After 7 years with episodic clusters and nothing more than a prescription for Imitrex, I finally have some hope. Up 'till this past Friday evening, I had never met another Cluster sufferer, and now I feel like a member of one of the most supportive families that I could imagine.
Just like the diversity of our cluster community(and that of Portland itself), I'm so struck by the range of experience that the conference provided. On one hand, there's the wealth of information by the extremely knowledgeable doctors that presented. Previously, I hardly understood what was biologically going on with me, but now I feel like I just completed a medical school course on the subject. And on the other hand, the outpouring of emotion... compassion, sympathy, optimism, brother/sisterhood is still choking me up as I write this. There just aren't words to describe how much this has meant to me.
It's taken me about 6 weeks to finally type up this first post. Partially because I was in the throws of my annual July episode, but also because of negative experiences on other forums. Let me say that if anyone is apprehensive about speaking about what they're going through like I was..... Don't Be! The folks that make up this community are open minded, intelligent and compassionate people that welcomed this newbie with arms open. And if your style is a little more on the private or 1-on-1 side, send a p.m. or come to the next conference like I did.Â
I'd like to thank everyone again personally by name right now, but that'll take quite a while and ya'll know who you are. But seriously....THANK YOU for the truly life changing experience!!!
-Daniel