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@loribmt

☺️ My advice to you…from experience…trust your doctors on this. It’s not their first rodeo, though it’s yours. Learn to put the worry on their shoulders. (Yes it’s ok to question them! I’m not saying be complacent because knowledge is power. But they’re following you and responding in your best interest)
They’re obviously on this if they lowered the Cellcept to allow your own immune system to react and make those important antibodies to the CMV.
4 isn’t too strong…and it’s just ‘almost’ in range of normal and may be a good compromise for you. 2 is too low, you don’t want to live in perpetual neutropenia. Subsequent blood tests will let your team know how well you’re doing with the transplant.
Relax, you’re a year out! The critical stage is over so now it’s maintenance and you’re doing great!!! Deep breaths!!! Hugs!!! 😘

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Replies to "☺️ My advice to you…from experience…trust your doctors on this. It’s not their first rodeo, though..."

Lori,
Thank you so much for this caring and beautiful response! You know exactly how I am feeling and what I needed to hear. I can't thank you enough for being so loving. BIG Hugs right back to you!! .....And I am going to try to take your excellent advice and "breathe"! Love to you 🙂