MELANOMA INTERNATIONAL FOUNDATION
July 13, 2012
I was diagnosed with MM in 2010, I was very scared by the word Malignant already dealing with CLL (Chronic Lymphocytic Leukemia) I searched on the internet for some realistic advise and understanding on MM and what I should be asking and expecting. With the of MIF I gathered a better understanding and it made the anxiety somewhat less. I knew if I didn't understand I could ask there and they would help me. I knew to ask about a sentinel node biopsy (came back clear) and they explained what a WLE was. Never was I made to feel that a question was dumb, or trivial I still go back and read, knowing that CLL especially now after Chemo Therapy can predispose me for skin cancers...Thank you for your time...Gillian Capewell
I've personally experienced the results of this organization in...
2010 when I was diagnosed MM they were a god send in their information and help
How would you describe the help you got from this organization?
How likely are you to recommend this organization to a friend?
How do you feel you were treated by this organization?
When was your last experience with this nonprofit?
How did you find this group?
google on the internet
What, if any, change in your life has this group encouraged?
I have never been a sun worshiper and have always used sunscreen but now I also advocate its use on my FB along with saying no to tanning beds