I’ve joined two Facebook groups that are really helpful. Sometimes I have a question, and I hear back from so many people who can answer from experience. Then other times, I get to be the ‘expert.’
Intended for US residents only Intended for US residents only
Intended for US residents only
Answers and support for where you are in your transplant journey
It’s hard to tell who will develop graft-versus-host disease (GVHD) after a stem cell transplant, or how serious it might become. There’s no one way in which GVHD affects all patients who get it. There’s no one place in the body it can strike.
That’s why it’s important to know what to watch for and act quickly if you notice any new or changing GVHD symptoms.
This site can help you understand the two types of GVHD—acute and chronic. Whether you’re a patient or caregiver just learning about GVHD or deep into your journey with it, you’ll find information and an array of resources to help support you.
Get support along the way
Register for resources
Sign up for occasional email updates and to receive your GVHD introduction kit, including a personalized GVHD Medical Alert card you can share with others who need to understand your health status.
Share your story
Join our GVHDspeaks program and use your experiences to support others living with GVHD.
Where are you on your transplant journey?
Click to see what steps you can take along the way to help with GVHD.
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Pre-transplant
What happens before stem cell transplant?
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During the hospital stay
What happens after the transplant?
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Transitioning to home
What to expect after discharge
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First year after transplant
What should I be aware of?
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More than one year after transplant
What to keep in mind
Pre-transplant
What happens before stem cell transplant?
During the hospital stay
What happens after the transplant?
Transitioning to home
What to expect after discharge
First year after transplant
What should I be aware of?
More than one year after transplant
What to keep in mind
Connect with others who’ve been there
Find online groups, support meetings, one-on-one mentor services, and other opportunities to talk with people like you dealing with GVHD.
I’ve joined two Facebook groups that are really helpful. Sometimes I have a question, and I hear back from so many people who can answer from experience. Then other times, I get to be the ‘expert.’Barbara A.
2013 transplant recipient
Talking to other patients has been more enlightening to me than anything, and they’ve also appreciated me sharing my story.
Benton B.
2018 transplant recipient
Note: Healthcare Professionals are the best source of medical information.