Question:
Joanne, Is it possible to get a "digest" version of this. My inbox is kind of overflowing from the rest of the stuff I get now. Thanks, Jackie "Joanne" <joa…@frsw.freeserve.co.uk> wrote in message
news:38c55708.9006365@news.freeserve.net… – Hide quoted text — Show quoted text -> Hi > This is just to let people know about our lupus email group. We have > over 70 members from all over the world, all who have lupus, or are > families of lupus patients. > People can get support, advice, make new friends, through the group. > It does generate a lot of emails every day, so be warned 
> You can join the group by sending an email to > uklupus-subscr…@listbot.com > or you can join through my website at www.uklupus.co.uk > We also have a lupus chat email group that is just for sharing poems, > jokes, stories, general chit-chat etc. > To join send email to lupuschat-subscr…@listbot.com > or through the site as before. > Joanne > www.uklupus.co.uk
Response:
No, sorry. Joanne On Sat, 11 Mar 2000 11:05:43 -0600, "Jackie, Meg and the kids" – Hide quoted text — Show quoted text -<hallerfa…@muscanet.com> wrote: >Joanne, > Is it possible to get a "digest" version of this. My inbox is kind of >overflowing from the rest of the stuff I get now. > Thanks, Jackie >"Joanne" <joa…@frsw.freeserve.co.uk> wrote in message >news:38c55708.9006365@news.freeserve.net… >> Hi >> This is just to let people know about our lupus email group. We have >> over 70 members from all over the world, all who have lupus, or are >> families of lupus patients. >> People can get support, advice, make new friends, through the group. >> It does generate a lot of emails every day, so be warned >> You can join the group by sending an email to >> uklupus-subscr…@listbot.com >> or you can join through my website at www.uklupus.co.uk >> We also have a lupus chat email group that is just for sharing poems, >> jokes, stories, general chit-chat etc. >> To join send email to lupuschat-subscr…@listbot.com >> or through the site as before. >> Joanne >> www.uklupus.co.uk
Response:
I am 43,female was dx with sle in9/98 and am now dealing with cerebritis. Have had 1 chemo tx with cytoxan and he next one is 3/20, no changes in my labs, but are waiting for more this week and have more to draw on friday. The docs have tried every drug combo they know, my rheumatologist called me a "rare bird" as far as getting any rise in my C3-53 and my wbc-500, neutrophils-.77. this computer was a gift from my husband because we live in very rural area in Illinois, and I have no one to talk with. I am an RN of 20+ years and never thought I would have to deal with this sle—my specialty was ob/gyn,but have not worked since Feb. 99 due to work and the drugs just battled me down to nothing–something had to go and it wasn’t the sle. Am desperate to establish with a link of others who are dealing with sle in any phase. Because I "fog" so much I am going to give you my e-mail cause sometimes I can’t remember where the chat room is. I’m at kim…@comwares.net and you can e-mail anytime. Thankyou for reading this and I hope I can return your support with my own. kim * Sent from AltaVista http://www.altavista.com Where you can also find related Web Pages, Images, Audios, Videos, News, and Shopping. Smart is Beautiful
Response:
Hi This is just to let people know about our lupus email group. We have over 70 members from all over the world, all who have lupus, or are families of lupus patients. People can get support, advice, make new friends, through the group. It does generate a lot of emails every day, so be warned You can join the group by sending an email to uklupus-subscr…@listbot.com or you can join through my website at www.uklupus.co.uk We also have a lupus chat email group that is just for sharing poems, jokes, stories, general chit-chat etc. To join send email to lupuschat-subscr…@listbot.com or through the site as before. Joanne www.uklupus.co.uk
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