ElizabethLaw

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Viewing 15 posts - 136 through 150 (of 308 total)
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  • #92137

    Elizellen
    Participant

    Have a lovely time in Venice, Val!

    I went there a couple of times in the 60's and would love to revisit as there was so much to see in such a small area.

    Eliz
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    #98802

    Elizellen
    Participant

    Like everyone else I was so sorry to read of your latest news, Bridget. 🙁

    Sending you cyberhugs

    Eliz
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    #92172

    Elizellen
    Participant

    Hi Glenn!

    I was wondering how your kyphoplasty operation went and how you are feeling now.

    Eliz
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    #98892

    Elizellen
    Participant

    Fantastic News, Tom!! 😀

    Long may you stay treatment-free!!

    Eliz
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    #92228

    Elizellen
    Participant

    Great to be able to put a face to the name, Mavis!

    Eliz
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    #106953

    Elizellen
    Participant

    Hi Penny
    I am one of those lucky ones who had almost no problems during my SCT proceedure, so it is not inevitable for you to get sore throat, and diarrhoea, you might be like me and sail through with nothing much in the way of nasty side effects.

    During my stem cell return I was told to suck ice lollies which was supposed to minimise the mouth/throat etc problems, and the ward had a stash of ice pops and lollies which I duly worked my way through while watching my cells drip into me.

    AS to how you might feel about getting back to work post SCT, if I had not got disintegrated vertebra resulting in pain when standing and walking (which was the reason for seeing the doctor and getting diagnosed) I think I would have been fine to carry on working about a month after treatment once I got my energy back.

    I was a good bit older than you are (60) so I hope your yuunger body and fitness level helps buoy you up throughout your hospital stay.

    Wishing you an uneventful hospital experience when it happens

    Love from
    Elizabeth
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    #92142

    Elizellen
    Participant

    Hi Terry, I think my post was one of the missing ones, so here I am again.

    Apart from welcoming you to the club none of us asked to join, I think I suggested in that post that you should mention to your consultant and medical team the problems that you experienced the last time you were in hospital.

    If you tell them plainly how if felt to not be warned before someone touched you then hopefully they will make sure that all their staff are told not to surprise you by sticking anything in you without warning!!

    It would not take much effort for someone to stick a note on the door or beside your bed giving instructions on how to approach you, so temporary staff are made aware and can behave appropriately.

    Eliz
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    #110137

    Elizellen
    Participant

    Here in Bournemouth our snow was a bit of a "damp squib" as though it fell in the night (I noticed a covering on the cars outside when on one of my "loo trips") it had completly vanished this morning.

    #98365

    Elizellen
    Participant

    What great news!

    I hope it won't be long till everything is in place to allow you to have more control over your schedule!

    Eliz
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    #98729

    Elizellen
    Participant

    Wow, Henry did really well to get enough cells in one go!
    It took me three days and still I only just yielded enough for one procedure. 🙁

    Feel free to post a link for the fundraising your daughter is going to do and thank you to her for her support for myeloma uk.

    #92067

    Elizellen
    Participant

    In case you missed it, Lin, I just noticed some posts towards the end of this thread
    http://www.myeloma.org.uk/patient-services/discussion-board/general/catching-up/

    which mention various insurance companies and members' experiences with getting the right insurance

    #110088

    Elizellen
    Participant
    #85157

    Elizellen
    Participant

    Hi Christine!

    I was diagnosed at the beginning of 2010 because of intense back pain which had been caused by 3 vertabrae collapsing at once. Since then several more vertebrae have gradually deteriorated.

    They decided to do chemo then a stem cell transplant immediately to zap the MM so did not look into doing a balloon kyphoplasty initially and I am still awaiting the verdict as to whether they can do anything now I am in remission to alleviate my back pain by some kind of surgery.

    Apparently I have a few bone fragments floating near the spinal chord that they are worried about disturbing and shifting the wrong way, so it might not be a possibility.

    I have a nagging back pain most of the time but it only becomes unbearable if I stand, bend over a workbench or walk for 20 minutes or so. So I can do quickly finished stuff if I plan things and make sure I can sit down frequently which seems to lessen the pain.

    I haven't found a painkiller that really works so on the whole I manage without, as I would rather put up with a bearable pain than suffer the constipation etc which most painkillers gave me.

    I have a retail shop selling stained glass supplies and though I do not have regular opening times any more I still manage to open for an hour or so when people contact me to arrange it, so am still working some of the time and keeping the business ticking over. If I had a sitting down job I reckon I could manage to carry that out OK with little disruption.

    I manage to drive fair distances and walk around the supermarket to get my shopping (I always use a large supermarket trolly even if I am not buying much, as part walking frame/part trolley) so can get out and about to my old haunts, so do not feel too restricted in daily life.

    We bought a mobility scooter when I was first diagnosed which I do use to get to hospital appointments (Bournemouth Hospital corridors are very long!!) and for longer shopping excursions, so if that might be useful to help you get around do look into getting one. We bought ours on ebay for very little money, as well as a vehicle hoist so I can get it in and out of the car on my own.

    So for me it has not been the end of all my previous interests and occupation.

    Wishing you all the best on your myeloma journey!

    Elizabeth
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    #98570

    Elizellen
    Participant

    What terrific news, Tom!!

    #107347

    Elizellen
    Participant

    I am glad you seem to have got some benefit from the session and are planning towards the next one, Roz.
    Writing it all out is a way I often get to grip with things as it seems to help things fall into place.
    Sending you cyberhugs {{{{{Roz}}}}} and my love.

    Eliz
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Viewing 15 posts - 136 through 150 (of 308 total)