
Last Friday during labs they ordered a couple of tests to check what percentage of my cells were my cells and what were the donor cells. There are 2 tests one for t-cells (immune system) and a different one to check the platelets, white blood cells and red blood cells. 100% of my blood cells (platelets, WBC, and RBC) are donor cells. It can't get any better then that. 90% of my T-cells are donor cells and 10% are mine. This is to be expected since I am on immuno-suppressant drugs. When they wean me off those it will go to 100% donor cells.
So this is good stuff. Day + 38 and donor cells are doing their job.
In other news... I had been having to go in for almost daily infusions of Magnesium. The tachrolimis causes me to lose Magnesium. This would take anywhere from 1-4 hours and kept me tethered to the hospital. On Saturday we started "home" infusions. I get shipped a bottle of magnesium and saline, and can infuse myself each day. It is very easy. And the best part is no more hospital. I have transferred back to the clinic and only go twice a week now. Mondays and Thursdays.
Only down side is I seem to be a little sensitive to IV magnesium. I bothers my stomach a bit... but heats me up (fells like I am cooking from the inside out) and causes sore muscles or discomfort I have to be a bit more significant. We're experimenting with when to do the infusions to avoid this. I am thinking we'll probably start doing them at bed time. Hopefully I can just sleep through it.
We'll see. The magnesium is the only major complication I have at this time and it really is minor compared to what others are going through. I credit all the prayers and good vibes for how I am doing so far. It's all been good news...
The kids will be up this weekend again!
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