Hi,
My name is Kari Bjorn and I've had CH for the past 11 years. These 11 years started out with a lot of panicking and fear but I'm very grateful that I was diagnosed within 2 years and have been able to manage it somewhat since then. I was prescribed sumatriptan only for the first 3-4 years that helped me 70% of the time and in 2012 I saw a neurologist that put me on 80mg's of verapamil that took the pain away for the past 2 1/2 years, until last fall when the beast started coming again. This past cycle was terrible as I had just gone back to college to study photography. Before the cycles were very predictable, I could pretty much take a tablet of sumatriptan at certain time and all I would get were shadows.
This cycle has been hell to say the least, it started august 28th 2014 and I'm not sure if it's still going. I got the pain on the left side this cycle and on november 20th as I was getting ready for the headaches to slowly get less severe and fade out I started a new cycle in the right side of my head and with less and less predictability. By December 15th I had taken so much sumatriptan (and they had stopped working at that time) my doctor told me I was "temporarily immune" (not exact words).
I came to this site which I've visited through the years but never subscribed to look up some alternative solutions. I was put on prednisone, first 60mg for 3 days and then gradually less dosage until today when I swallowed the last 5mg tablet.
I also started taking Omega3 fish oil, huge dose of vitamin D and Lısi (another fish oil product from my home country, Iceland)
Just 24 hours after taking the prednisone the pain was gone except for maybe 3-4 shadows in the past 3 weeks. I've been worried that I might have gone from episodic to chronic since this switch from the pain being on the left to the right has never happened before and the cycle was unbelievably unpredictable, painful and long, my previous cycles have usually started around September 15th, reached a peak around october 20th when I would get them 6 times a day and would start to fade out around November 15th and then be gone around December 10th.
It would be nice to know if there's anyone who knows the symptoms of switching from episodic to chronic. I don't know what I'll do if this happens to be chronic, to go from something that I could manage into possibly getting CH everyday for years to come. I'm very scared of that.
Thank you for reading and please check out my other post
I'm studying photography at Parsons in NYC and I'm starting a project around CH. Please contact me if you're interested.
Kari Bjorn Thorleifsson
KariBjorn wrote on Jan 8th, 2015 at 8:04pm:Hi,
My name is Kari Bjorn and I've had with cluster headaches for the past 11 years or almost half my life, I'm 27 now. I'm currently studying photography at Parsons in NYC, previously I was/is a chef and worked in kitchens back home in Reykjavik, Iceland, NYC and London, UK.
I want to start a project around Cluster headaches and its sufferers, this is something I've been thinking of for the past few years but never really started except for a few self portraits. I'm not really familiar how much CH is "known" in the US but back home none really knows CH and I've always had to explain in detail, to new friends, bosses, coworkers etc.
My goal is to tell the story of the cluster head, as broad as it is at this moment I see this as a project I will work on for a few years and will hopefully develop along the way.
I'm looking for people in New York to get in contact with that either have CH and/or know someone close to them that has CH.
Please contact me at thork317@newschool.edu
Kari Bjorn Thorleifsson