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» LymeNet Flash » Questions and Discussion » Medical Questions » What about those who do give blood????

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Author Topic: What about those who do give blood????
Kerryblue
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Last night woke in middle of night. Where the heck this came from all of sudden.

I know people have mentioned here they would not give blood. Nor I.

Yrs. back Before my dx. I had gut feeling I should not give blood becuase knew something was wrong with me physically.

I imagine they do not send or check for lyme upon donated blood.

All those people unknowingly infected.

Should the govt. be sued or held liable since people have been fighting for yrs. to get lyme acknowledged & fight for correct testing. Including CDC now admitting they could be doing better testing.

Many like myself go for yrs. not knowing they have lyme. I know of people, such as my daughter who I am suspicious of lyme.

They have given blood many times.

How awful to think you are getting well tested clean blood. Injected such a serious life altering & threatenting disease. So many like myself left untreated. Or have no idea what is wrong with them.What is your take on this, maybe used to help our cause to get proper testing & treatment.???

Is this not a crime, when people high up know of the lyme growth & somewhat epidemic. More than other stuff that gets alot more press.


Posts: 746 | From Clearwater/fl/Pinellas | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
treepatrol
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Giving blood big no no if you have lyme .
I had a freind who has been bittin and told he didnt have lyme and later bittin again and had the bullseye rash I told him if I had a rash I would never donate again untill they come up with a good sreening procedure. I think this is how a lot of it is being passed around and suddenly becomes MS ALS Lupus etc.

Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
Rita
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About a year? ago there was a blip on the news about a person who got MS from an organ transplant. You'd think someone would have gotten a clue from that but, as far as I know, nada.

The Red Cross accepts blood from Fibromyalgia patients. All of this will turn out to be a major national catastrophe, especially when the govt, already with a potentially ruinous national debt, has to pay for it.


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Corinne E
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Hi Rita and all,

If one has fibro, one cannot give blood. I gave blood for years, then about 4 years ago I mentioned I had fibro, was that ok? The person said absolutely not, I asked why not, she said they were told that it could be passed on to other people. Isn't that a dandy! I am going to try to give blood again, only this time will say lyme and see what she says. If she says ok for lyme, then I am really going to make a fuss.

I have even taken myself off the organ donor program.

Take care

Corinne


Posts: 461 | From Abbotsford, BC, Canada | Registered: Oct 2003  |  IP: Logged | Report this post to a Moderator
Kara Tyson
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There is a good book called, What The Gov. Isnt Telling You About AIDS. It is written by an orthopedic surgeon in San Francisco. She got in serious trouble with the hospital she worked for because she went head to head against the Red Cross who despite knowing HIV was in blood continued not to test and to have blood drive in predominatly gay areas of the city.
Posts: 6022 | From Mobile, AL | Registered: Apr 2001  |  IP: Logged | Report this post to a Moderator
Rita
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I'm glad the Red Cross has changed it's position about Fibromyalgia. I gave about a gallon and a half, over the years, and told them, every time, that I had Fibromyalgia. I stopped giving, in '89, when I became Lyme Literate.

The Red Cross position on not testing blood for AIDS, years ago, is resposible for decimating the Hemopheliac population. At the time, they used blood products in their treatment and much of that product was contaminated with AIDS.


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breathwork
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The last time that I went with someone to give blood, they did not allow lyme patients to give for five years after being symptom free...this was a few months ago.

Also, we would not be allowed given all the medications that we take...

For those who have lyme and don't know it, there's nothing to be done until the blood supply is tested for it....and even then, given the inaccuracy of testing today, that would be a shot in the dark.


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Nancy-OH
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A couple years ago I went with my daughter who was giving blood for the first time.

(I no longer give.)

However, I asked out of curiousity what the Red Cross policy was with regard to Lyme.

The nurse had to look it up and then told me a person had to be on abx for one year before giving blood!

I was floored! I hope they've wised up since a couple years ago!


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Kara Tyson
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I never thought much of the Red Cross anyways. My grandfather (a WWII vet) hated them with a passion--ask any WWII vet. A very very low opinion!

It never suprised me when they raised money after 9/11 and the families never got the money.

During WWII they would raise money "for the GI's". Then they would serve coffee to the GI's and make them pay huge amounts for a lousy cup of coffee. Care packages were often paid for as well (after they items were donated by the American public).

Any thing for a buck, I guess.


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greg
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Not to add a sad twist to this or anything. But my grandfather fell and broke his hip a month ago. After the surgery (joint replacement) he was given a blood transfusion, to push the pain medication out of his body.two days later he died. He was 84, but not in bad shape. You never know what you are getting, with someone elses blood. God only knows how long I had lyme before i was diagnosed, or even knew what lyme was. The good thing was I stopped donating after i went to 3rd world countries with the service.

no the government wont take the hit for this, you can bet that.


greg


Posts: 740 | From frederick,md,usa | Registered: Jun 2001  |  IP: Logged | Report this post to a Moderator
Melanie Reber
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For your information:

Thinking of being a Blood or Organ Donor: http://flash.lymenet.org/ubb/Forum1/HTML/021835.html

------------------
C O L O R A D O * S U P P O R T * S Y S T E M
[email protected]


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Kerryblue
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I took my name off of the list as doner for organs or blood. Soon as I started feeling sick on regular basis even before dx of fm/ebv/lyme/me/mps/.

It was a gut thing, I asked my daughter not to give blood, & she doe`s since I suspect her having fm or lyme.

I have to admit after being so sick for so long would have to think hard & long if I would w3ant myself to accept this blood under an circumtances.

Would not wish this life on anyone. Well maybe a duck or 2 or someone else who stalked me.

I was being sorta sarcastic about the govt. being sued. I know that would prob. never happen.

Just all the cover-ups. After working with clinic & Bowen study. It just seems tragic that some are giving blood who could be just passing this dang stuff to another human due to them not testing properly when they could.

I also had bad experience with Red Cross back during Nam times.

Like to hear any other thoughts. Thanks for yours...


Posts: 746 | From Clearwater/fl/Pinellas | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
StrengthToStrength
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Since we all have been cured with 3 weeks of antibiotics, and just have "post-Lyme syndrome", there should be no problems with us being blood donors.
Posts: 236 | From D.C. | Registered: Mar 2003  |  IP: Logged | Report this post to a Moderator
   

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