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Great idea! I made a spreadsheet that tracked how many per day, what time they started and what meds I used to treat them. Doc loved the information, but felt bad that I was having on average 3 to 5 days a week with attacks. The only way I was able to work was that 95% of my attacks started at 3:00pm with a migraine and within 1 to 1 1/2 hours the cluster events would start and by then I would be home. To have 1 week shy of 6 months pain free thanks to Clusterbusters is a life saving experience.

One thing I'll add on the O2 is follow every thing they describe on the links here. It did not work for me until I did. Also don't be afraid to go to "welding" oxygen route. I have for some time now and the only difference I have found is it's cheaper for me and I don't fight with my insurance anymore. And share these posts with your wife and let her know we all care and are in her corner.