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Thread: A little news about Sally (Salpalsally)

  1. #1
    Distinguished Community Member agate's Avatar
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    Default A little news about Sally (Salpalsally)

    Many have been asking about Sally for quite a while. There didn't seem to be any way to find out anything but I occasionally look at her daughter's Facebook page. A few days ago someone asked how her mother was doing, and I chimed in and asked as well.

    Today there was a reply. Sally has "gone to technology free as she says it's not fun any more." The daughter will let her know everyone says hello.
    MS diagnosed 1980. Avonex 2002-2005. Copaxone 6/07 - 5/10.
    Member of this MS board since 2001.

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  3. #2
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    Thank you, Agate! I was just thinging about her yesterday. I hope she gets less depressed and joins in again. She can travel the world on her screen.

    ANN
    There comes a time when silence is betrayal.- MLK

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  5. #3
    Distinguished Community Member Howie's Avatar
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    Cool

    I hope she will join us again. We have missed you Sally!
    Roswell was a gift.

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  7. #4
    Distinguished Community Member BBS1951's Avatar
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    Me too, I miss Sally here. I am hoping her leaving tech world is a good choice for her though.

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    Distinguished Community Member Jeanie Z's Avatar
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    Smile

    :) I send her a card every couple of months. I have her address if you need it PM me. Jeanie :)

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  11. #6
    Distinguished Community Member Earth Mother 2 Angels's Avatar
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    ((((((Sally)))))) ~

    You are truly missed here. But I certainly understand needing a break from technology.

    I'm just grateful to know that you're okay. I hope you feel all of the love from your friends here surrounding you and know that you are in our hearts forever.

    Love & Light,



    Rose

    (PS ~ agate, if you could perhaps convey our thoughts here to Sally's daughter, maybe she could share them with Sally to cheer her ~ thank you for sharing this with us ~)
    Mom to Jon, 48, (seizure disorder; Gtube; trache; colostomy; osteoporosis; hypothyroid; enlarged prostate; lymphedema, assorted mysteries) and Michael, 32, (intractable seizures; Gtube), who were born with an undiagnosed progressive neuromuscular disease and courageous spirits. Our Angel Michael received his wings in 2003 and now resides in Heaven. Our Angel Jon lives at home with me and Jim, the world's most wonderful dad.

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  13. #7
    Distinguished Community Member agate's Avatar
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    Rose, I have Sally's address and will definitely send the comments to her directly.

    As I understood it a while back, at the facility Sally is in, she has only her iPad for Internet access, and she was finding it hard to deal with. It's not ideal if you want to post on message boards, IMO. I keep hoping there will be a real computer in her life somehow.

    In the building I live in, called a retirement community, there are 3 computers with wi-fi access that are available to any resident who wants to use them. Many (like me) have their own computers but those who don't use those "public" ones. I have an impression that the place where Sally is doesn't offer this kind of thing, or she's confined to bed to the point where it's not possible for her to get to it.
    MS diagnosed 1980. Avonex 2002-2005. Copaxone 6/07 - 5/10.
    Member of this MS board since 2001.

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  15. #8
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    Sally has a Macbook Air. Or what ever the "Air" Apple computer is called. I never understood why it wasn't w her at this nursing home. I don't know if it was too physically challenging or too emotional.

    I miss her.

    ANN
    There comes a time when silence is betrayal.- MLK

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  17. #9

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    She was "technically challenged" when living in her own home. I appreciate how challenging it is to try to log in here from a different source of different computer. She is missed , though..

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  19. #10
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    I always thought as the years went on that Sal became a real wiz on the computer. She gave advice and helped others.

    The switch to a Mac after many years w a pc was hard at first, tho.

    ANN
    There comes a time when silence is betrayal.- MLK

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