Someone shared their heart on Facebook, via Fibromyalgia Network, and I wanted to share it. Although not HKPP, I did receive an incorrect diagnosis of FMS when I was a teen. The symptoms are eerily similar, and this lady's rant describes my life in every way. I imagine it applies to all with Periodic Paralysis as well as other systemic diseases. I believe everyone can learn something from this.
Feel free to pass it on.