Petal's Place

Howdy, there. I'm still trying to get the word out for my hidradenitis suppurativa support group. The support group is for peers living with hs by peers living with hs, which we acknowledge might not be everyone's thang, but if it is yours please read on. www.therecystance.org What can I do to help if I don't have HS? - Rebloging and engaging helps us get the word out immensely. If you jive with the tenets we use, like mutual aid, then please, consider helping us get out there. - Or, if you know someone with HS, consider gently telling them about our support group. --------- The Recystance is a prospective mutual aid organization for the hidradenitis community. You are free to apply to join our group (if you meet the conditions) via the website. All details are there. We aren't a scam or backed by some brand that wants to sell salve, we really are a honest-to-god group based on mutual aid and inclusivity.

Howdy, there. This post is for hidradenitis suppurativa havers, so if you've seen it and you don't have HS: no u didnt. www.therecystance.org The Recystance is a prospective mutual aid organization for the hidradenitis community. Our first goal, which may interest you, is to launch a support group. You are free to apply to join this group (if you meet the conditions) via the website. All details are there. We aren't a scam or backed by some brand that wants to sell salve, we really are a honest-to-god group based on mutual aid and inclusivity.