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Just got my annual migraine

Hi everyone- just joined after looking up symptoms because I’ve just had my roughly annual migraine. I say annual, they’re more once every 12-18 months I think, quite infrequent anyway. But when they do occur everything is halted. Work, time with my partner, social events all have to be called off so I can lie in a darkened room.

I first experienced it in my teenage years (I’m now 42), one day I had to go home eatly from school and go straight to sleep late one morning, which lasted right through until that night. I’ve had them on several other occasions, a few of which stick out in my memory. I remember one about a decade ago when in work where I got the nausea and aura, but not the headache. On that occasion I completely forgot a colleagues name and couldn’t recover it in my mind, which felt quite scary.

I did go several years since that experience without a migraine, but they seemed to have returned the past few years.

Does anyone else feel like a bit of a fraud when telling people about your migraine. Today I was getting ready go to into work as I was unsure if my migraine was that bad, although I had experienced the aura earlier this morning and also had a stomach upset (which I thought was a coincidence but now realise could be linked), and had a headache. What sealed the deal was when my partner was speaking to me, and concentrating on what she was saying made my headache worse. I called in sick, but I can’t help shake off the feeling that both my partner and my boss don’t believe me. This is compounded when having been in a dark room for an hour or so, I start to feel better.

I know with the lower frequency and (I think) less severe symptoms I’m not a particularly extreme case, but these factors actually make doubt myself somewhat. I have absolutely no idea what causes them, and it feels too infrequent to spot any patterns. The only thing that might be consistent is that they seem to happen around this time of year, ie spring or summer. I live in Scotland so it’s not a particularly warm or cold place, very few climate extremes here which would suggest anything.

Wondered if anyone else is in the same boat? I did find the explanations on the website very reassuring, even down to the ‘washed out’ feeling afterwards.

  1. I am on Ajovy injections once a month. Last month they were late sending it and unfortunately, i had to leave before it got here so it was delayed by 4 days. I ended up with a massive migraine..the aura, vomiting, etc.. I have been on this for almost two years and have had at least 8 migraines, but better then the amount I used to get. If I am not on time due to shipping time...I am the one that suffers not the shipping company. However, I know It cannot be helped due to inclement weather at times. My ajovy has been making the injection spot itchy. Then a small rash occurs for 3 days after. My doctor says if it is something that can be tolerated then don't complain. He says take an allergy pill 30 min before injecting. It helps but it is still itchy...so I use a topical on it till the itching ceases. I found it strange that this started after using it for 19 months without any type of reaction.


    1. Thank you for reaching out and sharing your experience with us. Ajovy sounds like it' s been very successful for you, except when there's a delay. It's awful to be at the mercy of the shipping company.
      While Ajovy isn't a cure for migraine (we don't have one yet) it can go a long way in helping reduce attacks! I'm so glad you are experiencing relief.
      Ajovy can cause this sort of reaction, but you're right, it is interesting it happed 19 months after you started it. Hopefully others will be along shortly to share their experiences with you on this.
      Wishing you a low pain day, Nancy Harris Bonk Patient Leader/Moderator Migraine.com Team

  2. Hi
    Thank you for joining our community and sharing your experience with us. Whether you have infrequent or frequent attacks - all are welcome here!

    Here's the deal - migraine is a neurological disease that falls on a spectrum from mild to severely debilitating. One or two debilitating attacks a year can wreck havoc on our lives and doesn't make your experience any less valid than those who have frequent attacks. Please know we're here for you!
    How long did your attack last? I hope you are feeling better and look forward to hearing from you.

    PS My sister just go back from Scotland and loved it.

    Nancy Harris Bonk, Patient Leader/Moderator Migraine.com Team

    1. HI - Thanks for sharing some of your journey with us. I found your story interesting- wondered if there's anything you can attribute the annual migraine to? Change in the season? Work stress? And yes, because migraine is an invisible condition, many of us can struggle with helping others understand or believe that we are truly experiencing a complex neurological condition since they can't see it. It's a real challenge! Warmly- Holly -migraine.com team

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