Chiari Malformation Awareness Month 2022.

helenhamill's avatarat least i have a brain

Chiari Malformation Awareness is imperative.

It is – or mine is- a condition that was left unrecognised, undiagnosed and untreated for many years.

The awareness I would LOVE to be able to deliver is to the medical professionals (none of whom I want to name or shame) yet nonetheless the many doctors who by not recognising that a “substantial chiari malformation” was my condition, allowed me to degenerate for too many years.

I would like to applaud the honesty of the surgeon who when I eventually reached his care, was honest enough to tell me “i hate this condition as there is very little I can do to help cure it!”. I value him.

He did however, in the 8 hours of brain surgery remove the crippling headaches which had become an integral part of my life, and one of the reasons I had to retire from work at much…

View original post 208 more words

Unknown's avatar

Author: Kenneth

I am a person who loves the Lord, my Family & Friends. I am also play and love music.. I am registered disabled with slight Cerebral Palsy & Epilepsy. my hobbies are my pc, music & watching TV

Leave a comment