Platelet Disorder Support Association

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!!! DISCUSSION GROUP RULES !!!

1. You must be a registered website user in order to post and comment. Guests may read only.
2. Be kind and helpful, not rude and cynical.
3. Don't advertise or promote anything. You will be banned from the group.
4. Report problems to the moderators. THANK YOU!

Hi

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14 years 10 months ago #14 by DebbieC
Hi was created by DebbieC
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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  • 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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14 years 10 months ago #26 by youngjoan
Replied by youngjoan on topic Re: Hi
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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14 years 10 months ago #27 by julia
Replied by julia on topic Re:Hi
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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14 years 10 months ago #45 by tofer
Replied by tofer on topic Re:Hi
ohhhhh it's spooky over here.... :evil:

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14 years 10 months ago #46 by DebbieC
Replied by DebbieC on topic Re:Hi
Hopefully it will feel like home someday. I hope that more people come here. Have a good Friday, Debbie

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14 years 10 months ago #51 by CindyL
Replied by CindyL on topic Re:Hi
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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14 years 10 months ago #52 by CindyL
Replied by CindyL on topic Re:Hi
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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14 years 10 months ago #60 by Jenuk
Replied by Jenuk on topic Re:Hi
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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  • 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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14 years 10 months ago #81 by Sandi
Replied by Sandi on topic Re:Hi
Spooky? Do you not get out much? :woohoo:

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  • 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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14 years 10 months ago #82 by Kim
Replied by Kim on topic Re:Hi
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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14 years 10 months ago #87 by DebbieC
Replied by DebbieC on topic Re:Hi
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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  • 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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14 years 10 months ago #94 by Sandi
Replied by Sandi on topic Re:Hi
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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  • 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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14 years 10 months ago #111 by Angel85
Replied by Angel85 on topic Re:Hi
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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  • 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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14 years 10 months ago #115 by Sandi
Replied by Sandi on topic Re:Hi
Hi Jen! I'm glad you kept your same name!

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14 years 10 months ago #124 by Jenuk
Replied by Jenuk on topic Re:Hi
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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14 years 10 months ago #125 by Jenuk
Replied by Jenuk on topic Re:Hi
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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14 years 10 months ago #144 by CindyL
Replied by CindyL on topic Re:Hi
How did I manage to get 2 posts of my replies? :huh:

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