Hi, was a member before and someone royally Pissed me off at the time so I left.(please dont ask who, its not relavant) Alot has changed with my health.
I am a chronic cluster head 8 years 4 months, minimum 9030+ attacks, and 16,000+ hours of attacks.(nothing in comparrison to some of you) 1 attack is too much.
I have had 4 brain surgeries.
ONS and DBS.
I have a blog I write on clusterheadaches and my life
and youtube videos and twitter


I am canadian and on disability because of CCH.
I am a member on ClusterBusters(I do not bust)
I am a member on OUCH UK.
Im a strong vocal advocate for Cluster Headaches and doing best I can spreading awareness globally. And helping those who suffer by inspiring them to think outside the box.
Wishing all fellow Cluster Heads PFDs, and their families who live with htme are heros in my humble opinion.
Any questions?

Welcome home CHS.  Howz the head now after all the surgery?

Take care,

V/R, Batch