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Anyone else have Mantle Cell Lymphoma?

Blood Cancers & Disorders | Last Active: 4 hours ago | Replies (94)
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@ffb1234

Lori, thank you. That is very kind and thoughtful of you. It has been a year that is for sure. My blood counts are still the same. Saw my BMT doctor last week for my anniversary checkup and she is concerned also. Doing a bunch more tests now. Hopefully we will get this figure out. Again thank you for your caring and kindness.

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Replies to "Lori, thank you. That is very kind and thoughtful of you. It has been a year..."
Lori, Volunteer Mentor | @loribmt | 4 hours ago

As you’re finding out, having a BMT changes everything! We’re given this amazing 2nd chance at life but with it can come some adaptions we’re not used to dealing with for sure!
Personally, I felt the first year was the most challenging. So, happy 1st Re-Birth day and best wishes for a much better year…years…ahead!!

I’d like to invite you to participate in some of our BMT/SCT conversations in the forum! I think you’ll enjoy getting to know some of the other Chimeras…we’re a special lot. Haha.

We share our experiences which can really help to let you know you’re not alone. That we all have little quirks with our newly acquired immune system and we’re here to support each other.
You’ll meet up with some regulars there and some newbies like @katgob who is just a little behind you in her journey.

These two discussions will be a good place to get started:

~My Bone Marrrow Transplant Story: Will you share yours?
https://connect.mayoclinic.org/discussion/my-bone-marrow-transplant-bmt-story-will-you-share-yours/
~Snapshots of hope: Life on the other side of transplant
https://connect.mayoclinic.org/discussion/snapshots-of-hope-life-on-the-other-side-of-transplant/
What did you do to celebrate your first BMT anniversary?

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