MPIP: Melanoma Patients Information Page

The MPIP is the oldest and largest community of people affected by melanoma hosted through the Melanoma Research Foundation. It is designed to provide support and information to caregivers, patients, family and friends. Once you have been touched by melanoma—either as a patient or as a family member or friend of a patient—you become part of a community. It is not a community anyone joins willingly. But if you must be part of this group, you will find no better place to find the tools you need in your journey with this cancer, and the friends who can make that journey more bearable.

The information on the bulletin board is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

Jenna - NED for eternity

I am very sad to tell you that Jenna passed away over the weekend at the age of 20. 

FDA delay

Have you noted that FDA has delayed the approval of Ipilimumab by 3 months.  I suppose they all want to go on vacation with our president, while some of us stay home and suffer.   Since I can't get into a clinical trial, I was waiting for Ipili to be approved for my Dr. to use possibly. I am the one with heart disease also.

Stage IV..Roll Call for the Undead Please

Been a lot of dying going on around here due to melanoma  of late, but there is also a lot of living going on as well.

For those of you that don't know me, please do not think I am being cavalier about people dying from melanoma.  My girlfriend died in my arms as a result of melanoma(who I met from here by the way).  I have been Stage IV melanoma since 1996 and was Stage III 9 years before that and am now in my 8th recurrence as I am in the middle of my 23rd year since diagnosis with an unknown primary.

Another skull crack coming up :)

Not around often these days- I've found it's better for my health if I remain only a rare visitor :P

Just a heads up for those interested. Had scan yesterday, am getting organised today, flying back tomorrow and having another craniotomy Thursday (Oz time). Feeling very happy and relaxed about it all. Looks like it will be a re-excision of a previous right frontal tumour, so hopefully same bone flap will be used and I can keep my separate sites limited to 6 (ROFL!)

food for recovery

need for suggestens for recovery from surgery

food for recovery

need for suggestens for recovery from surgery

MOFFITT area MPIP'ers... i need your help!

Hi!! I am in desperate need of a wheelchair for a few weeks to months and was hoping that someone in the tampa / moffitt hopital area has an old one they would let me have for a while.  if not, does anyone know where i can get one donated or for cheap?

this is not for me, but a family member who is unable to walk right now due to an accident.

 

thank you for your help with this.

 

Djpayn (dawna)

Survivors

I am 30 years old and was diagnosed with melanoma in June 2010. Over the summer, I had a WLE and SNB. One of the lymph nodes had microscopic melanoma in it. I then had a lymph node dissection of my left groin in August. Luckily, those lymph nodes were clean. I am stage 3a. In September and October, I went through the induction phase of Interferon and now am in the maintainence phase. I am lucky to not have many side effects and am working full time.

Failed Bio-Chemo Need Advise on PD-1 Antibody Combo

 

I did the 6 rounds of Bio-Chemo things were shrinking well, then went on the maintenance part, did 2 rounds of maintenance then scans showed developed new tumors in the liver. There are multiple new lesions laterally in the liver in segment 8 there are new lesions in segment 5 and 6 as well. Existing tumors were stable or shrinking a little.

Dr. Weber advised I go on the PD-1 Antibody Combo Trial. There will not be any openings until 4 weeks pass, so I am getting worried about waiting so long before I can jump into treatment.

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