← Return to Kidney disease: Figuring out minimal change disease (MCD)

Discussion
Comment receiving replies
@rkndvm

I have not scheduled an initial visit yet, but will let you know what I find out.
I never sleep more than a few hours at a time. 🙄 Insomnia is my worst side effect! I “rest my eyes” tossing and turning and take naps. So grateful to be retired.

Jump to this post


Replies to "I have not scheduled an initial visit yet, but will let you know what I find..."

I rarely sleep. Didn’t know if this is a side effect. I am currently taking Tacrolimus 3mg every 12/hrs. Didn’t know if insomnia is related to the medication or the MCD. I pray that your visit goes well.