Family member of BCD patient

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  • #1556
    MiukieMiukie
    Participant

    Hi All!

    Thank you for inviting me to this community. I’m so grateful to be here.  I am here to understand and learn more about BCD so that I can help my loved to cope with his current situation.

    #1557
    MiraMira
    Participant

    Hi, welcome and thanks for joining.
    Please feel free to ask any questions – also those subjects not yet discussed.
    //Mira

    #1565
    MiukieMiukie
    Participant

    It’s not easy to cope with your loved one which have diagnosed with BCD and in denial mode.  I feel so helpless most of the time and unsure what can I do to make him feel better.  Sometimes I wish that the person that gotten such disease would me not him.

    #1600
    IC57IC57
    Participant

    Hi,

    Thanks for inviting me here and developing the great website to spread awareness.

    Since there is no cure yet, I feel engaging more in physical activities (running, yoga) and trying to stay mentally healthy are the two things helping my loved one to delay progressing the disease.

    I hope to learn more about other patient’s experiences and thing they are doing to cope up with BCD.

     

    #1602
    MiraMira
    Participant

    It is devastating to see your loved ones suffer, without being able to help them.

    When in denial, there is nothing you can do, the same goes for BCD. Unfortunately😔

    My best advice is for you to mentally prepare, to ‘catch’ him when he comes out of denial. To stay mentally and physically fit is essential! I also think encourage him to to sports and enjoy his most precious interests, will help him a lot. Maybe exploring new interests that does not require the perfect vision.

    Best wishes.
    //Mira

    #1685
    BonsmomBonsmom
    Participant

    Hi, I’m new one here. I’m Lily, a daughter of BCD patient.

    My English is not so good. So if I’ve said something improper, please let me know, thanks.

    I can’t agree with #Miukie any more. Your situation is as same as my mom, so I tried to be the mediator.

    Base on his psychology or the mood, it’s so hard for us to know whether he needs our help.

    I start to pay attention on which he is interested in and make more conversation with him to make him feel  not so lonely.

    Maybe this can give you a little help.

     

    This is such a long way for both patients and their family members.

    Fortunately, thanks to all who work so hard for BCD , we still have them and each other.

    Just keep working, and relax yourself as well.

     

    Lily

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