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8 Treatment Hacks for People With Migraine and ME/CFS

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One of my worst symptoms having ME/Lyme disease has been horrific migraines; everything from aching in the temples and burning pain in the base of my skull to throbbing in the crown of my head that made me black out when I stood up.

It’s been a long journey of experimenting with different treatments, which was made all the more challenging by the fact that migraines attributed to ME do not respond to normal migraine medication.

I’m eager to share some ways I’ve found relief from migraines with CFS/ME, in the hope that it might help someone reading this.

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