Daily Migraines - How do we function?

Posted by heysie @heysie, Jul 26, 2025

Medications, PT, sound baths, massages, the ice gel cap helmet thing, occasional fevers. The vice grips tightening on the temples. The thunder claps through the top of the skull. The bludgeoned feeling at the back of the head. The nausea - oh god the nausea. And the advice is to eat well and go for a walk and don’t overdo do it on the ibuprofen, which might as well be tic tacs at this point!

If any of this rings a bell or resonates, please join me in this conversation on how to survive and function with these symptoms and headaches as part of our lives. Granted, I’ve had two sinus surgeries for sphenoid sinusitis in the last year and an infection for meningitis, but the migraines remain and continue to develop the cruelest symptoms.

I need help understanding this and knowing I’m not alone. All I’ve got in my arsenal is rizatriptan and Tylenol #4 oh and topamax.

How about you?

Interested in more discussions like this? Go to the Headache & Migraine Support Group.

Profile picture for jnhuver @jnhuver

Okay, I am at a loss of what to do, and this seems to be my last straw as I am reaching out for help from fellow migrainers. I turned 50 a year ago and the intense pain of headaches, not stopping tasting for hours or days with no end in sight. I had a MRI done, nothing drastic except small vessel disease (PCP wasn't worried, unlike me). I went to a neurologist out of network who prescribed Aimovig, migraine from hell ten times worse then I have ever experienced and all I got was to take it next month as this is rare and will go away. Needless to say, I stopped it because the pain was to great. I am on Topamax nightly but I take it for other issues as well, doesn't help with migraines. Then when I did get into a neurologist a year later, I was prescribed Amtripyline doesn't work, and then I was prescribed Emgality and the day after it gave me adverse reactions, (the neurologists didn't look at my illnesses/conditions to know that I have Chronic Hives, so therefore this new drug, is capable of bringing out my hives), it also gave me a fever and I just got told to continue with it for another 3 to 6 months. Frankly all I want is the root cause, why I have them, what causes them, because I don't have triggers. And they are in my frontal and temples, no nausea, what you guys are saying you have. I have no idea when they come, they just there, I can go to bed with them, and wake up with them, who knows what happens at night while I am sleeping. Its frustrating and I am so ready to fire my neurologist and find someone willing to help with root causes and stop giving me meds that affect my conditions and give me allergic reactions but tell me that I am lieing... Any sugguestions

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@jnhuver Have you ever talked to a neurologist about taking Botox injections? You get them every three months and they control the migraines better than any other medication they have had me take, and I have had no side effects other occasional mild headaches. I’ve been getting Botox for 25 years now, and they have literally saved my life. I had intractable severe migraines for over a year straight. So many meds tried and failed with some not so pleasant side effects. Even tried cervical traction with no relief. Finally my PCP referred me to a fourth neurologist - who examined me and told me if I could handle a series of injections to my upper back and neck, then I could leave the office with no headache. I didn’t believe him, but was willing to try anything. The diagnosis was cervical dystonia, which is progressive if untreated - symptoms include severe headaches which are constant, balance issues, and brain fog, and muscle spasms in the back and neck. He only gave me a block to the nerves affected at first, and the results were immediate and unbelievable. The block only lasted for several days, but when given the Botox the relief lasted almost three months. It was incredible to wake up with no headache or a stiff neck and upper back and to feel that good all day. I’ve been on Botox for 25 years now, and have very few breakthrough headaches. Even when I do get a headache, it is never of the intensity that migraines would cause. At the end of the Botox cycle- 3 months- I may have 7 to 10 days of migraines as it’s wearing off, but to have most of those months headache free - priceless!

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