Any helpful tips on getting my legs to work again?

This topic contains 1 reply, has 2 voices, and was last updated by  katyg 1 year ago.

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  • #148368

    cwtx
    Participant

    I was diagnosed in June 23 and with a rapid decline, having to use a wheelchair. Since the the treatment started I then made a little progress and was able to walk short distances from room to room. But now in cycle 6 I am struggling with the fluid overload and feel like I have no leg muscles. Will I get some mobility back and if so how do I build up my muscles again. How have other people managed?

    #148464

    katyg
    Participant

    Hi CWTX, I’ve been thinking the same thing – my partner was also diagnosed in June, firstly with MM and then with Al Amy, which has affected his heart. After two cycles of Velcade, Cyclophosphamide and prednisolone, and four more to go, his mobility is very limited and he struggles to eat. The fluid on his lungs is now under control, and after the first cycle his light chains have reduced by over 70%. I think most people find the chemo gruelling!
    He wasn’t well enough to attend a physiotherapy appointment recently, but I imagine they’ll have some good muscle building exercises – we’ve started doing some at home anfter watching a couple of YouTube videos.
    A heart specialist suggested a pedal machine, the sort that fits under a desk, so that’s something Im going to buy as you can build up the resistance level gradually. He’s joined the Al Amyloidosis private Facebook group, and there are so many encouraging stories from people who’ve been in remission for years and are walking miles again, albeit slowly in some cases, and even running and returning to work. Sending you best wishes, Katy

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