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Hi 13 years 4 months ago #14

  • DebbieC
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It looks like I might be the first to post here. It took me a few minutes to figure out how to get in here. I had to go to the old discussion board. Hopefully everyone will find their way in here. Debbie

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Re: Hi 13 years 4 months ago #26

  • youngjoan
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  • I founded PDSA after recovering from ITP (7 failed treatments,zero count.) Read my story on the web site (search on 'success story.)Read more about me and my book, Wish by Spirit, at www.joanyoungwrites.com
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Debbie,

Welcome to the new group. It does take a little getting used to, but pretty easy once you figure it out....Any help you can provide to others is welcome....Joan

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Re:Hi 13 years 4 months ago #27

  • julia
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Hi Debbie & Joan, thought i better try it out before the other closes down! I feel very Autistic for the change at the moment. :ohmy:
Julia

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Re:Hi 13 years 4 months ago #45

  • tofer
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ohhhhh it's spooky over here.... :evil:

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Re:Hi 13 years 4 months ago #46

  • DebbieC
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Hopefully it will feel like home someday. I hope that more people come here. Have a good Friday, Debbie

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Re:Hi 13 years 4 months ago #51

  • CindyL
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I kinda like this new site. It's a lot more colorful! I think we'll get used to it in time.



Have a great day.

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Re:Hi 13 years 4 months ago #52

  • CindyL
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I kinda like this new site. It's a lot more colorful! I think we'll get used to it in time.



Have a great day.

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Re:Hi 13 years 4 months ago #60

  • Jenuk
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Well Debbie, you beat me to it being first to post here. Someone may remember I was the first person to sign up on the other forum when it changed over from the very old style forum. It was hard to change over, but in the end it worked so much better. Just did not get here quick enough this time ay!

Has this been planned for a while? Must look in more often!

Anyway, good luck with it Joan and Sandi. :side:

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Re:Hi 13 years 4 months ago #81

  • Sandi
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  • Sandi Forum Moderator Diagnosed in 1998, currently in remission. Diagnosed with Lupus in 2006. Last Count - 344k - 6-9-18
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Spooky? Do you not get out much? :woohoo:

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Re:Hi 13 years 4 months ago #82

  • Kim
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  • Diagnosed with ITP in 1983, lupus in 1990, APS in 2001, vasculitis in 2006. Current platelet count 148. In 2007 I had a stem cell transplant for autoimmune disease and currently ITP and APS remission, with a reduction in lupus activity.
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Hi there, although I'm Kim here, no longer Kimil, figured I have not lived in IL for so long, I should drop the il, but it's me, now just Kim and I'm from Wisconsin, been here 5 years, so now is a good time to change and since I was one of the first to register, I get to be Kim. I had to be Kimil on the other forums, because there was another Kim.

I like the new forum boards, seems easy to me, except for a few little things I'll have to get used to. I don't like having to log on each time and I wish when I clicked the link in the email notice it would just take me there, without having to log on. I find it easier to read through the posts and I love the option for email notice when someone posts to a discussion I'm following.

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Re:Hi 13 years 4 months ago #87

  • DebbieC
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Hi Jenuk, This has been planned for a while but it happened all of a sudden. I was surprised. I was only the first person to post on the Social Chat site here. I hope people will like this format and find it easy to use. I am getting used to it. Have a good week-end, Debbie

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Re:Hi 13 years 4 months ago #94

  • Sandi
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  • Sandi Forum Moderator Diagnosed in 1998, currently in remission. Diagnosed with Lupus in 2006. Last Count - 344k - 6-9-18
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Kim:

They are working on allowing Log-ins to last longer. Quite a few kinks to work out, but getting there.

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Re:Hi 13 years 4 months ago #111

  • Angel85
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  • I am 27 years old from Australia and I have T.A.R Syndrome. My email address is not showing on my profile for some reason so it is blossom_242@hotmail.com for anyone who wants to send me an email.
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Hi

I don't mind the new forum too much, just wish they could transfer all the old threads over so that we don't lose all that information that is already there.

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Re:Hi 13 years 4 months ago #115

  • Sandi
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  • Sandi Forum Moderator Diagnosed in 1998, currently in remission. Diagnosed with Lupus in 2006. Last Count - 344k - 6-9-18
  • Posts: 12436
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Hi Jen! I'm glad you kept your same name!

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Re:Hi 13 years 4 months ago #124

  • Jenuk
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Sandi wrote:

Spooky? Do you not get out much? :woohoo:


To be honest No, I don't...just not well enough these days.


Is the old site staying up?

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Re:Hi 13 years 4 months ago #125

  • Jenuk
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Post 2:

It looks quite good here, more cheery and lots of play things LOL.

Hope it does as well as before..I often use the treatment pages etc, so hoping I'll learn to navigate :side:

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Re:Hi 13 years 4 months ago #144

  • CindyL
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How did I manage to get 2 posts of my replies? :huh:

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