Do you have any local support groups for hyperhidrosis? I mean, local as in Real Life. 🙂
I have a friend who, just like me, suffers from hyperhidrosis. Since there are two of us, we thought how it would be great if we could muster up some courage and start some kind of local support group for hyperhidrosis.
We would essentially like it to be like an informal book club (lol), only we would talk about our struggles with hyperhidrosis instead. Ideally, we could even exchange iontophoresis machines or other useful equipment, remedies, and so on. E.g. we have Idromed and Drionic, while others could have Fischer Galvanic and Hidrex, etc. Maybe by exchanging our devices with a group of friends we could try out what works best for free!
But even more important is the exchange of advices, tips, and most of all, understanding and support.
The only problem is, I don’t know how to go about it. At the moment, this seems like a big project – I’m not sure if there are any legal requirements. Do we need to register these meetings somehow, or can it be completely informal?
If you have similar local support groups, and know how to start one and how these things work, please share your knowledge with me. Thank you!
