Morphea
Was wondering if anyone on here has Morphea (localized Scleroderma)? I know this isn't the right area, but I'm new, so I'm hoping you'll forgive me. If you have Morphea, were you able to get lap band? I'm scheduled for an orientation for WLS in May, and I'm hearing different things about whether this is an option for me... Thanks, Kit
I am new to this site. I was diagnosed with morphea 10 years ago. My lesion went away and the morphea has not been active since that time. I want to have lap band surgery as well. My doctor is currently researching whether I can be a candidate for lap band surgery. I will follow up when I get those results from him. In the meantime, I would also appreciate hearing if anyone else has had experience with this. You may also reach me at [email protected].
Thank you,
Laura
Great News! I just got a call from my WLS doctor and he said that I am approved for surgery. Dr. Broussard consulted with a rheumatologist and since morphea is not systemic (limited only to the skin) that lap band surgery is ok for those with morphea. Good luck and keep us all informed of how everything goes for you.
Laura