I am feeling very low. Anna’s boyfriend came this morning with a van to move the rest of Anna’s things to her new flat. I find it difficult going up there and seeing it nearly empty.
The post has just come. I receive copies of all the letters my transplant consultant writes to my GP and other specialists. It was difficult to read that he “has a strong suspicion that there has been a relapse”. I know that if a relapse occurs within 12 months of a transplant that there are few options. If a transplant fails it is possible to have another one, but this one hasn’t failed as such; it may just not have prevented the mantle cell lymphoma returning.
This weekend my throat swelled up even more so I am particularly worried. I go to see the ENT consultant on Wednesday afternoon but I very much doubt if he can give me a definitive answer.
Throughout the months since I was diagnosed in 2007 there have always been further treatments and fall-back positions, then there was the hope offered by the transplant. I have pinned everything on the transplant and that hope is easily destroyed. It may be that all of this inflammation is related to GVHD but I am not so sure it is likely as that would happen to everyone else who had GVHD and that is 50% of all bone marrow transplant patients.
For the first time I feel totally helpless. I know this must have happened to other transplant patients but I don’t know much about what happens now. I must just wait for events to unfold and hope against hope.
I'm so sorry. That does sound very difficult to cope with. I'm holding out for good news and thinking of you!
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