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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

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Re/Dew58

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Old 01-23-2010, 04:26 PM #1
Breezy55 Breezy55 is offline
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Has anyone heard from Dew? I have sent her a few pm. However I have not heard back from her? Breezy55
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Old 01-23-2010, 05:12 PM #2
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Hi Breezy55,

I was thinking of the of the same the other day and check her page. She hasn't logged on since Nov. 1, 2009. I remember back then she said she wasn't doing well, that was why she wasn't posting. I hope someone can get hold of her and let us know.

Sandy

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Has anyone heard from Dew? I have sent her a few pm. However I have not heard back from her? Breezy55
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Old 01-24-2010, 02:40 AM #3
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Has anyone heard from Dew? I have sent her a few pm. However I have not heard back from her? Breezy55
I've also been concerned about Dew-I PM'd her a few times, I know it's been difficult to be dealing with WC. I think about her sister too-hoping she is still in remission with her cancer. She is so sweet-I'll write her again and hope to get in touch with her.

Breezy, I'll PM you too. I just contacted attorney yesterday regarding SSDI. So much going on right now. I've got some of the information ready to send you,like i Promised. Take care-loretta with soft hugs
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Old 01-25-2010, 08:31 AM #4
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I have Linda on my friend list on Facebook and she is always pretty active on it. She spends many hours a day playing on the games there etc. She hasn't posted much about her RSD but I know she recently went on a trip to see some relatives which she said took it out of her.

I'll tell her that you have all been asking about her and ask her to post when she feels up to it.
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Old 01-25-2010, 08:35 AM #5
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ali

are we allowed to post our full name so others here can friend us on facebook.? I need to get you and dew on my list


hugs
Mary

ps. The pump is wonderful. When I had the scs implanted, you may remember it was weeks before I wanted to get out of bed due to pain. With this. my family is threating to tie me to the bed. I want to get out and move... yea
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Old 01-25-2010, 08:47 AM #6
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ali

are we allowed to post our full name so others here can friend us on facebook.? I need to get you and dew on my list


hugs
Mary

ps. The pump is wonderful. When I had the scs implanted, you may remember it was weeks before I wanted to get out of bed due to pain. With this. my family is threating to tie me to the bed. I want to get out and move... yea
Just a reminder--- It is best for you and your privacy to use the PM function to send sensitive information to others here.
personal email addy
real name
addresses for card exchanges etc.
Birthdates etc.

If you put them up on the board itself a trolling bot from a search engine will pick it up QUICKLY and even if you remove it tomorrow, it might be too late and cached on Google forever!
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Old 01-25-2010, 09:25 AM #7
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Would you believe me if I said " I knew that" lol. Still recooping from getting the pain pump, and even tho my mind is starting to clear up from getting off my oral meds, I still don't think things thru like I used to. I'm hoping it gets better for me.

Hugs
Mary
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Old 01-25-2010, 10:04 AM #8
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Would you believe me if I said " I knew that" lol. Still recooping from getting the pain pump, and even tho my mind is starting to clear up from getting off my oral meds, I still don't think things thru like I used to. I'm hoping it gets better for me.

Hugs
Mary
Yes, I suspected you knew that. I have done unwise things at times myself, over the last 10 yrs! We can get so complacent here, at NeuroTalk, because we all know each other, that our guard might get rusty!

I remind people just so they stay safe! (and happy).
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