← Return to MDS (myelodysplastic syndrome): When to start treatment?

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@alive

My transplant for AML was 8.5 years ago. My transplant was the miracle I was praying for. I was only a few days from dying when I was diagnosed. Getting a transplant is a personal decision and there is a risk of complications and dying. However, there is also a chance for a cure.

When I was preparing for my transplant, I read all about the statistics. For me, it was I was either going to live or die. I took the chance and proceeded to get a transplant. I have no regrets!

I recommend that your husband shares his hesitations with his doctor and the social worker on the transplant team. It will be also helpful to talk to the transplant recipients and hear about their experiences.

Wishing your husband and you all the best as you make that difficult decision!

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Replies to "My transplant for AML was 8.5 years ago. My transplant was the miracle I was praying..."

So thankful you've gained a second lease on life! I'm sure it was a scary and difficult choice. Sounds like it was your last chance and you took it! Hope your life is now full of happiness and that you're making all your dreams come true! Thank you for sharing. 😊

Thank you. He needs to decide if he wants to continue what treatment he is on, which seems like it may be forever, or take the risk of BMT. It’s hard to see him suffering so.