Blood Donor: Is it safe to donate blood if you have a blood condition?

Posted by Diane Grant @dianegrant, Apr 25, 2023

Has anyone ever checked if it is safe to donate blood? I am O- and used to donate regularly. I was considering starting up again then got my diagnosis. My main concern is O- is used to sick babies and I wouldn't want to make them worse.

Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.

@gingerw

@nypara66 After my Systemic Lupus diagnosis in 1988, I was advised to not donate blood any longer. That was a sad time for me, as I also had just found out I was a match to be a bone marrow donor for someone in need. We decided it was in everyone's safety and best interest that my blood products not be considered. I would never want to knowingly donate an unsafe product, nor expose anyone to to less-than-perfect blood products!

In 2016 my husband received a deceased donor kidney. In the middle of 2017 his transplant team called him in a panic, as the other kidney recipient from the same donor had contracted Hepatitis C. Everyone was tested, and it was discovered the other kidney recipient had latent Hepatitis C. While they were relieved to find this out, the transplant team certainly had a scare, thinking their donor has passed something on to the recipients!
Ginger

Jump to this post

I would NEVER knowingly donate something that I knew was possibly unsafe for anyone. My husband is also a transplant recipient. He had a liver transplant. I’m happy yours was not given the Hep C kidney. That is unbelievable that that even happened. On a good note, they can now cure Hep C but the meds are 80k. I truly think my doctor just wanted me to “Dump” my blood before my final diagnosis because my hematocrit and platelets were crazy high. Insurance won’t cover phlebotomies until deemed medically necessary, meaning I had to have the diagnosis first.

REPLY
@nypara66

I would NEVER knowingly donate something that I knew was possibly unsafe for anyone. My husband is also a transplant recipient. He had a liver transplant. I’m happy yours was not given the Hep C kidney. That is unbelievable that that even happened. On a good note, they can now cure Hep C but the meds are 80k. I truly think my doctor just wanted me to “Dump” my blood before my final diagnosis because my hematocrit and platelets were crazy high. Insurance won’t cover phlebotomies until deemed medically necessary, meaning I had to have the diagnosis first.

Jump to this post

@nypara66 My husband's donor did not have Hep C. It turned out the other kidney recipient from the same donor, had latent Hep C, that was stirred up when he got his new kidney! So, the transplant team tested everyone to find where that hep c case came from.
Ginger

REPLY
@gingerw

@nypara66 My husband's donor did not have Hep C. It turned out the other kidney recipient from the same donor, had latent Hep C, that was stirred up when he got his new kidney! So, the transplant team tested everyone to find where that hep c case came from.
Ginger

Jump to this post

Wow that is some story! Hopefully he could get the meds and cure it but we both know about the intense drug regimen after transplant and it takes the body’s a long while to adjust to the meds. after surgery. My husband just had his 7 year anniversary last week and is doing well. I’m very grateful!

REPLY
@nypara66

Wow that is some story! Hopefully he could get the meds and cure it but we both know about the intense drug regimen after transplant and it takes the body’s a long while to adjust to the meds. after surgery. My husband just had his 7 year anniversary last week and is doing well. I’m very grateful!

Jump to this post

Congrats to your husband!
Ginger

REPLY

I have ET and take hydroxyurea. I was told no blood or organ donations ever.

REPLY
@gingerw

@dianegrant I don't believe you should donate blood with MGUS or any blood related condition. Have you heard otherwise?

Althought this is a site based in the United Kingdom, my bet it is the same here in the United States: https://www.transfusionguidelines.org/dsg/wb/guidelines/ha001-haematological-disease#:~:text=Must%20not%20donate%20if%3A,of%20unknown%20significance%20(MGUS).
Ginger

Jump to this post

@gingererw @dianegrant

I was diagnosed with MGUS last August 2022. I was a regular blood donor - over 5 gallons so far.

At my first appointment at MD Anderson - Houston - I asked my Myeloma Dr. about continuing to donate blood. He said no. That was that !

Luckily my husband continues to donate every 2 months and is a "Brothers in Arms" donor.

REPLY
Please sign in or register to post a reply.