HI 🙂 My EMG showed "diffuse myotonia" and my neurologist said that he did not see any issue with my nerves that would be causing my sensory issues. I will have the results from my genetic testing in about 5 weeks, so I guess I'm just waiting until then to determine my next move on this journey, but I feel like having a community, especially someone with potentially a similar diagnosis will make this easier! I currently take Cymbalta for my leg pain, it just started it a few months ago, it has helped but I have noticed that with the recent change in weather my symptoms are worsening, especially my pain. Please feel free to reach out to me at anytime! It is so nice to know that I am not alone! Even if we don't end up having the same diagnosis, it is nice to know someone out there has similar symptoms!