that-tall-girl
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I wanted to share this resource with everyone. Not having insurance means that I couldn't afford to see a doctor much less afford medication for my migraines.
I found this article. It has a database with doctors and specialists for free or sliding scale. They also have info on getting free or low cost medication.
https://www.axonoptics.com/migraine-medication-assistance/
Do you have any resources or tips you can share for affording migraine medications? I think there are a lot of people out there who could use it.
CrystalHarper Community Admin
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This is wonderful, @that.tall.girl! What a great resource to have and share with the rest of the community. Have you used this yourself yet?
I don't have any tips to share from experience, but I did recently see an article on ways to make acupuncture more affordable. Here's the link in case anyone is interested: https://migraine.com/blog/how-to-afford-acupuncture-for-migraines/
Looking forward to seeing some more replies from others who have any tips or tricks to share!
Kindly, Crystal (migraine.com team)
sher77 Member
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Does it ever feel to you while on this migraine journey that just as something begins to work, another thing shifts in the equation and you are back to searching for answers again? I feel that way so often. It seems like I go in 3 month bursts where if I try something new it will work for abt a 3 month slot before it shows up it’s evil side. Then we are done and it is time to call in the next bit of help… (of course, I can never change out that fast because it doesn’t work that way with tapering off meds, etc…) onward and forward! My neurologist and headache specialist says that I am not out of medication options yet!
One medication that I found beneficial has been indomethacin, taken 30 to 60 minutes before exercise, for exercise induced migraines. I got this prescription when I needed physical therapy after breaking my leg & ankle in 3 places. I was having a hard time with therapy because of migraines and this got me through. I felt like a part of therapy that I could have benefited from more was the water therapy. I walked into this large glassed in box that had a treadmill in the bottom of it. After the side door shut and sealed, water began coming up through the floor until it was about shoulder height. The physical therapist was outside the “glass box” and instructed me on different exercises and then I walked or ran on the treadmill. When you are in the water you don’t feel the impact on your joints and muscles and you are working harder than you think. This was good for my migraines, because it was a way to get moving that wasn’t painful. Unfortunately, I don’t have access to that water therapy so I can’t use it anymore. Would have been nice to test it out over a year. If anyone of you have the chance, though, I would encourage you to try it and if it takes indomethacin, then try that with it, per doctor’s orders, of course.
Wishing everyone a low pain day!
Cody Leach Community Admin
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I can also understand the complex emotions that come with finding something that works and having it fade over time. I was stuck in that cycle for many years. However, the fact that your neuro says there are still options for you is a good sign.
My migraines appear to respond very well to lifestyle changes, which I recognize is not the case for everyone. Since the beginning they were mostly triggered by sleep disruptions, excessive caffeine, the foods I ate, and scented products. I was eventually able to reduce my migraines about 95%. I went from 1 to 2 migraines per week to about once a month, maybe even once every two months. I hope with all my heart that this will happen for you too one day.
Sincerely, - Cody (Team Member)
P.S. It's also great to hear that your provider was able to find a med to help you complete physical therapy. Hydrotherapy is such a cool concept. Your town might have a community pool, or you could look for a local gym/YMCA that have open swim hours!
CommunityMember3867250 Member
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One tip I have is specifically for people who use Fiorecet for migraine and have been denied. Every Medicare supplemental plan that I have had has denied Fiorecet for migraine initially and I have had to have my PCP intervene with a letter. Luckily I have a VERY good doctor who not only understands migraine, but understands insurance denials and their system and listens to his patients. He has added TENSION HEADACHE to my diagnosis specifically to get this medication approved. It works every time and seems to be the only way to get the insurance plan to pay for it. I guess it is not approved for migraine but it is for tension headaches.
Good luck to all!
mrst53 Member
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Use your doctor