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@josettecedo

I’ve had MF since 5/23. So many things have happened to me. Would like to talk to someone who is going through the same as me.

Thank you,
Josette

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Replies to "I’ve had MF since 5/23. So many things have happened to me. Would like to talk..."

Hello
I am not sure if this platform is ok to disclose information but would like to ask you if you tried Brentuximab IV and extracorporeal electrophoresis?
Alice

Hi Josette. I have had CTCL - MF. Treatment depends on the stage of your disease. I have stage 1A. This is the first stage of the disease. I was diagnosed by a dermatologist and I am followed by oncologist as well. I see my dermatologist frequently 3 to 4 times a year. Because of the stage my treatment is UV light 3 times a week. I have a light box in my house so it is convenient. I am not on chemo or any other treatment. This does not mean I will not need chemo. Please feel free to ask other questions by replying directly to me.

I got diagnose on Dec 2022 . So not long ago. But no staging because they said only the skin was involve