Avoiding the use of humidifiers (which often grow bacteria).Avoiding moldy areas (such as a damp basement).Avoiding heavy cleaning (and other) chores such as vacuuming for several months after the transplant.Employing the help of someone (whenever possible) to keep the bathroom and other areas of the home clean and disinfected.Keeping the home environment clean and as dirt/dust-free as possible (without going to extremes).Reporting any problems with the central catheter (such as a break or leak in the catheter, redness, swelling, pain or other signs of infection at the catheter site).Performing central catheter care as taught by the nurse on the transplant team.Avoiding any type of body piercing or tattoos (which can increase the risk of infections such as hepatitis, skin infections or other types of infection).Limiting the time in the sun and using sunblock (the skin may burn more easily after a transplant procedure).Getting re-immunized with childhood vaccines (usually about a year after the transplant procedure).Reporting signs of bleeding (from low platelet count) such as frequent bruising or nosebleeds, bleeding gums, petechiae (tiny purplish dots on the skin) or other symptoms.Reporting a fever of 100.4 or higher or any other signs and symptoms of infection.Mouth care using a soft toothbrush until the platelet (blood clotting) cell count is high enough.Frequent handwashing and good personal hygiene.Bathing and washing with antibacterial soap.Eating a special diet that supports the immune system and avoids food that may harbor germs that could cause an infection. Avoiding public places that are highly populated, using a mask when necessary.It was unbelievably frustrating because the three things that doctors are constantly telling you to do after transplant is to move around, go for walks, and eat and drink, drink, drink water, water, water, water, water, like they are measuring how much water and food intake and exercise I’m doing every single day. It resolved itself.Īfter about a week, it got slowly better. So I couldn’t speak and I had a very difficult time swallowing. They did give me one type of chemo that is very much I don’t remember the name, but it’s very much known for creating mouth sores and I had mouth sores all the way down inside my throat. I did have mouth sores, which with high dose chemo and many other types of chemo is common. Lots of upset stomach, I did not want to eat. The steroids also made me feel a little bit weird. The side effects were very similar to the chemo and more than anything else, that was the chemo that I was feeling side effects for more than the transplant. Here’s what some cancer patients have to share about their personal experiences and what to expect after stem cell transplant: Patients often report a strong smell of creamed corn or garlic in the room or in their mouth. If an oncologist or other healthcare provider has recommended, SCT for you or a loved one, you may wonder about what to expect after stem cell transplant. Miklos What to expect after stem cell transplant Maybe it’s a brother or sister or HLA-identical donor whose blood destroys the white cells, red cells, and regrows and reconstitutes the normal blood system. Some of your patients may have had an allogeneic transplant which is truly the immune therapy of someone else’s immune system. We’ve tried high-dose chemotherapy and I’m a stem cell transplanter, so the notion of using high-dose chemotherapy with stem cell rescue or what your patients will know as an auto transplant, has provided much benefit to the patients of mantle cell.
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