ElizabethLaw

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Viewing 15 posts - 106 through 120 (of 308 total)
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  • #85149

    Elizellen
    Participant

    Good to get an update of how Etta is doing, Craig! 😀

    I hope her date for an SCT comes soon so she can be over it and well enough to make the trip down under!

    Best Wishes

    Eliz
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    #86003

    Elizellen
    Participant

    Hello Jerry, I am sorry to hear of your father's ill health.

    There is lots of information on this website with leaflets you can download to read through that might help clarify what is possible.

    Click on this link and browse the various headings.
    http://www.myeloma.org.uk/patient-services/myeloma-uk-publications/

    Your English is excellent, by the way!

    Wishing your father and whole family all the best as you start this journey.

    Elizabeth
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    #92606

    Elizellen
    Participant

    Hello Ann!

    I noticed this is your first post here, so welcome to the club none of us ever imagined we would be eligible to join.

    I have not yet had Velcade (had CDT then a SCT in the summer of 2010) but think I recall other members here posting about having similar problems. I am sure some of them will soon post with their own stories of how this treatment affected them.

    My regards to your hubby too. Will he be coming here to read posts or are you the "computer geek" in your marriage? My husband can just about manage to play solitaire on a computer and do "brain training" on his Nintendo DS, so it is always my "job" to look stuff up for him if he wants to find info about his interests. 😉

    Eliz
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    #92419

    Elizellen
    Participant

    Great to hear your news, Wendy!!

    Long may it continue! 🙂

    Eliz
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    #107586

    Elizellen
    Participant

    Oh Eve, I am so sorry to hear the sad news of your family's loss.

    My thoughts and prayers are with you all at this difficult time.

    Eliz
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    #92593

    Elizellen
    Participant

    Is it only happening with newly uploaded profile pics, Sruart?

    Eliz
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    #92564

    Elizellen
    Participant

    I now live in Bournemouth and haven't visited The Wells since my Mum moved out of the old house in the St John's area in the summer of 2008.

    Have they improved the Kent & Sussex hospital since then?

    Eliz
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    #92562

    Elizellen
    Participant

    What a small world, Mari, as I lived in Tun Wells from the age of 5 (58 years ago) and we moved my Mum away from there only about 4 years ago.

    Eliz
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    #85843

    Elizellen
    Participant

    Welcome to the club which none of us asked to join, CharlieLouise, your nan is lucky to have such a caring grandaughter!

    I just had a thought about where you could ask those questions if it is not possible at the consultant appointment – I was allocated a specialist nurse when I was diagnosed and was able to contact her at any time with any questions/problems.

    If your nan is also given a SN then perhaps you can contact her when your nan (and the children) are not around so you can clarify things and ask any awkward/embarrassing questions.

    Also there might be a support group locally where you could attend meetings either alone or with Nan and meet others in the same boat to make friends. The SN should be able to tell you about any meetings.

    Hoping the MM journey that you are accompanying your nan along progresses well and uneventfully.

    Love
    Eliz
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    #92559

    Elizellen
    Participant

    Hi Carol!
    I am also on facebook now and again, use it mainly for posting family photos and keeping up wiht what they are doing rather than posting what we are up to. 😉

    Look for me as Elizabeth Law – at the moment I think I have the same profile picture as I have here.

    #92535

    Elizellen
    Participant

    Good to see faces instead of black aquares, Scott and Teresa!

    It helps to make the forum feel more friendly 🙂

    Eliz
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    P.S. Good clear instructions, Dai! Thanks for posting them.

    #99151

    Elizellen
    Participant

    Good spot, Jorge!

    It certainly looks like an error to me.

    Eliz
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    #85766

    Elizellen
    Participant

    Hello Neelie!

    It looks as if I was one of the lucky ones as my GP remembered about MM from his college days (one of his lecturers apparantly had done research on MM and must have been enthusiastic about it I suppose) and was quick to send me for tests as soon as I went to see him about my excruciating back pain, that would not respond to a week of painkillers prescribed by the locum I saw initially.

    Once all the tests had been completed things went quickly for me and within a few months I had a successful SCT. Now I am still in complete remission over 2 years after diagnosis and only need to see my consultant every three months!

    As well what Nicola suggested about writing down the questions I think of before an appointment one thing I do is take my mini voice recorder to all of mine so I can load the recording onto my computer and listen again when at home.

    So often on listening again I discover some info I had not picked up on during my appointment, or am reminded of something I had forgotten amidst all the whirl of info, dates and treatments being discussed.

    I posted in the General forum about a special offer for the one I have which is finished now 🙁 but the product is well worth even the full price I think.

    I wish your Dad and your family the very best at this strange unexpected turn of events in your lives.

    Eliz
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    #92435

    Elizellen
    Participant

    Eve asked[quote]I would like to know how you do the picture bit on here [/quote]It is quite simple once you have the url of the picture.

    First click on the url and copy it (press the Ctrl key and the letter C at the same time) then look above the text box that appears when you click "Reply" or "create new discussion".

    Just beneath the word "Message" are several buttons, the first 3 are for adding formatting like bold, italic or underline to letters in your post, the 4th is for adding a link, the 5th is for adding a picture, the 6th for making anything you type appear as a quote and the last is to add simple smileys.

    Click on the picture icon (looks like a tiny photo of a mountain with the sun shining) and a box will appear into which you can paste the link to your chosen picture by using the Ctrl+V keys.

    Simples!

    [img]http://1.bp.blogspot.com/-SrHVfDAYHg8/TjPAFT3S8GI/AAAAAAAABjQ/HrBbWZ7cCMg/s1600/simples.jpg[/img]

    Eliz
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    #99073

    Elizellen
    Participant

    Andy wrote[quote]Live life to the max![/quote]Great positive attitude, Andy!!

    Eliz
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Viewing 15 posts - 106 through 120 (of 308 total)