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| | |-+  Anyone experience pain at transplant site and beyond?
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Author Topic: Anyone experience pain at transplant site and beyond?  (Read 25548 times)
olivia
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« Reply #25 on: August 28, 2011, 11:46:04 AM »

I got it at a nutritional store. I wanted the natural pure ginger. It is " Reed's Crystallized Ginger" , baby ginger root sweetened with raw cane sugar. It tastes sweet on the outside, chewy, once you start chewing it tastes like ginger, Then it bites, a little hot like those red hot candies. I was taken back with the "hot" bite at first, getting used to it.   It is helping, so I am going to continue to take it when the pain gets bad.
It is an anti  inflammatory, and also thins blood so I don't want to take it everyday, only when I need it. It makes me belch a bit too.
Doc said  pure ginger tea also, but I tried that before and that taste like dirt to me, yuck.

Olive :flower;
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SooMK
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« Reply #26 on: January 01, 2016, 06:28:41 PM »

Another oldie but goodie thread. It came up via a Google search--all kidney roads lead to IHD, ha! Might have overdone it this weekend with my three year old granddaughter. The family was joking it's really my playtime. Didn't even get home before I was having sharp pains along my incision. I've had them before but never so severe as tonight but I feel fine except for that. Also interested that someone has joint pain because I get that a lot. I feel better just knowing someone else has the same pains I do! Felt kind of sad reading posts from people who haven't been on IHD in quite awhile. Happy New Year everyone.
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
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