← Return to Has anyone had Paget's disease of the vulva?

Discussion

Has anyone had Paget's disease of the vulva?

Gynecologic Cancers | Last Active: Sep 27 8:18am | Replies (142)

Comment receiving replies
@juju67

Thank you so very much for sharing. I know it isn’t easy to talk with complete strangers about this disease. I feel very blessed to be in an area with a top notch Cancer center and to have a doctor who is a specialist. My Pagets is invasive and I was onboard with the surgeon to remove all that was present, including sentinel lymph nodes in both sides of my groin. The surgery is not easy, but he was able to get clear margins with no skin grafts.
I have a post op appointment tomorrow (I might be able to have the drains removed!).
I do have someone to help me at home; preparing meals, cleaning, so that is a huge help to me. I commend you for being able to take care of yourself alone. I know that is tough.
Thank you again for your input! I hope you can find some relief from the pain soon.

Jump to this post


Replies to "Thank you so very much for sharing. I know it isn’t easy to talk with complete..."

Was it non-invasive (did you know about it?) for a long time? I couldn't even remember the term for skin grafts as it is so awful - so huge - if I were to go that route. Also --- so wherever you are, the surgeon knows about it and is even a specialist! I'm envious 😉 Though my surgeons are good, I don't think they have experience with it.. .

Would you be willing to share your Dr and Cancer Center with us? It seems a dream to find a specialist. Our journey continues. I am grateful for each day and for this group.