Finished ippi

Forums General Melanoma Community Finished ippi

  • Post
    gregor913
    Participant
      Hello, I finished ippi in april. After treatment I have a rash on each foot and small blotches on my legs still. None of them hurt or itch. I feel good . Was just wondering if this is something that is troubling? Cheers greg
    Viewing 11 reply threads
    • Replies
        jennunicorn
        Participant

          Glad you made it through Greg! Not sure about the rash and blotches, probably not super troubling but if it worries you just let your doc know. My legs get super itchy these days but with no rash… and my last infusion was in Feb! (I go back in 2 weeks to start maintanence doses… hopefully those go smoothly too).

          All the best,

          jennunicorn
          Participant

            Glad you made it through Greg! Not sure about the rash and blotches, probably not super troubling but if it worries you just let your doc know. My legs get super itchy these days but with no rash… and my last infusion was in Feb! (I go back in 2 weeks to start maintanence doses… hopefully those go smoothly too).

            All the best,

            jennunicorn
            Participant

              Glad you made it through Greg! Not sure about the rash and blotches, probably not super troubling but if it worries you just let your doc know. My legs get super itchy these days but with no rash… and my last infusion was in Feb! (I go back in 2 weeks to start maintanence doses… hopefully those go smoothly too).

              All the best,

              MoiraM
              Participant

                I used 1% hydrocortisone cream to get rid of my rash after Ipi.

                I confess I found my GP (general practitioner) and the melanoma specialist nurse much more helpful than my oncologist about the 'little stuff' that hung on after Ipi treatment.

                Firsty, I got a major flare up of side effects two months later, so be aware that can happen.

                Second, I never really sorted out the diarrhoea – it was like I had developed Irritable Bowel Syndrome. My GP helped me modify my diet and I cope just fine with it now, although I take a lot of deitary supplements!

                MoiraM
                Participant

                  I used 1% hydrocortisone cream to get rid of my rash after Ipi.

                  I confess I found my GP (general practitioner) and the melanoma specialist nurse much more helpful than my oncologist about the 'little stuff' that hung on after Ipi treatment.

                  Firsty, I got a major flare up of side effects two months later, so be aware that can happen.

                  Second, I never really sorted out the diarrhoea – it was like I had developed Irritable Bowel Syndrome. My GP helped me modify my diet and I cope just fine with it now, although I take a lot of deitary supplements!

                  MoiraM
                  Participant

                    I used 1% hydrocortisone cream to get rid of my rash after Ipi.

                    I confess I found my GP (general practitioner) and the melanoma specialist nurse much more helpful than my oncologist about the 'little stuff' that hung on after Ipi treatment.

                    Firsty, I got a major flare up of side effects two months later, so be aware that can happen.

                    Second, I never really sorted out the diarrhoea – it was like I had developed Irritable Bowel Syndrome. My GP helped me modify my diet and I cope just fine with it now, although I take a lot of deitary supplements!

                    keepthefaith11
                    Participant
                      My dad could only have two infusions before having to discontinue. He was on steroids for 6 weeks. Finished the steroids about two weeks ago. Now he has an itch on lower legs and arms. Not too bad but it’s definitely there. Assuming it’s from the drug. To me it’s a good thing because it shows the drug is still doing its job.
                      keepthefaith11
                      Participant
                        My dad could only have two infusions before having to discontinue. He was on steroids for 6 weeks. Finished the steroids about two weeks ago. Now he has an itch on lower legs and arms. Not too bad but it’s definitely there. Assuming it’s from the drug. To me it’s a good thing because it shows the drug is still doing its job.
                        keepthefaith11
                        Participant
                          My dad could only have two infusions before having to discontinue. He was on steroids for 6 weeks. Finished the steroids about two weeks ago. Now he has an itch on lower legs and arms. Not too bad but it’s definitely there. Assuming it’s from the drug. To me it’s a good thing because it shows the drug is still doing its job.
                          JuTMSY4
                          Participant

                            Did Ipi and then Pembro.  

                            After ipi, I had basically no side effects.  Pain from bone tumors went away (yay).  Did not show reduction though (suggestive of swelling, we pushed for pembro anyway, Doc was very supportive).  

                            Just had Pembro #19 (I think).  I've always had dry skin issues, mostly on my hands.  I've developed very dry hands and patchy dry feet now.  I've had that since about September October of last year (2015).  

                            Docs provided some topical steroids, which have helped (Clobetasol), but I try to limit use as they can be damaging to skin long term.  I've gotten to a decent managed point using extra-greasy eucerin and nitrile gloves at night.  Still gets itchy during the day.  
                             

                            Probably not troubling, but something to keep the docs aprised of and work with staff (nurses or your derm) to control.  It is most likely not a big deal, but I always like (and suggest) you tell your docs about any changes.  

                            JuTMSY4
                            Participant

                              Did Ipi and then Pembro.  

                              After ipi, I had basically no side effects.  Pain from bone tumors went away (yay).  Did not show reduction though (suggestive of swelling, we pushed for pembro anyway, Doc was very supportive).  

                              Just had Pembro #19 (I think).  I've always had dry skin issues, mostly on my hands.  I've developed very dry hands and patchy dry feet now.  I've had that since about September October of last year (2015).  

                              Docs provided some topical steroids, which have helped (Clobetasol), but I try to limit use as they can be damaging to skin long term.  I've gotten to a decent managed point using extra-greasy eucerin and nitrile gloves at night.  Still gets itchy during the day.  
                               

                              Probably not troubling, but something to keep the docs aprised of and work with staff (nurses or your derm) to control.  It is most likely not a big deal, but I always like (and suggest) you tell your docs about any changes.  

                              JuTMSY4
                              Participant

                                Did Ipi and then Pembro.  

                                After ipi, I had basically no side effects.  Pain from bone tumors went away (yay).  Did not show reduction though (suggestive of swelling, we pushed for pembro anyway, Doc was very supportive).  

                                Just had Pembro #19 (I think).  I've always had dry skin issues, mostly on my hands.  I've developed very dry hands and patchy dry feet now.  I've had that since about September October of last year (2015).  

                                Docs provided some topical steroids, which have helped (Clobetasol), but I try to limit use as they can be damaging to skin long term.  I've gotten to a decent managed point using extra-greasy eucerin and nitrile gloves at night.  Still gets itchy during the day.  
                                 

                                Probably not troubling, but something to keep the docs aprised of and work with staff (nurses or your derm) to control.  It is most likely not a big deal, but I always like (and suggest) you tell your docs about any changes.  

                            Viewing 11 reply threads
                            • You must be logged in to reply to this topic.
                            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