 

My goal with this project is to share this condition to the world in a way that is true to its nature; how we live with this every day and depending on the day, good or bad. The reason I am asking for your basic information is to continue to compile data in efforts to shed light on why symptom onset occurs. I would like to include this with your story for the publication.

You can be a part of this great endeavor and have your story published to help others understand what Chiari Malformation is and how it affects and effects us on a daily basis. Thank you!

When you're done writing your story, please email it to chiariandnucca@gmail.com. <3 

Feel free to record it with your phone as an alternative - I'll transcribe it for you.