Forum Replies Created

  • Angela

    Member
    October 25, 2022 at 10:57 am in reply to: Do you watch more TV than you used to watch?

    My husband used to watch TV as soon as he got home from work until bedtime and now it is on from 8am to 10 or 11 pm. He will take a break of an hour or so to do something. It is mind numbing and I wish the TV was off but I guess it gives him comfort.

  • Angela

    Member
    September 13, 2022 at 9:13 am in reply to: Body odor

    My husbands body odor has become more pungent. He showers but even the towels retain the odor. He as well has foul smelling flatus constantly which is overwhelming. I think it has something to do with constipation or something else.

  • Angela

    Member
    June 29, 2022 at 8:41 am in reply to: Best Mattress for PD?

    Hi,
    I’m not too sure of the brand names but my husband who has Parkinson’s got a really Firm mattress because he was unable to move out of position on a pillow top or mid firm . It hurts my back because it is so hard ( I may sleep in another bed) but he loves it and can get out of bed earlier. We just use a bottom sheet and a duvet over, He sleeps naked so there is no PJ’s to get caught in anything

  • Angela

    Member
    May 10, 2022 at 9:12 am in reply to: Care Partners/Givers Interested in Support Group

    Hi a once a month zoom meeting sounds reasonable . I am in the pacific zone ( Vancouver/ Seattle) and works days. What time were you thinking would work?

  • Angela

    Member
    March 24, 2022 at 9:17 am in reply to: Care Partners/Givers Interested in Support Group

    Hello,

    My husband was told that he had 5 years before he would lose all function. He is just 60. I am trying to find ways to support him. I am seeing a lot of his ADL’s slipping. I am worried about him driving and handling power tools. He is quite depressed and I find him sobbing quite a bit. I am 65, working at a emotionally stressful job with the homeless, have grandchildren and my own mental health problems. I find I am doing more and more of the household chores and it’s draining. When he doesn’t understand things on the computer or something he has read he panics and I have to drop everything to solve his problem.
    He refuses to use any mobility aids like a walker and I am afraid he will have a fall. He can’t handle anything that is not routine such as a birthday party or visiting his daughter who is in addiction. I think we could pool our resources via zoom. I am home by 630 pm usually BC time. Thanks

  • Angela

    Member
    March 16, 2022 at 9:21 am in reply to: overwhelming as a caregiver

    You must be so overwhelmed. I am a nurse who is watching my husband decline and have 8 grandchildren. My husband has the rapid form of Parkinson’s. I feel so overworked trying to take care of him, the house and all the grandchildren.
    I told him I feel like a single mom and he said well just pretend you are. I said this is a marriage. I don’t want to be the sole supporter of everyone.
    I keep going . That’s all I can do. I am 65 and feel like I will have to work for many more years to support my husband. I do get frustrated, cry and am depressed. I as well have my own health issues.
    I still try to carve out a little time for myself and just don’t come home right away after work.
    God is my help right now and I am praying he gives me the strength to carry on.
    Who knows maybe science will find a way to cure this terrible disease.

  • Angela

    Member
    May 15, 2022 at 3:06 pm in reply to: Care Partners/Givers Interested in Support Group

    Can you please send me the zoom link.