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» LymeNet Flash » Questions and Discussion » Off Topic » Should I tell blood bank about LD? WWYD?

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Author Topic: Should I tell blood bank about LD? WWYD?
DallasGal30
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I have been diagnosed with chronic Lyme in the past
year.

I had donated blood about 5 years ago.

Now, since I don't know when I contracted Lyme, should I contact blood center and let them know?

I feel a moral obligation to do so. And, I'm very sure I will get a big, blank stare when they hear "chronic Lyme". WWYD?

Posts: 27 | From Dallas. TX | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
Geneal
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I doubt they could trace your blood back that far.

I realize you feel an obligation to alert someone, but

I am not sure they even keep tabs of that info that way.

Best thing to do is not donate again.

You did not knowingly share your disease with someone else.

In La. now, one of the questions prior to blood donation is have you ever been dx. with Lyme disease.

I would maybe send a letter telling the blood bank why it is important to include

Lyme disease as a contractable disease and tell them why it is important to refuse

Any blood from anyone who has ever been diagnosed (or received the Lymerix vaccine) [Smile] .

Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
treepatrol
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I would tellem and never give blood again. I know I wont or donate organs.

--------------------
Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

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Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
HaplyCarlessdave
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quote:
Originally posted by DallasGal30:
I had donated blood about 5 years ago.

Now, since I don't know when I contracted Lyme, should I contact blood center and let them know?

I am quite sure (though not totally) that at this point, after 5 years, it is way too late! But I would definitely avoid giving any more blood- at least until I was absolutely sure there was no active disease in there, and possibly for good. Actually, they wouldnt let me give blood, on account of having had babesia, though it would seem that lyme ought to be even more of a concern.
DaveS

PS- excuse the lack of apostrophys (oops-accidently typed one there); a (very) minor bug has surfaced)( but I also cannot move cursor backward....- oh,now its (oops aggain) okay..- its (ha!- didnt get me there (or there))) only after you TRY to type an apostrophy that you cant move trhe cursor backwards...)

Posts: 4567 | From ithaca, NY, usa | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
Cobweb
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I told them and they didn't take my blood.


I felt like an outcast-but i still got a t-shirt.

Now I just help out with registration and getting drinks for people and holding hands.

So I still contribute-I just don't give blood.

Take Care,
Carol

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Itsy_bitsyone
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I used to be a registered organ doaner before I knew what was wrong with me.

I had never given blood and now I know not to ever give blood. Not because I didn't CARE...but because I have never weighed enough...other than when I was pregnant...since I have been an adult.

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HaplyCarlessdave
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Oh, I see I replied already. But, hopefully if someone was given your blood, either
1) they were on antibiotics already, so that the lyme wouldn't have a chance to get into their blood cells before being lethally exposed,
2) the blood was actually taken before you had lyme, or
3) it was given to one of the, um, ....'researchers'... who is being paid to ...'prove'.... chronic lyme doesn't exist...

DaveS

Posts: 4567 | From ithaca, NY, usa | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
Tracy9
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My son donated last week at his school. He has chronic lyme. I called the school to notify them and they just said, "we just host it; someone else comes in and does it." I couldnt' find out who hosted the drive, and the school was no help.

So someone may get his blood. Get this: I live in Connecticut, and they DO NOT EVEN ASK.

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NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
randibear
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my husband has been exposed to hepatitis in vietnam apparently and i've got lyme. carter blood bank said no to both of us.

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
   

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