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Heart There are many things those of us with migraine disease wish people without it understood. It is severely disabling. Symptoms can come and go. We express our desire for this understanding adville business plan and in many ways, from Twitter conversations and Facebook groups to Instagram posts.
Sometimes, it is others of us with it. The uniqueness of migraine can separate us Living with migraine is an exercise in coping with the unpredictable. Symptoms and severity can change from one attack to the next.
The disease rarely presents in exactly the same way for any two of us. At times, this uniqueness can make us feel lonely even in the midst of those whom we feel understand the most. In general, there are more similarities than differences between our experiences, which is why communities like Migraine.
It gives us hope. Occasionally, though, we still feel separate. So today I want to make a move toward lifting that veil. What I want you all to know about my migraine disease Head pain is not my most disabling symptom. This is hard to get even my neurologist to understand.
I have my pain doctor to thank for that, I know. My attacks can last for days, weeks, and even years. It is vital to my sanity and quality of life that I do more than isolate myself in a dark room.
I try to do whatever I can to distract myselfespecially when the pain is so bad no medication can touch it. This may mean watching TV, going online, or even doing something with friends. Basically, whatever I can tolerate.
At this point, I do what I can to manage my symptoms vertigo, double visionnausea, pain, etc. For me, that means taking opioids, and occasionally it means taking them more than twice per week. What do you wish the rest of us with migraine knew or understood about you and your experience with migraine disease?
Please let us know in the comments. I look forward to reading each of your responses and getting to know you all a little better.
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