jennythomas

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Viewing 7 posts - 1 through 7 (of 7 total)
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  • #93798

    jennyanne
    Participant

    Dear Paul and Gayle. It was really nice talking to you at the Cardiff I.D.
    Hope to meet you again . If you drop me an email i can keep you in touch with whats going on at our Support Group.
    Best wishes.
    Jenny

    #93796

    jennyanne
    Participant

    Hello, It was lovely to meet you yesterday. We also enjoyed the day. M.U.K. do an excellent job. It is also great to have the chance to talk to other people in the same situation.
    Look forward to seeing you agaain sometime. Good luck with starting treatment.
    Jenny

    #93792

    jennyanne
    Participant

    Hello, There will be quite a few of us from the Support Group based in Cardiff attending the Info Day. My name is Jenny and I am SG leader for the group, my husband has had Myeloma for nearly 7 years. look forward to meeting you.
    Best wishes .Jenny

    #86585

    jennyanne
    Participant

    Dear Andrea, Our next meeting is on 13th Sept 7pm. If you would like to give me a ring i can give you more details. Also you can ask MUK if you can be added to our S.G mailing list then you will be kept in touch with what is going on. Look forward to meeting you.
    Jenny

    #86583

    jennyanne
    Participant

    Dear Andrea, Just thought i would let you know that we have a very active Myeloma Support Group in Cardiff. Quite a number of people who come to our group live in Newport and attend the Gwent.
    If you would like to phone/email or come to one of our meetings, you would be very welcome. Our details are on the website under Support Groups- Cardiff.
    Best wishes.
    Jenny

    #98650

    jennyanne
    Participant

    Dear Helen . Quite a few people in our group attend UHW and have had transplants there, including my husband in OCT 06.
    If you would like to contact me about the group, my details are on MUK site under Support Groups. You can also contact the Info Line as they have a Peer Network service and can put you in touch with someone who has been through it.

    #98648

    jennyanne
    Participant

    Hello Helen. I haven`t heard of any link between Prostate Cancer and Myeloma. We have a Myeloma Support Group based in Cardiff . Our next meeting is on Thursday 12 January. If you and your fiance would like to come along and meet other people in the same situation or talk to someone who has gone through S.C.T.we would be very pleased to see you.

Viewing 7 posts - 1 through 7 (of 7 total)