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maryb-z

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      maryb-z
      Participant
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        maryb-z
        Participant
          Hello! I had Imlygic/T-Vec therapy a few years ago. It was not successful and I ended up doing 2 years of Opdivo.
          maryb-z
          Participant
            Hi Isaac,

            I was treated with TVEC in 2017 for 3 tumors in my lower leg. I remained stable for a short time-5 months and then was on Opdivo for 2 years. I wish your wife much luck!

            maryb-z
            Participant

              I did not qualify for the 3rd shot as I am no longer on steroids or any treatment. I do teach over 500 kiddos a week but that’s not a qualifier. I will be wearing a mask.

              maryb-z
              Participant
                Although not NED for 5 years I am still here 12 years after being diagnosed. Lots of recurrences, surgeries, interferon, clinical trial, T-vec and most recently completed 2 years of Opdivo. Grateful for all the bonus time.
                maryb-z
                Participant
                  Hi!

                  Nodular melanoma diagnosis 2009 with at least 8 recurrences-I lost count. I completed 2 years Opdivo October 2020. My November scan showed no active disease but I have learned how sneaky melanoma can be. No organ involvement just all over my right leg.  Just stay vigilant. Grateful for all my BONUS time.

                  maryb-z
                  Participant
                    Hello!
                    I have been dealing with this disease since 2009. I just completed 2 years of Opdivo. I tried the monthly dose but my body could not handle it so twice a month at half the dose was decided. I’m so glad I have my port as after interferon my veins went to crap. I plan on keeping it for another year and get it flushed monthly. I’ve had 8+ recurrences so I am.keeping port in case. Through my 2 years of treatment I’ve had PET scans every 6 months to ensure Opdivo was doing its job. My melanoma specialist wants to follow me closely and never uses the terms cancer free. I’m currently. NED but with my history of recurrences I’ll be monitored for the rest of my life. I’m stage 3C. Every doctor is so different on how often to scan and using CT versus PET. One doctor only wanted PET and only a year of Opdivo. Another feels CT is sufficient and 2 years treatment. I opted for 2 years of treatment and PET scans. Best of luck to you!
                    maryb-z
                    Participant
                      I had 3 tumors in my right leg that responded well to T-Vec, in fact they were annihilated. Unfortunately a year later I had another tumor pop up so I am going on year 2 of Opdivo.
                      As far as pain I’d say it was uncomfortable but the team in the room talked to me the whole time and that helped keep my mind off the injections. Best of luck to you!
                      maryb-z
                      Participant
                        I get full body PET/CT scans as all my recurrences have been on my lower leg. Many of my lesions over the past 11 years have been found by PET/CT.
                        maryb-z
                        Participant
                          My 11 year cancerversary is February 11th. I did do one month high dose interferon in 2009. I have had several recurrences., surgeries, one clinical trial, T- vec injections, and now I’m on Opdivo. I’m stage 3C and have had over 20 PET/CT, and MRIs. It’s the gift that keeps on giving. Rollercoaster ride is an understatement.
                          maryb-z
                          Participant
                            I opted for a port due to terrible veins. Best decision. I tried the monthly infusion but my joints became inflamed and calcium levels skyrocketed. Went to 2 twice monthly infusions which helped decrease side effects but I also needed 5mg prednisone for inflammation. I also did treatments for 2 years. I’m stage 3C and have had 8 recurrences in 11 years. Best of luck!
                            maryb-z
                            Participant
                              Hi Ted!
                              My melanoma specialist is recommending I teach remotely. I sent his email on to admin and am waiting for a response.
                              maryb-z
                              Participant
                                Thank you for responding, Ted! UW Health (I’m in WI) has a prototype mask/shield combo that I think would work great for teachers. It’s being tested and I’m not sure when or if it will be made available to purchase. https://www.facebook.com/56887600728/posts/10158339149945729/

                                I’m just so anxious as I need my job for the health insurance so I can’t just work anywhere. I’ve been teaching for 30 years. I didn’t work so hard fending off cancer only to be killed by Co-vid.

                                maryb-z
                                Participant
                                  Thank you to everyone who took the time to respond to my post. I have not made a decision yet. I have until October. I am one who takes my time with making decisions in all aspects of my life. I have had 11 years of dealing with this disease and realize whatever I decide is the choice I make for me and not influenced by my loved ones. So much is a crap shoot with melanoma. So grateful for this forum. Thanks again!
                                  maryb-z
                                  Participant
                                    Hi!
                                    I’ve been dealing with this beast for 11 years. As I write this I am getting my Opdivo treatment. I almost had to quit back in January 2019 because I had the less frequent side effects of swelling and severe joint pain. I saw an endocrinologist and rheumatologist. In the end a prominent melanoma specialist was contacted and he prescribed a low dose of prednisone (5mg). Made a world of difference and the prednisone does not negate the effects of Opdivo in low doses. Good luck!
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