June is National Migraine & Headache Awareness month.
In June, the migraine and headache communities come together to raise awareness and recognition of migraines and headaches as debilitating diseases. June is also a time to encourage people suffering in silence to find a specialist or a doctor to help them. It’s a month to talk about current treatment options and new ones that are being created. It’s a time to celebrate how far the community has come in the past few years.
One of the hardest parts about having chronic migraines is feeling alone and misunderstood. I really struggled trying to fit in while being in constant pain until I found the migraine community. Now I feel like I have people in my life who understand how I’m feeling and who I can turn to with questions.
I wrote about my migraine story in 2018 and a lot has changed since then. The biggest thing that has changed is that I learned to advocate for myself. Instead of staying with a neurologist who pushed the same medication over and over I found a new neurologist who actually listens to me. I have so many more treatment options and I feel like a whole new world has been opened up to me.
I have put so many medications and treatments into my body in hopes of treating my migraines. I have had horrific side effects and have been sick for months because of these medications. I’ve gained weight, lost weight, and felt really crummy. I’ve tried diets, physical therapy, and different doctors. There is no cure but there is always hope.
I’ll be talking about migraines and headaches a lot this month. I never expected to find a migraine community through blogging but I have. Blogging about my migraine journey has been really beneficial for me and I hope I’ve been able to help others know that they are not alone in this.