Have any CLL patients had Mohs surgery at MD Anderson? How was your experience? TIA
Mohs Skin Surgery : Have any CLL... - CLL America Support
Mohs Skin Surgery
![ElmTree71 profile image](https://images.hu-production.be/avatars/4202735c-8056-45cb-80db-485e489b0e0e_small@2x_100x100.jpg)
![ElmTree71 profile image](https://images.hu-production.be/avatars/4202735c-8056-45cb-80db-485e489b0e0e_small@2x_100x100.jpg)
ElmTree, If you select the text below your post;
"*This community is not currently active*
We are looking for a new patient organisation for this community. Please join the active CLL Support",
that will take you to an active CLL support community where you are far more likely to have a response.
Neil
I had Mohs surgery 3 times. When they took it off my ear and leg they would remove some and then I had to wait to see if they took enough out. They had to go back a second time and take a little more until they were satisfied that they had removed all of it. When I had my nose done I was given a sedative and went to sleep. I had it done in Boston. Good luck with the surgery!🦋
It sounds like a difficult place to have it. Please take care and I hope your healing goes quickly!🥰