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Author Topic: finding out your anti-body's  (Read 2704 times)
marlinfshr
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« on: September 18, 2014, 04:01:55 PM »

I keep reading posts where people know their antigens, antibody's or whatever and where they stand as far as possibility of getting perfect match. Not worried about placement on the list as I understand that comes with time and a perfect match will go to a newly listed candidate over one who has been listed for years if it's not perfect for him.

I have been active only since January of this year so I still have plenty of time. I do remember them saying at my initial evaluation last year that there is about a 3 to 5 year wait for my blood type.

My question is how do I get that info? All I ever get is a letter from them monthly or by-monthly which reminds me to have my clinic send my monthly blood draws to the transplant and states that my status is active. I guess I should call and ask as perhaps this hospital doesn't automatically send out that info.

I called after I had the bypass to let them know and gave them my info of where it was done so they could get the records. I thought I would receive an update putting me on hold until a stress test or something but I did receive another blood test reminder today with current status active.
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iolaire
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« Reply #1 on: September 18, 2014, 07:09:16 PM »

All I ever get is a letter from them monthly or by-monthly which reminds me to have my clinic send my monthly blood draws to the transplant and states that my status is active.
I'd love to get that frequent of info to confirm that I'm still active. 

I got a letter to say I was listed and talk about the labwork three years ago.  Then after that the lab boxes and tubes each quarter and a reminder if I'm late but otherwise nothing.   So now three years later I get a letter from my insurance co re authorizing a transplant for three years!  Luckly since last nov. I've started to get some calls, so they talk to me a tad about my status, and I know that I've moved from about number six to number three or so.  For the longest time there was some worry about if I was active and they had me in the right status, it would have been nice to get a periodic letter.

So to answer your question I don't know my antibodies, but I am told the level of my alternate staus when they call.  In three and a half years they have not asked for any additional tests.
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Transplant July 2017 from out of state deceased donor, waited three weeks the creatine to fall into expected range, dialysis December 2013 - July 2017.

Well on dialysis I traveled a lot and posted about international trips in the Dialysis: Traveling Tips and Stories section.
rocker
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« Reply #2 on: September 18, 2014, 07:19:09 PM »

We've always had to ask.
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Angiepkd
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« Reply #3 on: September 18, 2014, 07:29:01 PM »

I asked specifically what my antibodies were during my pre-transplant testing.  I got a kind of vague answer like 3-5%.  My coordinator acted like it was odd for me to ask.  She said if they were high enough to be a problem, I would be told.  So, in my experience, if they haven't mentioned it, then it probably isn't an issue.  After my transplant, I was put in the moderate rejection risk category because my husband was my donor, and we have children together.  They worry that I could have developed antibodies to his DNA during pregnancy.  I have to admit the whole antibody thing is still a little confusing for me.  Call and talk to your transplant coordinator.  They should be able to tell you.  Best of luck to you!  Hope you get the call soon!
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PKD diagnosis at 17
Cancer May 2011, surgery and no further treatment but placed on 2 year wait for transplant
October 2011 first fistula in left wrist
April 2012 second fistula in upper arm, disconnect of wrist
January 2013, stage 5 ESRD
March 2013 training with NxStage home hemo
April 2013 at home with NxStage
April 2013 fistula revision to reduce flow
May 2013 advised to have double nephrectomy, liver cyst ablation and hernia repair. Awaiting insurance approval to begin transplant testing. Surgery in June.
June 2013 bilateral nephrectomy.
August 2013 finishing testing for transplant, 4 potential donors being tissue typed.
January 2014 husband approved to donate kidney for me
March 4th 2014 received transplant from awesome hubby. Named the new bean FK (fat kidney) lol!  So far we are doing great!
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