The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Liberte121

Forum Replies Created

Viewing 0 reply threads
  • Replies
      Liberte121
      Participant

        Summer – I am a stage 4 melanoma patient since May 2016. ( ialso also am fighting lymphoma and fought Bladder cancer in this same time period)I have tried Yervoy, but had to discontinued due to liver toxcity numers, Tried Keytuda, same thing. I have been on Zelboraf and Cotellic now since April 2017. at first we started REAL slow, and I am now at 3 tablets of Zelboraf in the morning and 3 at night with 2 Cotellic. Up until September of this year, I was having nausea, fatigue, pain in my legs and just felt like crap.

        However, we fought my lymphoma this September. My bladder cancer is gone, my lymphoma is stable and my melanoma is stable with zero indications on my scans. TheZelboraf and Cotellic have been  God send. I do not have any symptoms at all. I am now more physically active, and I am regaining my strength.

        My doctor(s) have all told me from early on to stay active – even when you do not feel like it, and that has been a huse reason for success. I havea tee time schedule for January 1st at 11:00 ,( I do cover all my skin as a get sunburned otherswise – even taping over the holes on my golf gloves.

        Best advice is to talk with your doctors for managment of her side effects. eventually they will be managable or go away

        BE POSITIVE AND STAY STRONG. WE CAN BEAT THIS

        Tim G

    Viewing 0 reply threads
    About the MRF Patient Forum

    The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

    The information on the forum 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.

    Popular Topics