Counting My Spoons

Inspired Living with Chronic Illness

  • About Julie
    • What’s Helped Me Most
      • ToolKit
      • Vital Plan
      • Oska Pulse
    • Contact Me
    • Work With Me
    • Terms of Service
  • Warriors
  • Coping
    • Tips & Tricks
    • inspiration
  • relationships
    • Fibro and Marriage
    • friendship
  • Conditions
    • Fibromyalgia
      • Fibro Warriors
    • migraine
    • endometriosis
    • Medical Studies
    • Treatment
      • Diet and Nutrition
  • Reading List
  • Toolkit
You are here: Home / Coping / 30 Things About My Life with Migraines

30 Things About My Life with Migraines

Last Updated: June 21, 2015

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

30 Things About My Life with Migraine

My post today is part of Migraine and Headache Awareness Month. You can learn more about this 30 Things About My Life with Migraines meme at dailyheadache.com. If you blog and live with migraines or headaches of any kind be sure to share your own 30 Things answers on your blog. If you don’t blog and want to share you can do so here or over at dailyheadache.com

There are different sets of questions depending on which type of migraine/ headaches you live with. I live with both Cluster Headaches and Migraines, but I’m going to focus on the Migraine questions here.

1. My diagnosis is: Chronic Migraines and Cluster Headaches
2. My migraine attack frequency is: currently every 7-10 days. When CH hits it’s every day and sometimes multiple times per day. The longest I’ve gone between in the last couple of years is about a month.
3. I was diagnosed in: 2003 for Migraines (I think) and 2010 for Cluster Headaches
4. My comorbid conditions include: Fibromyalgia, IBS, Hypothyroid, TMJ, Endometriosis and probably a few others. I can never seem to remember all of my diagnoses at one time.
5. I take 2 medications/supplements each day for prevention and 2 medications/supplements to treat an acute attack
6. My first migraine attack was: I can’t even remember life without Migraines.
7. My most disabling migraine symptoms are: pain and sensitivity to light
8. My strangest migraine symptoms are: general weakness
9. My biggest migraine triggers are: light (I wear my sunglasses at night… sunglasses at night…). Smells are also bad for me. Processed foods.
10. I know a migraine attack is coming on when: I can’t tell I’m wearing my sunglasses inside. My neck starts getting tight from my shoulders up.
11. The most frustrating part about having a migraine attack is that it gets in the way of things I want to do.
12. During a migraine attack, I worry most about when it will end. Every time the migraines or headaches come back I worry that it’s another cluster and I’ll be stuck with them for months on end.
13. When I think about migraine between attacks, I think that I’m really thankful I don’t have one.
14. When I tell someone I have migraine, the response is usually “if I had a migraine I couldn’t stand up.”
15. When someone tells me they have migraine, I think I’m sorry that’s really got to suck. I hope it goes away soon for you.
16. When I see commercials about migraine treatments, I think “if only it were that easy.”
17. My best coping tools are my sunglasses and a Coke.
18. I find comfort in my husband.
19. I get angry when people say: I can’t really think of anything anyone has said to me that made me angry. I get frustrated when people start pulling out the laundry list of things that work for them.
20. I like it when people say: “Is there anything I can do?”
21. Something kind someone can do for me during a migraine attack is bring me a Coke. It doesn’t always work but it’s more likely to than anything other than my prescription meds.
22. The best thing(s) a doctor has ever said to me about migraine is “here’s something we can try…..”
23. The hardest thing to accept about having migraine is that they will always be there.
24. Migraine has taught me that I can push through. When you live with chronic pain of any kind eventually you learn to push through. I can’t always but most of the time I can keep going.
25. The quotation, motto, mantra, or scripture that gets me through an attack is: “this too shall pass.”
26. If I could go back to the early days of my diagnosis, I would tell myself it’s going to get worse. Then again it’s probably best that I didn’t know that.
27. The people who support me most are my husband and my mom.
28. The thing I most wish people understood about migraine is that it’s not one-size fits all, or even most. We are all different and our symptoms, triggers, and treatments vary.
29. Migraine and Headache Awareness Month is important to me because too often those of us with migraines fly under the radar. We can either hide it or we don’t show up when we have one so no one sees it.
30. One more thing I’d like to say about life with migraine is that it is survivable. It’s not fun, it sucks, but we can get through it.

3 Comments Filed Under: Coping, migraine, Symptoms

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. Katie says

    June 23, 2015 at 11:48 am

    I deal with migraines and fibromyalgia along with mood disorder and anxiety. I know they are all linked somehow. I am fortunate to live in Colorado as the best treatment for me is about 20mg THC, and a pepsi made with sugar not corn syrup. I think it is interesting how many of us need a cola to get through! I have tried Imitrix, and other meds, but the best for me is the cola/mmj combo. Hope you get more relief soon, there is no magic bullet.

    Reply
  2. Nancy says

    June 22, 2015 at 6:37 am

    I just read your post. I had severe Migraines before menopause. It controlled my life.
    When I read your post it broke my heart that another Migraine sister is going through Migraine disease in that severity. I am so sorry… There is a light at the end of the tunnel. You may email me if you like. Nancy

    Reply

Leave a Reply Cancel reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

Common Tags

abdominal pain acceptance alternative therapies anxiety asking for help book review books brain fog cbd oil chronic fatigue chronic illness chronic pain communication dairy-free dealing with doctors decreasing pain decreasing stress depression diagnosis diet doctors documentary family feeling better flares food sensitivities gifts health holidays ibs interviews mental health oska pacing pain relief product review review self-compassion sensitivities sleep sleep aids stress sunday inspiration support travel

Copyright

All content copyright CountingMySpoons Any content reblogged from this site must adhere to the terms of © Copyright and TOS
That page states in part: "A brief excerpt of content that does not exceed 75 words may be quoted as long as a link is provided back to the source page on this blog and authorship is properly attributed."

Proudly Hosted By:

Wordpress Hosting Done Right

Proud To Be Included

 

Chronic Illness Bloggers
 

Privacy Policy

Counting My Spoons respects your privacy. Your information will never be provided to any third party unless you provide explicit permission to do so (something I'm not likely to ever ask you to do).

Read full privacy policy

Content Copyright © 2025 - Webz Plus Inc