[maryotaber]

Hello everyone!

I've been a lurker here for 4+ years now when I was diagnosed with SAA in my junior year of college and can not thank you all enough for all the information/perspective I've gotten from reading everyone's posts. I had my BMT at Dana-Farber this past March and am so happy to have gotten to Day 100 so successfully (helloo salads!). I had my second Hickman removed last week and if my magnesium level would finally come up I'd feel like a new woman!

Anyone else have a hard time getting their Mg level to come up post trasplant? I've also developed horrible tinnitus in my right ear, which after having a bunch of tests done, seeing an ENT & neurologist, and trying zillions of meds, I'm just hoping it's either meds-related or random and will go away with time. But if on the off chance anyone else has experienced this, I'd love to hear stories!

Many thanks and well wishes to all!