Jenney’s story

I was diagnosed with migraines and cluster headaches at age 14, when I woke up screaming and thinking my head exploded. My mother, who also suffers from migraines, asked me pointed questions and because my brother was fighting an illness, searched out a doctor that did numerous tests and came to this diagnosis.

I am now 42, and my migraines are changing, becoming harder to abort with most lasting 4-6 days, my medicine for aborting was recently changed to a higher dose, and even with lifestyle changes I could make, I still get 8-12 a month.

My job does nothing to help with this (I am in customer service) because my boss does not believe these are nothing more but simple headaches so I cannot call in without problems. I have applied for disability, but I am doubtful I will win, at least at first. These headaches impact my life to the point I am not as social as before, but I still plow on and sometimes force myself to join in so I don’t disappoint family and friends.

I guess as a long time sufferer that has “heard, seen and done it all” to get a handle on these, my depression as also intensified. I am glad that there is a site such as this to help me remember I am not alone in this.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Migraine.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

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