Re: New to the Group

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Re: New to the Group

Curtis R Anderson

19 Jul 2006 01:37

>>Surely there are plenty of fellow sufferers out there who would like to
>>share heir problems and, perhaps, a chuckle or two about it all.
>>Hugs for Everyone Concerned
>
> No this isn't alt.support.probate.
> I don't normally mention typos but this one was to good to pass up.

Yup. We were dying to hear that one.

Anyway, with the heat and sun, Marie is hanging on these days. I'll have
to ask her to tell you what happened Sunday.

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Curtis R. Anderson, Co-creator of "Gleepy the Hen", still
"In Heaven there is no beer / That's why we drink it here ..."
http://www.gleepy.net/ ICQ: 50137888
mailto:gleepy@gleepy.net (and others) Yahoo!: gleepythehen

Timothy Luders	18 Jul 2006 02:02
> Surely there are plenty of fellow sufferers out there who would like to > share heir problems and, perhaps, a chuckle or two about it all. > Hugs for Everyone Concerned No this isn't alt.support.probate. I don't normally mention typos but this one was to good to pass up. Timothy

Diane

17 Jul 2006 14:34

I was diagnosed with Lup[us in 1993 I had always been a very active
person.. Classical Ballet, Swimming competively, Horse Riding and
Yachting.I was a very happy person with loads of self-confidence.
In about 1998, I started to get aches and pains in all my joints and
muscles along with constant fatigue My husband eventually left me for
some one youngerr I started to feels as though I was a hyphchondiac! At
last one lady suggested I go to see and Immunoligist and after a few
Blood Tests , I found that I had, at last a name to put on why I was
feeling likeI was. Mind you, ignorance is bliss. I had no idea what was
to come!
I have had 4 joint replacements, 2 fused joints and a Laminectimy and
Disctectomy.I have lost the vision in my left eye and because it
continued to be painful, had to have the whole eye removed and I now
wear a Prostheseis. This hasn't done much for my self-esteem which was
pretty low anyway. None of my family or friends seem to understand my
spcecial needs and, I think, I use the name "lupus" to get of attending
vareious functions.
I have given them all "pamphlets" to read but they don't seem to be
very interested in reading them!
I know, quite well, that I sound as though I am whingeing. That is why
I thought a support programme like this may be of some help to me. I am
not unhappy all the time and it would be quite fun to share the
"miseries" of this affliction and to have a laugh about it. After all,
there are many times when I think to myself, "This would be funny, if I
didn't feel so alone."
Surely there are plenty of fellow sufferers out there who would like to
share heir problems and, perhaps, a chuckle or two about it all.
Hugs for Everyone Concerned
Diane
rwh81505@bigpond.net.au

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