Disclaimer: Nothing on this blog is intended as medical or legal advice.

What I write on this site is my own, and if it is someone else's, I take special care to attribute it to the original author. So, please don't use any of my material without proper attribution or permission. Thanks.

Monday, June 29, 2015

30 Things About My Life With Migraine

Kerrie Smyres started a "30 Things About Your Life With Migraine" meme to encourage others to share their experience with migraine. Migraine and Headache Awareness month is a great time to share, so here we go.
  1. My diagnosis is: chronic migraine with and without aura.
  2. My migraine attack frequency is: I have some level of head pain daily. 
  3. I was diagnosed in: 2002 with migraine, becoming chronic in 2008.
  4. My comorbid conditions include: depression, anxiety, fibromyalgia.
  5. I take one medications/supplements each day for prevention and four medications/supplements to treat an acute attack.
  6. My first migraine attack was: I'm not sure. The more I learn about migraines, the more I believe that I've dealt with them since childhood.
  7. My most disabling migraine symptoms are: pain, fatigue, cognitive difficulties, aphasia, sensory sensitivities (to light, sound, smell, taste, touch).
  8. My strangest migraine symptoms are: olfactory hallucinations.
  9. My biggest migraine triggers are: weather changes, lights (especially bright and/or flashing), odors / fragrance / smoke, foods / food additives (bananas, artificial sweeteners, nitrates / nitrites, MSG).
  10. I know a migraine attack is coming on when: I have difficulty controlling body temperature and moods, my ears feel hot and achy, increasing visual disturbance, certain cravings, aphasia, inability to focus.
  11. The most frustrating part about having a migraine attack is: being suddenly unable to function well, and not knowing when one will hit or how long it will last.
  12. During a migraine attack, I worry most about: how well my migraine treatment will work, and how long I'm going to be out of commission.
  13. When I think about migraine between attacks, I think: please don't worsen today.
  14. When I tell someone I have migraine, the response is usually: kind, but often indicative of the lack of public awareness of what migraine truly is.
  15. When someone tells me they have migraine, I think: that migraine is so much more common than most people think. I also think about how I might be able to help them cope with migraine.
  16. When I see commercials about migraine treatments, I think: how far we have to go (and how important it really is that we do so, every chance we get) to inform and raise awareness of migraine and the potentially debilitating affects this disease. 
  17. My best coping tools are: my faith, distraction (often involving Netflix).
  18. I find comfort in: my husband, my dog, my house, my support system (family and friends, both in person and online).
  19. I get angry when people say: "It's just a headache," which is sometimes followed by,"Just take a pill and keep going / move on" and/or "It can't be that bad."
  20. I like it when people say: a sincere, "You're in my thoughts and prayers."
  21. Something kind someone can do for me during a migraine attack is: allow me to escape to a dark, quiet place. Ask if I need anything (water, food, blanket, pillow, to be alone, etc) to help make me more comfortable. Be patient with me, as it can be difficult for me to think, speak, and move.
  22. The best thing(s) a doctor has ever said to me about migraine is: "I won't give up on you."
  23. The hardest thing to accept about having migraine is: that it is unpredictable.
  24. Migraine has taught me: to recognize the strength that I DO have. It is teaching me to have more patience, and to trust God more.
  25. The quotation, motto, mantra, or scripture that gets me through an attack is: "Be still, and know that I am God" (Psalm 46:10).
  26. If I could go back to the early days of my diagnosis, I would tell myself: to prepare for things to be beyond difficult, but to never give up hope.
  27. The people who support me most are: my husband, my support system (family and friends, both in person and online).
  28. The thing I most wish people understood about migraine is: it's a genetic neurological disease for which, there is currently NO cure.
  29. Migraine and Headache Awareness Month is important to me because: I feel that we need to speak up/out to raise awareness, increase research, and help correct misinformation.
  30. One more thing I’d like to say about life with migraine is: that it's hard, but find yourself a support system and be your own best advocate to getting the care and treatment you need to live the best life possible.

2 comments:

  1. Thanks for being so open, honest and for educating others. As a chronic migraine sufferer for the past 18 years, you covered just about everything much better than I could. It's by the grace of God I get through each day. So glad He lead me to this.

    ReplyDelete
  2. Thanks for educating others about migraine and being so open and honest. I have had chronic migraine for 18 years and could never have said this so beautifully. The Lord has given you this precious writing gift and we appreciate your willingness to share. May He bless you and praying for your healing.

    ReplyDelete