Hi there, no I don’t generally come on this board any longer. In the email that’s associated with it. I don’t go to so often either. But I did see your message and I thought I would respond to you. No, I have not found any relief symptoms of become more frequent And more varied. I’m learning to live with them better although they can still be pretty debilitating. But actually just a week or so ago I stumbled across something else quite by accident that I am looking into. It’s called functional neurological disorder.FND. There are things about that that kind of steer me in that direction now that more relate to me as far as what might be causing it. I have not had any sort of official diagnosis by anyone. They’re all afraid to even call it migrainous. I’m on no medication’s. I won’t do that because I don’t even know what I have And neither do they. What else is interesting? Is just this week. I had an annual physical. For the most part, those are a waste of time especially when you’re dealing with all the symptoms that I am and apparently you are as well. But my primary care Wondered if I would be willing to go beyond my local area for potential help. I had said I’ve run out anything that’s available in the Grand Rapids area. He suggesting the MAYO clinics. I told him I had tried that back in December 2021. He said he would write a letter. I’m not sure I’m gonna go that route just yet there’s a lot to consider. So the short answer to your question, no, I have not found relief. If you decide to respond back to this, I will try to keep an eye on my email I wish you the best. I won’t be going back through this memo to correct errors so if there’s anything that’s confusing, I apologize for that.