Bk virus again. : Hey everyone, hope you... - Kidney Transplant

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Bk virus again.

Rmatthew profile image
7 Replies

Hey everyone, hope you’re all doing well.

Before i posted on this page about having the bk virus, my creatinine is still high because of it, but the virus came down the last 2 weeks. They said about holding off on giving me medication for the virus because it was stable at the moment. I was wondering that if anyone had started the medication they’re talking about and what were the side affects of them? In case I do need to go on them myself,

Thanks!

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Rmatthew profile image
Rmatthew
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7 Replies
Cazzy41 profile image
Cazzy41

I have had the BK virus for over a year now, the only thing that has been done for me is stop the Cellcept and put a 5mg prednisone in with my Tacrolimus 3mg. I have never been ill with the virus it’s just there and playing around with my blood results. I was told a couple of weeks ago that I should come to terms with the fact I may never get rid of it unless the kidney fails and I’m back in dialysis!! Not exactly what anyone wants to hear to be fair. I am 3 years post transplant today!! And it’s not been easy but it’s better than the alternative. Good luck and please keep us updated xxx

Drdetroit profile image
Drdetroit

I am 9 yrs post transplant. I had 3 rejections in the first 2 yrs. after massive steroids I was ok for 4 yrs, then my creatnine started bouncing around. After another biopsy showed BK, my prograf was reduced & cellcept eliminated for a while. BK is now gone, I do blood work monthly & I take 1mg prograf 2x daily & 500 mg Cellcpt 2x daily. I never had BK, but my donor did. Before Bk, my creatnine was 1.4 & after the biopsy was 2.9. it is now steady for 2 yrs at 2.5

Drdetroit profile image
Drdetroit

If the meds they want to give you are IV steroids, if you are diabetic they will make your blood sugar go crazy & make you very hungry. Also some insomnia

Charly1429 profile image
Charly1429

I’m, 8 months post kidney transplant, I’ve had mild Bk Virus now it’s out of my blood, but one Nephrologist said it always stays in your urine? Also, never had issues while I was on BK.

KidneyBham profile image
KidneyBham

I am 2 1/2 years out, I got the BK virus 6 months after transplant, I was also taken off cellcept and put on 20 mg of prednisone for 2 months than tapered off to 10 mg along with tacrolimus 4 mg x2 a day. The Bk virus is finally almost out of my body, I had no problems with it and my numbers got up into the millions, I’m less then 3k now. I pray you have a positive outcome and there are no kidney rejections in Jesus name.

mtwskk profile image
mtwskk

Bk is not something you do wrong, it's something that your donor had and is controlled by decreasing your your tag/program. I'm 9 years out and have had it twice. You just need to get the bk virus tested if you are susceptible to the virus. The test tell all. I didn't get tested one year and my Creatine went up to like 2.3 from my baseline of 1.8 quickly. They thought the kidney was rejecting put me in the list for a new one. They we found the bk. It took about 4?months to get the counts back in line and I think they did a couple of pred spikes. But they got rid of it. It's now 3 years later I test one a year or if my Creatine spikes. Good luck it's not a bad thing just something you need to be aware of. There is one other virus like this but I don't get that one so I forget the name it's something like cv.

Rmatthew profile image
Rmatthew in reply tomtwskk

Hi, my doctor said that I most likely had the bk virus when I was on dialysis but was being controlled by my immune system, and then when I got the kidney it was kinda reactivated and that’s what’s made my creatinine go up, and that they had me on too high immunosuppressants

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