Dear Doctors & Researchers

Dear doctors, researchers and drug companies:

This is an open letter to any and all medical professionals. My wife is one of many people suffering (immensely) with a rare disorder called erythromelalgia. Just a small amount of research into this condition confirms what every EM sufferer knows too well: It’s incredibly painful, impossible to predict, and has no known cause or cure. It completely controls and destroys the sufferer’s quality of life. It is an extremely frustrating spot to be in.

The purpose of this letter is to bring awareness to this condition and its sufferers. I understand that it’s rare, which lessens (or eliminates) the chance of research being paid for and conducted by large research institutions and drug companies. So, I’m asking that some company or individual look past that and decide to put research into this disease—for all those in inexplicable pain. And who knows, along with helping them you may find a way to treat other pain disorders.

Again, I don’t have EM but I understand the pain since my wife suffers with it. And I would do anything to make her well. Please help.


P.S. To any and all those already researching and trying to cure EM, we thank you!


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