Hi @1Familyrus, and welcome to the Sjogren’s Syndrome patient support group. I’m Julie, a Ben’s Friends intern. I’m so sorry to hear about how rough it has been for you with Sjogren’s so far. It must be stressful how many different things an autoimmune condition can cause, but I’m glad that you were able to find this board. Many others on this board have suffered from hair loss, rash, dry eye, along with a mix of other symptoms associated with Sjogren’s syndrome, so feel free to type in keywords to search through past discussions using the magnifying glass at the top of the page. Some discussions may not have been active for quite some time, but if you would like to hear how others are doing (or let us know how you’re doing, yourself) you can start a fresh conversation by clicking the ‘+New Topic’ button and letting us know what’s on your mind.
Otherwise, the other mods (members with a shield next to their names) and I are here to help you navigate the website or get involved with discussions! You can privately message any of us by clicking our username and then clicking ‘Message’ if there is anything you need. Hope to hear from you soon, and welcome again to the Sjogren’s Syndrome patient support group 