Migraine Stories - sometimes I just break down and cry. Actually I cry a lot.

Migraine Stories - sometimes I just break down and cry. Actually I cry a lot. I'm sure my bf thinks I'm crazy lol

Migraine.com Most irritating comments about migraines.  http://migraine.com/blog/dont-call-me-that-words-that-irritate/

It is irritating to hear people say this and things like it, especially when it comes from people who know me


Now imagine this "headache" lasted over 3 years, every damn day! Worse than any migraine I've ever experienced! That's CHIARI~~~~Credit: Susan Jillian Smith

So true...wish more people understood that!

Migraine Attacks Are Disabling. I've had to try and signal other people in the house to bring me medicine if I wakeup with migraines and can't get up

I can relate...75% of the time if it's not pain it's exhaustion...only about 25% is good :(

Life doesn't stop for Chronic Illness. Life with Rheumatoid Arthritis, Auto-Immune Disease, Fibromyalgia/Chronic Illness, Pulmonary Sarcoidosis, Hyperaldosteronism.

Couldn't of said it better myself!

Raise awareness for your invisible illness and show your frustration over unsolicited medical advice with this 'my disabling chronic condition is more real than your imaginary medical expertise' gift.

Off With My Head! It Just Causes Me Pain!

In Full Flare

Do you have Cluster Headaches? You may qualify for local research studies Cluster Headaches are a rare, painful kind of severe headache.

Stigma Makes It Harder to Live with Migraine < Personally, I just don't tell people, especially clients and colleagues

Migraine is a Disease! Stigma makes it harder to live with migraines.by Teri Robert (coping with an invisible disease).