I really dont know. She told me that the daughter had significant pain with the change. More the blood type change than the transplant itself.
She never really recovered and is extremely disabled.
She sounds similar to what I’ve been thru.
Let her know to come join our page . We are a great group who support each other. No one really understands the physical/psychological aftermath . I’ll send it to you in DM. Those who use their own cells bounce back much better. The effects from the intense chemo and the restrictions to avoid gvhd is life changing.
Just recently (October) I forced myself to get a 16 hr/week job.(4 days 4 hours) to make myself get out of the house. I was heading down a bad road over the years letting the pain dictate my life. I do need medication to tolerate it, but it’s been life changing to get this lil part time job.