Anyone out there have their LP correlated to GLP1, specifically Zepbound? Doc says it’s rare but they are seeing new cases popping up more and more.
Obviously I will stop taking it so we’ll see in about 6-8 weeks if my rashes improve. I sure hope so.
I can’t even begin to start with all the money I’ve spent on products … either over the counter or the ads that come up on my social feeds constantly or the natural remedies people swear by … and nothing has actually helped flatten out or stop the spread of this. I have it on my hands and feet but also patches all over my body. I have a follow up doctor appt soon and I really don’t want to be put on any of these prescriptions because they all seem to have horrible side effects or risks of cancer associated with them. I am currently on Dupixent (for about 6/7 weeks so far) because I actually have eczema and asthma too but I don’t know if it helps with skin LP.
I have a history of eczema but it has seriously flared up a few months ago and while doing so I started getting another rash on my hands, wrists, arms, feet. It was misdiagnosed by a dermatologist PA as all eczema this was after multiple other medical providers (PC and urgent care) thought it was something else too. I had a second opinion derm appointment last week and she said it looks like Lichen Planus and eczema and maybe something else uhg! She took samples for a biopsy. I am super itchy and skin is bumpy and dry all over my shoulder, back and thighs. It’s miserable. I was put on Dupixent, it’s been 4 weeks with only some very minimal relief. Just hoping to hear from others who may be dealing with multiple flares and what are you doing to heal and cope?