Vulva melanoma biopsy results...going stir crazy

Hi all,

.I noticed a couple of months ago brown like stain/patches on my vulva....that were never there before...i was sent for a biopsy after the dermatologist said  oh I think its nothing to worry about it looks likes melanoma. I received my biopsy appointed 4 days after dermatologist...Leading up to my biopsy I  noticed more small patches of this brown patch and were the main one was...when I pulled the skin a little tort I noticed white shading behind the area. There was a slight discomfort in the area before hand. Anyhow I have had my biopsy and now nervously waiting my results!! Does this sound like melanoma and is it really nothing to worry about?  I find myself trying to Google and find images to compare...i just want to know!!! I am.trying to be patient....it has only been 5 days and I was told it can take upto 6 weeks. 

  • Hello Hlou82

    I'm sorry to hear that you've had some health concerns recently and that you're now waiting on your biopsy results. We know that it can be a really difficult time waiting for news and it's understandable that you're feeling anxious. Please do try to give Google a wide berth as there is a lot of unreliable information online that won't give you firm answers about your situation but will leave you feeling more anxious about things. 

    We know that many people find that it helps to talk to someone at times like this and I wonder if you'd find it helpful to chat with one of our nruses. I'm sure they would be happy to listen and offer any advice, information, and support that they can ahead of your appointment. If you'd like to speak with them they're available Monday to Friday 9 am to 5 pm on 0808 800 4040. 

    Hopefully, you will have some news soon. Do let us know how you get on. 

    Best wishes, 
    Jenn
    Cancer Chat moderator 

  • Hi,

    I'm sorry you are going through this anxious time and now have a long wait for your results.

    I have no personal experience of vulva/mucosal melanoma as mine is on the skin (superficial spreading melanoma). This type of melanoma isn't common so hopefully your results will come back clear but if not, there are groups online for mucosal melanoma patients where you can get advice and information. 

    The best thing to do at the moment is to concentrate on keeping busy in order to distract your mind from worrying. Please don't Google as information on there is out of date and will only make you worry more. Chat to one of the nurses as Jenn suggests - it may help you deal with the stress until your results come back.

    Good luck and please let us know how you get on.

    Angie (Stage 3 melanoma patient since 2009)

  • Hi,

    I am being treated for a 'rare' mucosal melanoma does anyone know of any support groups out there ?

    thanks 

  • Hi did you get any answers to this I’m hoping you got the best possible outcome I am going through the same thing so would love to hear your experience