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Re: Next chat

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That sounds fine to me. Just need a time. I guess 6pm PST would work

fine.

Also someone suggested a day time chat. I might be available for that

one too. I don't work, but seem to have a million appointments during

the day.

Wishing everyone wellness,

-Meghan

> would anyone like to chat on thurday the 18th night. let me know

and

> we can set a time.looking forward to it..............kyle

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i'd be up for a chat on thursday night ... between 8 and 10pm (EST -

with daylight savings!:)) is good for me ...

-michele

> would anyone like to chat on thurday the 18th night. let me know

and

> we can set a time.looking forward to it..............kyle

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I would be interested in joining. I am in Northern Ontario, Canada

so if it would be set at 9h00 pm, I'd be able to join in. Looking

forward to it.

Memine

> would anyone like to chat on thurday the 18th night. let me know

and

> we can set a time.looking forward to it..............kyle

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Ack!!! Did we have the chat on the 18th?!

I had it written on my calendar and everything and still forgot!

Ack!

If you had it, how did it go? How many people showed up?

said there's another one this coming Monday at 2pm EST, is that

right?

>

> > would anyone like to chat on thurday the 18th night. let me know

> and

> > we can set a time.looking forward to it..............kyle

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Hi. We did have a chat on April 18th,2002 and it was quite

interesting. We were 4 people from different places (Alaska,

Canada, USA. Another chat has been set for Monday at 2h00pm and

again at 9h00 pm. Hope to see you there. Memine

[

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  • 6 years later...
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Thursday Great for me Kathy Sweet I will be there

>

> Let have our next chat this thursday at 7pm est 4pm pst is everyone

ok

> with this time or give me suggestions? Majority rule any suggestions

> on timing and date? mike group owner

>

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What kind of Instant Messenger? There are so many.

In a message dated 7/27/2008 2:01:48 A.M. Eastern Daylight Time,

teenysjms@... writes:

Give Mike your email address, he will add it Instant messenger. When you

sign onto IM it will ask us if we want to add you to our list we answer yes or

no. When we log on to chat those that are logged on can talk by typing what

they want to say . what they type will show up on the screen by our name.

That simple.

a

From: _UCJAM1977@..._ (mailto:UCJAM1977@...) <_UCJAM1977@..._

(mailto:UCJAM1977@...) >

Subject: Re: next chat

_Stimulator@groStimula_ (mailto:Stimulator )

Date: Saturday, July 26, 2008, 10:31 AM

I don't understand how the chat works. Could you give me more information?

I would really like to participate.

In a message dated 7/26/2008 9:26:58 A.M. Eastern Daylight Time,

mike2boysmsn (DOT) com writes:

Ok next chat will be this sunday at 9pm est 6pm pst. I want to see a

huge turnout. mike owner

************ **Get fantasy football with free live scoring. Sign up for

FanHouse Fantasy Football today.

(_http://www.fanhouse_ (http://www.fanhouse/) .com/fantasyaffa

ir?ncid=aolspr00 050000000020)

[Non-text portions of this message have been removed]

[Non-text portions of this message have been removed]

**************Get fantasy football with free live scoring. Sign up for

FanHouse Fantasy Football today.

(http://www.fanhouse.com/fantasyaffair?ncid=aolspr00050000000020)

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Hi Mike,

My name is Sue Corn. I have RSD since l999. I'd like to introdroduce myself to

you and the rest of the group. I've been receiving your e-mails for quite a

while and decided to write in. I belong to a live support group and know how

very important a strong and loving support system is.

After my injury in 1999, I had 2 shoulder surgeries, which only made the

shoulder go from bad to worse. Like so many of you, I went from Dr. to Dr. to

Dr. to try to find out what was wrong with me. I got all the answers the rest of

you got, except the right one. It took almost 4 years to finally diagnois me

with RSD. By that time, I didn't have much mobility of my right arm and hand,

and as time was passing I was having a harder time walking. Because I hadn't

been diagnoised sooner, the RSD spread throughout my body.

I now have both a cervical and lumbal SCS and a Pain Pump. The only meds I

currently take are Topamax and Cymbalta. Trust me when I say, the journey has

been to hell and back. Before I started treating with the Dr.I now use I had

been on every med. out there. There was a time that I was so doped up that I

didn't realize how doped up I was until I got off the meds. I still have pain,

but the pain is more manageable. When the pain gets intolerable, I work through

it. I've accepted that I'll never be the way I was, but with the SCS and the

Pump it's so much better than I was before. I now have mobility of my arm, and

the SCS kept me out of a wheelchair. More of my story will unfold as time goes

on.

I would like to join the group. I hope to be able to join the chat tonight.

My e-mail address is: sueandtedc@...

NEVER GIVE UP HOPE

SUE

next chat

Ok next chat will be this sunday at 9pm est 6pm pst. I want to see a

huge turnout. mike owner

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Hi Sue,

Welcome you will love it here on the site we are all friendly and open.

Look forward to chatting and talking with you more.

Keep On Smiling

Kathy Sweet

next chat

Ok next chat will be this sunday at 9pm est 6pm pst. I want to see a

huge turnout. mike owner

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