Help Christine raise money

Migraine, head pain and facial pain are constant in my life. I've lived with Migraine since 2008 managing at home with the help of my PCM because Headache Specialists are far and few between. Then in 2014, I was complaining about a single sided headache behind my right eye, imaging was done but there was 'no findings', the pain continued. In August of 2023 I finally said enough is enough, I was tired of the constant pain. At this point I had experienced this pain for 9 years.. I finally found a doctor who actually took the time to listen, she diagnosed me with Hemicrania Contunia. That medication took my pain away, it was magic, but that didn't come without side effects. In April of 2024 I was diagnosed with Trigeminal Neuralgia, again multiple medication trial and error plus the many side effects (we are still working out the kinks). In November of 2024 I had Microvascular Decompression Surgery at the UPenn, while it took all of the stabbing and shooting pain away, I still live with nearly constant facial burning and pins and needles. It continues to be a work in progress, however I love what Miles for Migraine is doing to help stop the stigma and increase research for people like me.