The
recovery stage begins after the stem cell infusion. During this time,
you and your family wait for the cells to engraft, or “take,” after
which they begin to multiply and make new blood cells. The time it takes
to start seeing a steady return to normal blood counts varies depending
on the patient and the transplant type, but it’s usually about 2 to 6
weeks. You’ll be in the hospital or visit the transplant center daily
for at least a few weeks. During the first couple of weeks you will have
low numbers of red and white blood cells and platelets. Right after
transplant, when your counts are the lowest, you may be given
antibiotics to help keep you from getting infections (this is called
prophylactic antibiotics). You may get a combination of anti-bacterial,
anti-fungal, and anti-viral drugs. These are usually given until your
white blood cell count reaches a certain level. Still, you can have
problems, such as infection from too few white blood cells
(neutropenia), or bleeding from too few platelets (thrombocytopenia).
Many patients have high fevers and need IV antibiotics to treat serious
infections. Transfusions of red blood cells and platelets are given
until the bone marrow is working again and new blood cells are being
made by the infused stem cells. Except for graft-versus-host disease,
which only happens with allogeneic transplants, the side effects from
autologous, allogeneic, and syngeneic stem cell transplants are much the
same. Problems may include gastrointestinal (GI) or stomach problems,
and heart, lung, liver or kidney problems. You might also go through
feelings of distress, anxiety, depression, joy, or anger. Adjusting
emotionally after the stem cells can be hard because of the length of
time you feel ill and isolated from others. Having a transplant is a big
decision. Your life and your relationships will be disrupted. Your
future becomes uncertain, the process makes you feel bad, and
financially it can be overwhelming. You might feel as if you are on an
emotional roller coaster during this time. Support and encouragement
from family, friends, and the transplant team are very important to get
you through the challenges of transplant.
This site is for information on the various Chemo treatments and Stem Cell Therapies since 1992. This journey became bitter sweet in 2014, with the passing of my beautiful and dear wife. Sherry, had fought Non - Hodgkins Lymphoma(NHL) since 1990, in and out of remissions time and time again. From T-Cell therapies(1990's) to Dual Cord Blood Transplant(2014), she was in Clinical Trials over the years. This site is for informational purpose only and is not to promote the use of certain therapies.
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