Hello,
I have a couple of questions and would really appreciate any insight from those who may have experienced something similar.
1.) I’ve noticed that my flares have become both more frequent and more intense, particularly in my hands. What’s changed recently is that the burning sensation is now accompanied by a persistent dull ache. I understand that symptoms can vary widely between individuals, but I’m wondering: has anyone else experienced this kind of shift? In the past, I could tolerate the burning to some extent, but now the intensity and the aching that comes with it have become extremely painful and harder to manage.
2.) My naturopath, who is helping me with other health issues, has been researching EM to better understand it, given how rare it is. In her research, she came across a few articles suggesting a potential link between long usage of SSRIs, specifically Zoloft (Sertraline), and the onset or worsening of EM symptoms. Some individuals reportedly developed EM after starting Zoloft, while others noticed improvements after tapering off. Interestingly, there are also cases where symptoms worsened after discontinuation and then improved again once the SSRI was reintroduced.
I’ve been on Zoloft since 2005, and my naturopath believes this is worth exploring. Has anyone here heard of/or had any experience with Zoloft or other SSRIs in relation to EM?
Thank you in advance for any insight or experiences you’re willing to share.