Nausea – just started taking Entocort

Forums General Melanoma Community Nausea – just started taking Entocort

  • Post
    Lisa13
    Participant

      As dicussed before, I was having some issues which at first scared me, but then my oncologist perscribed me the entocort and immodium, Today I just started the Entocort because I was feeling nauseus.  I know the internet says that nausea is normal with crohns disease and just wanted to know if anyone has experienced the nausea with this problem?   It's very mild nausea and comes and goes. Because of this, I don't have much of an appetite which is completely understandable. 

      As dicussed before, I was having some issues which at first scared me, but then my oncologist perscribed me the entocort and immodium, Today I just started the Entocort because I was feeling nauseus.  I know the internet says that nausea is normal with crohns disease and just wanted to know if anyone has experienced the nausea with this problem?   It's very mild nausea and comes and goes. Because of this, I don't have much of an appetite which is completely understandable. 

      I just want to know if this is what others have experienced. When I asked my Dr. why he's just giving me a perscription and not concerned about the cancer, he said that the symptoms I was having was colitis.   Since way before cancer, I've had acid reflux and hiatal hernia which have become worse since all my treatment, so it's hard to know what the heck is happening.  Having cancer, anything bothers you even though it could be completely normal.

      Isn't it strange how I had no symptoms while on ipi (except for rash and itching) and now, 3 months after finshing, I've got the rash, itchy head, intestinal problems and nausea!  My immune system is definately kicking in again!

    Viewing 2 reply threads
    • Replies
        Roxy1453
        Participant
          I’m only on my second round of IPI and I’m having a lot of side effects. When I had the scope done yesterday they said in the OR that it was a good sign the the IPI was working. So even though it has been 3 months for you, I hope it means it’s working for you too!
            Lisa13
            Participant

              Some people have late immune responses, so this is very normal what I'm going through.

              When I finished ipi, I had a 12 week and 16 week scanned which showed 50% shrinkage in lung mets and some even disappeared. My next ct scan is in 2 weeks, so I hope things are still looking great.

              I hope that when you're done ipi and have your scans, that things look great for you!

              Lisa

              Lisa13
              Participant

                Some people have late immune responses, so this is very normal what I'm going through.

                When I finished ipi, I had a 12 week and 16 week scanned which showed 50% shrinkage in lung mets and some even disappeared. My next ct scan is in 2 weeks, so I hope things are still looking great.

                I hope that when you're done ipi and have your scans, that things look great for you!

                Lisa

                Lisa13
                Participant

                  Some people have late immune responses, so this is very normal what I'm going through.

                  When I finished ipi, I had a 12 week and 16 week scanned which showed 50% shrinkage in lung mets and some even disappeared. My next ct scan is in 2 weeks, so I hope things are still looking great.

                  I hope that when you're done ipi and have your scans, that things look great for you!

                  Lisa

                Roxy1453
                Participant
                  I’m only on my second round of IPI and I’m having a lot of side effects. When I had the scope done yesterday they said in the OR that it was a good sign the the IPI was working. So even though it has been 3 months for you, I hope it means it’s working for you too!
                  Roxy1453
                  Participant
                    I’m only on my second round of IPI and I’m having a lot of side effects. When I had the scope done yesterday they said in the OR that it was a good sign the the IPI was working. So even though it has been 3 months for you, I hope it means it’s working for you too!
                Viewing 2 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