Patheticfern

I'm in the works of getting officially diagnosed by a primary physician, hoping to be able to get on O2 and/or some sort of medication. The soonest that they can see me is October 11th at the moment. Any tips and tricks to survive till I can see them?

After 2 years cluster free I am back. I had an attack today. Still shaking. I will take any advice or information that you guys have. Or share what has helped you Meds? Anyone have referrals to doctors in Utah preferably Salt Lake area?

I'm not sure the percentage. I take 1/2 mL 2x a day. Then I smoke CBD or take another dose if I feel an onset of a cluster. This is the CBD I use. https://cbdamericanshaman.com/water-soluble-full-spectrum-hemp-oil-30ml

I saw that too. That would be amazing to go to!

My cluster season is set to start soon. Not excited get a feeling of dread just thinking about it. I want to figure out my options before they hit so I'm prepared. What do you guys do? I want to know what helps and works for you guys. I know my options are: oxygen, busting, or living through it. Last year I couldn't try busting because I was pregnant. I did take a daily dose of CBD and that seemed to help. I'm so happy this forum exists so we can all be there for each other and know we're not alone. Also anyone from UT that knows a good DR to go to?

I'm hearing that CBD is either a hit or a miss with cluster headaches. If it has worked for you let me know what you do. I thought I would give it a try. If it doesn't help my clusters at least it has other benefits. I have water soluble drops that I'll take 2x a day and a vape pen that I'll try for onset of a headache