Parkinson’s Disease and how my thinking has changed when medication doesn’t control symptoms

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  • เผยแพร่เมื่อ 29 พ.ย. 2024

ความคิดเห็น • 31

  • @davinagauthier6396
    @davinagauthier6396 6 หลายเดือนก่อน +2

    You haven't lost your sense of humor..that's so encouraging...

  • @GaryPack-l4u
    @GaryPack-l4u 4 หลายเดือนก่อน +2

    Your sharing is really valuable. You are a voice for many.

  • @lisaa6099
    @lisaa6099 5 หลายเดือนก่อน +3

    Thanks. Bless , keep up the videos……. The fear of the future is what i have also so thanks for saying that

  • @JeremyMcdonald
    @JeremyMcdonald 10 หลายเดือนก่อน +3

    The worst choose your own adventure! Perfect!

  • @alecspeer
    @alecspeer 8 หลายเดือนก่อน +2

    I am diagnosed with Parkinson's Disease in 2019. I am 76. There is currently no cure for PD.
    I am a patient of a neurologist who is a specialist in movement disorders, and he diagnosed me as having PD.

  • @audiotech6513
    @audiotech6513 8 หลายเดือนก่อน +1

    Nice to see your video i am with you i hv been diagnosed since 4months now for hand tremor n feel the same i am guy 70 years but PD is different for different people i guess…. You are a long way for DBS so enjoy life in the meanwhile n keep up your videos

  • @LifewithParkinsons
    @LifewithParkinsons 9 หลายเดือนก่อน +1

    Hi Esther, I did not realize you had a TH-cam channel. Mostly watched you on Tik Tok. Just watching you and Jeremy chatting. Will share your channel.

    • @shakinginmyboots1
      @shakinginmyboots1  9 หลายเดือนก่อน +1

      Hi! I just started as an easy way to post my TikTok’s on Twitter (X) originally. But realized TikTok time limits kind of suck when I want to really talk about stuff in detail. So here I am on TH-cam. This makes sense though as I see there are a lot of Parkies on here. Love your stuff!

    • @LifewithParkinsons
      @LifewithParkinsons 9 หลายเดือนก่อน +1

      @@shakinginmyboots1 I agree, I find Tik Tok very restraining and difficult to gain a solid footing with content more than 1 minute long. TH-cam has a great community and I feel strongly that there are not enough quality channels to fit the demand, so I am glad you are here.

  • @paulsteffan2703
    @paulsteffan2703 5 หลายเดือนก่อน +1

    Biggest problem- dosing to level. I take sinemet 75 mg every 2 hrs. Spend half the day up and half the day down. I’m 60 and I’m busy . This dosing regiment sucks. Hoping for DBS

  • @craigkeller
    @craigkeller 5 หลายเดือนก่อน

    Brave and real.

  • @timball3026
    @timball3026 8 หลายเดือนก่อน

    Thank you for being real

  • @jonathanstapleman2112
    @jonathanstapleman2112 6 หลายเดือนก่อน

    I have a DBS and I'm so glad I did. My Leva Dopa dose is cut back 50%

  • @raymondviccaro7489
    @raymondviccaro7489 5 หลายเดือนก่อน

    Talk to your neurologist about focus ultrasound for your tremor.

  • @nedaward3032
    @nedaward3032 7 หลายเดือนก่อน

    Have you thought about mri based ultrasound to treat the tremor?

    • @nedaward3032
      @nedaward3032 7 หลายเดือนก่อน

      Just heard your next sentence! lol. I guess you did.

  • @roberttomasetti3654
    @roberttomasetti3654 9 หลายเดือนก่อน +2

    Hi Ester, same here first years after PD diagnosed. I discovered that you have to take each dose of the carvidopa-levidopa at exact intervals. Tremors are under control. Please don't overdose, it has some nasty side effects. I am a member of the Michael J. Fox Foundations Network of Care, it's free. Check it out. Good advice from members in treatment.

    • @tootalljones77
      @tootalljones77 6 หลายเดือนก่อน

      B.S. life isnt "exact" If I'm going into an important meeting or a social gathering, there's definitely a difference from being home alone, or at the gym. Everyone s different
      I take it according to my daily activities.

  • @puttentanesame6687
    @puttentanesame6687 8 หลายเดือนก่อน

    Acupressure massages.

  • @stevesilia9175
    @stevesilia9175 8 หลายเดือนก่อน

    You got dyskinesia after six months on the medication ?

    • @shakinginmyboots1
      @shakinginmyboots1  8 หลายเดือนก่อน

      Sooner actually, didn’t really know how it felt in the beginning. Thought it was something else, but yes I developed what’s know as “wearing off” dyskinesia almost immediately.

    • @stevesilia9175
      @stevesilia9175 8 หลายเดือนก่อน +1

      So I am a 53-year-old male was just told I have Parkinson’s i’ve got a slight tremor in my left hand they want to start me on the medication but I’m a bit hesitant

    • @shakinginmyboots1
      @shakinginmyboots1  8 หลายเดือนก่อน

      th-cam.com/video/v-LzJb3DcIg/w-d-xo.htmlsi=HCOMzKyQs-5HNS1A

    • @shakinginmyboots1
      @shakinginmyboots1  8 หลายเดือนก่อน

      @@stevesilia9175 it’s different for everyone. I found this video helpful. I started the medication to reduce my tremor for work. It really depends on so many things. There’s no right or wrong answer

    • @stevesilia9175
      @stevesilia9175 8 หลายเดือนก่อน

      @@shakinginmyboots1 Thank you so much ; I’ll let you know how it goes .

  • @judyhowell7075
    @judyhowell7075 4 หลายเดือนก่อน

    Foods!