Archive for June 2022
I’m Just A Mom — And My Child Lives with Migraine
Being a mom is one of the most fantastic and challenging jobs in the world. We must be quick on our feet, know how to heal a boo-boo with a kiss, create a meal everyone enjoys, keep the house tidy and about a million little tasks in between. I never received the “How to be…
Read MoreMigraine Action Plan: Begins with Access to Care
Are you satisfied with your migraine treatment plan? Do you have barriers to care? As a diverse population with diverse types of migraine, we each require personalized migraine action plans. To create a migraine action plan that you are satisfied with and is successful, you need to have access to any and all resources. Care…
Read MoreShades for Migraine Community Leader: Finding My Calling
In 2017, I learned about the Shades for Migraine campaign. I immediately fell in love with it. When I learned about the Shades for Migraine Community Leader Program, I had to be a part of it. Since 2020, my goal is to get as many people involved as possible, hoping to get someone from all…
Read MoreHow Implicit Bias and Medical Gaslighting Hurt BIPOC
Being a Black woman living with chronic daily migraine for more than 14 years has exhausted me. Having to traverse a system that is set up to fail me repeatedly withers me down to wanting to give up. The number of times I had to fight for the care I deserve is disheartening and sad.…
Read MoreFighting for Access & Advocating with Dr. G
Dr. Melissa Geraghty, Psy. D, is a fierce advocate. Looking at her CV, you are struck by her vast experience working on behalf of others. In addition to her many years as a successful Licensed Clinical Health Psychologist, she is a board member for the Coalition for Headache and Migraine Patients (CHAMP), a past board…
Read MoreMigraine Advocacy Makes Me a Better Mom
Advocacy is empowerment. Migraine advocacy makes me a better mom in ways I hadn’t expected. I have more: education; connections; fundraising experience; and involvement raising awareness for the migraine and headache disorders community. When I first started my advocacy journey, I knew it would benefit my relationship with migraine, but what I didn’t know is…
Read MoreMultiple Chronic Pain Conditions: When Chronic Migraine Takes A Backseat
Multiple Chronic Pain Conditions: A Metaphorical Tale Imagine rushing out to your car, and to your dismay, you notice a flat tire. With no spare tire, you realize you’re going to be late for work, again. You have no choice but to call AAA to come replace the tire. After you anxiously pace the block…
Read MoreHigh School With Migraine: 8 Ways I’m Surviving
Being a teen and struggling with migraine is very hard. I’m 17 years old and was diagnosed with migraine at age 10; but I have lived with migraine my whole life. I have dealt with difficult teachers and administrators; stigma from migraine; and having to work harder than most people because of my disease. Next…
Read MoreLight a Candle to #ShineALight
June is National Migraine & Headache Awareness Month (#MHAM). Awareness months and dates are vital to: educate our community about headache and migraine disease; and fight the stigma associated with headache and migraine disease. Remembrance Day, which is observed on June 7, is especially meaningful for me. My parents and I lost our daughter and…
Read MoreAdvocating for Veterans: Operation Brainstorm
This Migraine and Headache Awareness Month, the National Headache Foundation and our partner organizations turn our attention toward the barriers to care that millions of Americans face trying to treat headache and migraine disorders. This problem is especially acute for U.S. service members and veterans. Studies show that veterans are more likely to develop migraine…
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