Headache and Migraine Group: Let’s connect
Welcome to the Headache & Migraine support group on Mayo Clinic Connect.
If you or someone you care about has headaches or migraines, this is a great place to talk with others with similar experiences. It’s a welcoming forum to learn from each other and share stories about challenges, coping strategies, setbacks and what helps.
Take these steps to participate in the group:
- Follow the group.
- Browse topics.
- Use the group search to find answers to your questions.
- Introduce yourself.
Pull up a chair and chat. Why not start by introducing yourself? What is your experience, or your loved one’s experience, living with headache or migraine (i.e., what type, how long since diagnosis, how it’s managed)? Have a question, tip or story to share?
Interested in more discussions like this? Go to the Headache & Migraine Support Group.
I suffered migraine from 20 years old until past 60 years old. Trying many meds until finally Imitrex was developed along the way and it helped. Mine came on with an aura in the right temple and what looked like broken glass. They usually lasted 3 to 4 days with vomiting. I'm now 80. Two years ago I was diagnosed with Ramsey Hunt Syndrome which has caused severe headaches, not as bad as migraine but BAD. Dr. prescribed Topiramate 100 mg at bed time and it has worked. I sincerely believe nothing has ever hurt as bad as the migraines I had when I was young, they were truly debilitating. When I hear of someone having a true migraine my heart aches for them. I wish all of you are able to get help.
I wake up with pain, vomiting, light sensitivity. My headache is fully engaged by the time I open my eyes.
Is this typical? I did not suffer from migraine until I developed dysautonomia.
Imitrex worked for years, but I have recently started experiencing abnormal heart rhythm when I take it.
I have a platelet disorder so many pain relievers are not recommended. I have no idea where to go from here.
I’ve had migraines for most of my life. I’m 61 now. Used Maxalt successfully but recently the headaches became more frequent and I had to take more Maxalt than my doctor was comfortable with. I’ve had other treatments over the years including Botox injections that did nothing. Finally after a new evaluation by Neurology (specializing in migraine) I started Emgality, a once a month self injection. Absolutely life changing. I have not had one migraine since September. Mild headache occasionally but no big deal. Truly incredible.
I am 62 years old and have suffered from migraines for 20 years. I used to get them 4 days/week and have tried every medication, Botox and other injections currently on the market as well as some non traditional ideas. Rizatriptan (Maxalt) did help a lot in stopping my migraines when they occurred. However, it did not reduce the amount migraines and at times I had rebound headaches. I now get Vyepti infusions quarterly and only experience one migraine/month. I still use the Rizatriptan as a rescue drug when I do have a migraine. This has been life changing for me.
Did Botox help you at all? I am getting Botox on the 19th. Not hopeful as it did not work 8 years ago.
I did 8 rounds and it helped 4 of those times. It greatly reduced the severity and number of migraines for the times it worked. I experienced minimal impact the other 4 times. Good luck with your injections. I hope it works well for you.
I am more worried about my eyes and how close it will be. I have macular degen & glaucoma. The neurologist has agreed to keep it directly away from my eyes.