Dental implant with MPN

[LucyAshtonGeering]

Hello,

Have you had a dental implant since being dx with Myelofibrosis, and if so which material is your implant made from?

I’m trying to decide whether to have ceramic or titanium, and am seeking any experiences with such by MF patients.

Thank you,

Lucy

[2003UK]

Hi Lucy, I don't know if this is any help at all. I have had CLL for 17 yrs with a compromised immune system and about 15 yrs ago I had to have extensive dental work done due to re-occurring infectionsAnd I was advised against anything invasive i.e. implants and ended up with 2 dentures, now I am sure things have changed over the year, but I thought I would let you know my experiences for what it's worth. Look after yourself and I hope your dental work is sorted soon.