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Medical Forum / Diseases and Disorders / Cancer / February 2006

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I donated blood to a Leukemia patient

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w b evans - 12 Feb 2006 23:14 GMT
A few years back I donated blood to a co-worker's cousin who had Leukemia.
Don't know what kind.  But it was in the last stages for her.  A few months
later I asked him about his Cousin, and he said that it was a miricle that
the doctors couldn't explain. She was cured, and back in life.
I've never had even a cold in the last 20 or 25 years.   Maybe I've got good
antibodies or something.  I like to call it "Walter's magic blood".
I'd like to say that is was my blood, but I was one of seven doners to give
for her.
Whenever I bring it up to my family Doctor, she just smiles.

If anyone knows of someone who has Leukemia, and needs a blood doner, let me
know.  No strings.
I'm just a blue collar worker from Northern N.J.

walt evans

J - 13 Feb 2006 01:16 GMT
> A few years back I donated blood to a co-worker's cousin who had Leukemia.
> Don't know what kind.  But it was in the last stages for her.  A few months
[quoted text clipped - 11 lines]
>
> walt evans

Well done, walt !
Giving blood is fairly simple, but not enough people do it, IMO

How about bone marrrow or stem cell?
We get posts about those, from time to time.
You would have to be "typed" (I think).
Here's the most recent  http://tinyurl.com/d2kf5
Click the blue line under his email address, type in the code and his email will
be revealed.
It's more complicated and maybe expensive and I think your donation goes through
a central place for the US and one for Canada (ie you can't pick who you donate
to), but to or in Poland I don't know. Then there's shipping, storage and
customs (of flying there), but if you're ever interested,
http://www.cancerbacup.org.uk/Treatments/Stemcellbonemarrowtransplants/Generalin
formation


and http://www.acor.org/mailing.html?l=b BMT-talk list

There's also leukemia lists there under A, under C and under P
Click to "join", select digest mode to receive.
J
w b evans - 13 Feb 2006 19:42 GMT
J,
Yeah, years ago I registered for the Bone Marrow Registry.

Thanks for the links, I'll check them out.

walt

Signature

walt evans
NX140DL

>
>> A few years back I donated blood to a co-worker's cousin who had
[quoted text clipped - 42 lines]
> Click to "join", select digest mode to receive.
> J
alex - 13 Feb 2006 21:06 GMT
> Yeah, years ago I registered for the Bone Marrow Registry.
>
> Thanks for the links, I'll check them out.
>
> walt

You probably are still in the registry good matches are difficult to find if
you are no related. I think you did a great thing with your domination, and
hopefully you'll match again and that person will become lucky too. Alex
J - 14 Feb 2006 19:40 GMT
> Yeah, years ago I registered for the Bone Marrow Registry.

Good for you, Walt and God bless you.

And by the way, please forgive alex.
English is her second language and if anyone here is into domination, I exepct they discuss
that on a bondage newsgroup, not here  hehe..

Best wishes to you in your helpful endeavours.
J
patrz - 15 Feb 2006 22:10 GMT
>> Yeah, years ago I registered for the Bone Marrow Registry.
>
[quoted text clipped - 7 lines]
> Best wishes to you in your helpful endeavours.
> J

I just cannot understand why you take every opportunity to be catty to Alex.
It certainly shows your claws and it's very childish.  Are you jealous of
her knowledge of medicine?

I can understand some people appreciating your help in regards to searching
on the net, but I really question anyone's praise of your advice.  I think
you go way beyond you knowledge of medicine and offer your advice too
readily.  MMHO

patrz
figgertoes - 16 Feb 2006 21:35 GMT
> I can understand some people appreciating your help in regards to searching
> on the net, but I really question anyone's praise of your advice.

Then you'll have a lot of questions for a lot of people.  Yes, J is a
skilled researcher, but she is so much more to many of us.  I don't see
anyone else stepping up to the plate to do all she does.

>I think  you go way beyond you knowledge of medicine and offer your advice too
> readily.

Maybe you haven't been around long enough to observe how this group
functions.  J does much if not most of the legwork - researching
outside sources & gathering needed info from posters.  Then she often
calls for advice, comments, confirmation from  seasoned medical
professionals & from others who are traveling or have traveled a
similar route.  A lot of cross-checking takes place.  Note the clifto,
chris ness, chy & araik sub-support system that J played a big part in
pulling together.  Lots of teamwork. Lots of support.

If  she posts anything in error (rare) , the experts correct her & she
readily admits her mistake.  More often, the experts confirm her
research & maybe add to it.  She empowers us to be partners in our own
or a loved one's care by supplying the information we need at the time
we need it.  She is not off on a tangent of her own.  I am personally
very grateful for the loving support she provided Socks & me.

Her work allows Steph & others to work efficiently.  J knows what
information they need & organizes it for them, so they can pop in &
provide medical information efficiently.

That's what I'm seeing...
People do have options & can choose to go it alone or get their
information from other sources.  Or to take what they need & leave the
rest.  We come here; nobody goes out chasing us down.

> MMHO

Is this an acronym, please?  I don't know this one...

My apologies, J, if  any of this is inaccurate.  Just my point of view.

Figgertoes
J - 17 Feb 2006 10:24 GMT
> <thanks - an explanation would be longer than the FAQ>
> That's what I'm seeing...
> People do have options & can choose to go it alone or get their
> information from other sources.  Or to take what they need & leave the
> rest.  We come here; nobody goes out chasing us down.

Well, actually, I browse through other newsgroups, and sometimes I do refer people
here <g> or even just recently I replied to someone here and he was seen then, on
another newsgroup, essentially reasking the same question and I crossposted back to
sci.med.diseases.cancer to give either of the oncologists, reading there, the
chance to correct me (what I told him) and none did.  If I see a cancer question,
on another newsgroup, I reply to them and/or refer them here. Some would rather
stay on their "home" newsgroups, with their existing support system. I don't go
searching them out (via the archives). It's just if I notice one, on other
newsgroups that I browse through.

The longer story is she and I have disagreed for years, about certain issues (maybe
back 6 - 8 years).
I was posting more (than now) to the breast cancer newsgroup and backed off when
challenged by her, for the sake of the others on that newsgroup.  And especially
since the big fight a year or so ago. She's been critiquing me for years and I've
stopped almost everything that she's found fault with, she just finds something new
to critique. So since I've stopped (decreased my posts to the breast cancer
newsgroup), she's been targeting me here..

So if he thinks my claws are bad, he'd best look at the bigger picture and
understand the point of some of her posts. He may have tunnel vision or miss some
posts. What I've noticed, in the past year, since the big fight on this newsgroup,
is she'll often skip over posts on the breast cancer newsgroup and come directly
here and post one helpful post, then aim a criticism at me.  I've watched that
daily for almost a year.  I've turned the other cheek (ignored it), bitten my
tongue, for the sake of this newsgroup (and everyone here, including me).

As best I can recall and my memory's not perfect, I've critiqued for posting the
wrong name (non-existant) of a breast cancer medicine. I waited a few days for her
to correct it. When she didn't, I pointed it out to her and her reply was not "I
apologize, I meant to say XXXX". The reply was "any professional would have known
what I meant" (another barb at me). Well, I've got news for her. There may be
professionals who read this newsgroup, but most of the readers are probably not.
Leaving such misinformation uncorrected, leaves people reading through Google, to
go off asking their oncs about a non-existent breast cancer medicine. Leaves them
searching the www for said medicine, when it was an error that she could have and
should have corrected.

Then there was this one that should bave been "donation". To the best of my memory
those are the two main "problems" that I've created with her for the past year. To
be honest, I was upset about the insensitive way that she responded to Em. Em
wasn't feeling well and she'd just found out that her mother has a recurrence.

Other comments: Tim (who is, in some ways, the equivalent of me here) has never
told me to get off the breast cancer newsgroup. If he had problems with me, he has
my email address and could have told me.

Yes, I correct my posts where I feel something I posted was incorrect or
misleading. And yes, I apologize for errors. I'm not apologizing to her because
I've never seen her apologize for anything. Not her errors, not her conduct.

Yes, Steph or Peter or sometimes madiba correct me or add to what I've posted.
Steph and Peter have my email address. If either of the 3 (Tim, Steph or Peter)
felt it's better for the newsgroup for me to be off here, I welcome their telling
me so, on newsgroup or by email.
I sure wouldn't argue that point with them, if they wanted me off here.

So anyway, this newsgroup is not about me, nor Alex.
I'd like to get back to what I feel I do best, supporting, information, replies,
caring.
I hope we can write this one off to the poster not knowing all I do and not seeing
the big picture (of my various cancer related efforts and what has transpired in
the past, on both newsgroups).
That's my recollection and point of view

> > MMHO
>
> Is this an acronym, please?  I don't know this one...
>
> My apologies, J, if  any of this is inaccurate.  Just my point of view.

MHO means "my humble opinion". I don't know what the other "M" means and I'm into
searching it.
IMHO means "in my humble opinion", so it's some variant along that line.
Hugs
J
J - 17 Feb 2006 10:30 GMT
> > > MMHO
> >
[quoted text clipped - 4 lines]
> MHO means "my humble opinion". I don't know what the other "M" means and I'm into
> searching it.

That should have read "I'm not into searching it". <g>
You could though by typing it into Google.
J

> IMHO means "in my humble opinion", so it's some variant along that line.
> Hugs
> J
Figgertoes - 17 Feb 2006 14:59 GMT
>> > > MMHO
>> >
[quoted text clipped - 13 lines]
>> line. Hugs
>> J

I had typed it into the acronym translator website:

http://www.acronymfinder.com/

with nil results before asking here.

Thanks for giving me the drift of it, J.
Fig
J - 17 Feb 2006 21:14 GMT
> J <studras@anon.inv> wrote in news:
>
[quoted text clipped - 12 lines]
>
> with nil results before asking here.

Hello oh wise one.
I apologize. I should have known that you would check first.
I also tried searching (various ways) and couldn't find.
And so that's all I can do, but at least we have the gist of it, eh?
Hugs
J
w b evans - 17 Feb 2006 23:14 GMT
Sorry I brought the whole string up.
walt evans

Signature

walt evans
NX140DL

>A few years back I donated blood to a co-worker's cousin who had Leukemia.
>Don't know what kind.  But it was in the last stages for her.  A few months
[quoted text clipped - 11 lines]
>
> walt evans
J - 17 Feb 2006 23:56 GMT
> Sorry I brought the whole string up.
> walt evans

Don't worry about it walt.
Feel good about what you're doing.

What happens here is mild compared to what was happening up until a few years
ago and what I see happening on other newsgroups; cursing, swearing, name
calling and other hurtful things.
People disagree, but we're pretty tame compared to other newsgroups.
So feel good about what you're doing and have shared with us. :)
J
 
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