MarionSorell

  • peggy replied to the topic Useless legs in the forum Newcomers 9 years, 5 months ago

    Hi Calray,

    I too had problems with ‘useless’legs but I’d like to give a bit of history first.

    My diagnosis of myeloma occurred in a very roundabout way. I’d suffered increasingly severe migraines and noticed that I had difficulty raising my right leg so that I’d have to pull it up with my arms in order to cross a stile. It was discovered that my…[Read more]

  • peggy replied to the topic I need encouragment in the forum Treatment 9 years, 6 months ago

    Hi Susie,

    I too suffered from cramps. I mentioned it to my consultant who prescribed quinine tablets. Alternatively, it was suggested that if I didn’t want to take another medication I could drink a lot of tonic water as it too contains quinine – but she couln’t quantify what a lot was ….just to drink like a fish. I took the tablets and didn’t…[Read more]

  • peggy replied to the topic Low platelets in the forum Side-effects 10 years, 3 months ago

    Hello Eve,
    Sorry to hear about Slim’s predicament.
    I’ve been trying to recollect my treatment, it was some time ago now. I believe I was diagnosed approx June 2011 and went straight to RCD on the myeloma X1 trial. After quite a few major hiccups,and receiving six doses of Velcade to get my light chain readings down, I proceeded to my SCT. I don’t…[Read more]

  • peggy replied to the topic Loss of appetite in the forum Side-effects 11 years, 1 month ago

    No suggestions concerning the appetite..mine came back fairly quickly and I've regained nearly all the weight that I lost. However, regarding the lack of saliva when I was in hospital I was given a spray to replace the missing saliva. I only needed it temporarily but maybe you could get a prescription for something similar from your doctor. I most…[Read more]

  • My platelets went down to 2……….. but I,ve just read that I,,ve been, beaten, by Sue whose levels fell to just 1!
    All the best
    Peggy

  • peggy replied to the topic light chain myeloma in the forum Newcomers 11 years, 3 months ago

    I too have light chaiins…….in fact aI thhink that there are a fair number of us on this forum. I TOO had RCD but am onnly just recovering from my SCT which I had over Xmas ….truth be told I,m still feeling pretty rough. So neither have i reached the point of randomizattion either.

    All the best meanwhile,…[Read more]

  • peggy replied to the topic Charity night result. in the forum General 11 years, 4 months ago

    brilliant
    result
    …well doone
    peggy

  • I'm in now and have been for the past five days but have had trouble connecting up on the internet. I'm not being allowed home after the chemo as my kidney's state is such that I require careful monitoring.. A good thing too as I have constantly felt nauseaus from day 1 and have been on almost constant drips of anti emetic drugs and…[Read more]

  • Well, I thought that I'd be way behind some people here in having my SCT but it seems that I've jumped the queue. I was phoned up and asked if I'd like to accept a cancellation and I agreed.

    Initially I was to have my chemo on the 6th December, be sent home, to return on the 11th for isolation. but then I received another phone call saying…[Read more]

  • That believe it or not is what I,m currently hoping for. I,ve had enough of tests and procrastination….
    Diagnosed in April/May 2011 I am still awaiting my SCT. There have been good resons for the delay but enough is enough. I,ve had my cells harvested last week (3 days on the apheresis machine, following oone night on a trolley in A…[Read more]

  • (Hi Lizzy,

    I too was one of those unfortunate ones to have an allergic reaction to Allopurinol. The hospital wasn,t at first sure whether it was the Allopurinol or the Revlimid but I too took the risk of taking Revlimid again and luckily i had no further reactions. But I was hospitalised for over three weeks, had severe swelling of face body…[Read more]

  • peggy replied to the topic Confused in the forum Treatment 11 years, 6 months ago

    Hi all,

    Yes, I,ve got the answer. Dai, ther,s to be no chemo-priming. But I have got the GCsF injections. I had thought that I would have more hospital appointments and more tests but I was simply handed eight syringes to inject myself with starting on the day four days before the stem cell collection. That,s no problem but is that…[Read more]

  • peggy replied to the topic Confused in the forum Treatment 11 years, 6 months ago

    Thanks Eve And Helen for your responses…

    Roll on tomorrow when I will find out what,s happening. It,s school holidays this week so we,re going away for a few days and the following week I have a few non-alterable (non-medical ) appointments so no time to fit in any further medical tests… Tomorrow will reveal all.

    Peggy

  • peggy started the topic Confused. in the forum Treatment 11 years, 6 months ago

    I have an appointment tomorrow with my cosultant to sign consent forms for my sct etc. so I will ask him but meanwhile I am very confused..

    I am on the myeloma xi trial, was randomised to get velcade, and have just completed 5 cycles of this.
    On Friday I was told that i was ready for progression t SCT. Two days have been set…[Read more]

  • peggy replied to the topic Hair in the forum General 11 years, 7 months ago

    I'm just started cycle 5 of VCD. I noticed my hair start thinning on cycle 2. By cycle 3 it was coming out in handfuls, usually a day or two after taking the cyclophosphamide component of the VCD. On Tuesday I took my last cyclophos and guess what is happening this morning?

    I used to have longish hair but now it's dead short especially at the…[Read more]

  • peggy replied to the topic Colin the sequel SCT in the forum Treatment 11 years, 9 months ago

    Hi Vicki, I hope all goes well for Colin over the next few weeks. I'm still keeping my fingers crossed that I'll be
    following the same path in a few weeks time….. (last time I saw my consultant a few weeks ago I was prepared to be told that I could go in for the sct and then being on the Myeloma X1 trial I was 'randomised' to…[Read more]

  • Ah ,Kinder Scout Downfall. I have memories of climbing up the frozen waterfall at full moon with ice axe and crampons….my only true ice climb, Happy days,

    Peggy

  • Long before I mm diagnosis I started experiencing problems with leg movement. I used to enjoy going for rambles in the country but had difficulty getting over stiles.. It got to the stage that I had to physically lift my leg byputting my hands under/behind my knee and lift over.I was referred to a neurologist but he could find no explanation.…[Read more]

  • Hi all,

    I too had that dreaded allopurinol reaction………. started off with a rash and then my skin started peeling off all over. Unfortunately I was given an antibiotic which itseemsthat I was also allergic to and ended up in hospital for over three weeks. So no allopurinol, no meropenem, no erythromycin, no trimethoprim and no…[Read more]

  • Just back from a bone marrow biopsy: had sedation this time as on previous occasion it was extremely painful. I thought I was aware the whole time but doctor said that I was snoring : whatever, no probs this time.
    Now awaiting the results with trepidation…was told last consultation that mm had not responded well enough to chemo for immed sct…[Read more]

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