#109

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  • Опубліковано 8 лис 2024

КОМЕНТАРІ • 14

  • @Lenteja77
    @Lenteja77 4 місяці тому +4

    The patient is the best person to say when it’s needed to take the meds.

  • @joselugo1619
    @joselugo1619 4 місяці тому +1

    Interesting and great information on this

  • @nancilee53
    @nancilee53 4 місяці тому

    Great information. Thanks

  • @DannyCockrell-g5d
    @DannyCockrell-g5d 4 місяці тому +2

    Good information thanks!

  • @Lenteja77
    @Lenteja77 3 місяці тому

    Hello Jessica and Brian, my name is Silvina and I live in Austria. I am 60 years and I was diagnosed 12 years ago. I love your podcast, and I would like to suggest if you can do a research about the Parkinson’s gloves
    About two years ago it was on the news the presentation of the Parkinson’s glove discovered in the university of Stanford, CA. Very promising non-invasive treatment. I will send you the link in case you haven’t heard. They say that it will be on the market this year.
    The other topic that I would like to hear is about the addiction that many people develop with Parkinson’s, like gambling, shopping or even sex addiction. A Tabu topic that is real and no One Talk About it.
    Best regards and congratulations for your program

    • @thesecretlifeofparkinsons
      @thesecretlifeofparkinsons  3 місяці тому

      Hi Silvina! Yes, I remember the study with the gloves. While I was also excited, I then quickly learned the study was only done with like 4 people and they are in the very early stages of development. For whatever the reason, the news picked it up, which is frustrating because they are no where near ready for the market. Anyway, I'll keep an eye on it to see if anything new pops up.
      as for the addiction part, I only experienced it when I was on Ropinirole (dopamine agonist). We did talk about it in a previous episode but I'll have to get back to you on which episode that was. Yeah, the addiction is real, and it was awful.

  • @joselugo1619
    @joselugo1619 4 місяці тому +1

    I was diagnosed on May 8th and just started my medication this morning. Carbidopa/Levidopa 25/100 mg 3 times a day, starting off with half a tablet for the first 3 days. I was pretty nervous taking it today just because I didn’t know what to expect

  • @nancilee53
    @nancilee53 4 місяці тому +1

    Great

  • @wadehuffaker9327
    @wadehuffaker9327 3 місяці тому

    I don't use the Parkinson's drugs. I've had Parkinson's for 14 years. I got to stage 3 and reversed back to almost no symptoms at all.

    • @milaloeb977
      @milaloeb977 3 місяці тому

      Doing what? If you don’t mind, please tell us

    • @wadehuffaker9327
      @wadehuffaker9327 3 місяці тому

      @@milaloeb977 About four years ago I was starting to rapidly decline,, things were getting worse,, more symptoms started to appear. One of those symptoms was my appetite,, I was hungry all the time. So I researched for appetite suppressants,, found the oldest suppressant,, Nicotine. Did research on pure nicotine,, amazed at all the health benefits and found that it had been studied for use on Parkinson's. Started using nicotine patches,, the results were amazing! Not only did my appetite improve,, a lot of my other symptoms either improved or completely went away. The nicotine patches were expensive and would irritate my skin,, so I switched to using the nicotine pouches you put between your cheek and gum (Product names: Zyn, Velo, On, Lucy, Rogue, ect.) and still occasionally use the patches for muscle tightness. About six months later I started getting a resting tremor in my left hand. Did more research. Started taking low dose Methylene Blue. Haven't had a tremor since. I also (carefully) use Glutathione,, high dose vitamin B1 and other various supplements and I'm also on the carnivore diet.

    • @wadehuffaker9327
      @wadehuffaker9327 3 місяці тому

      @@milaloeb977 Tried to respond,, UA-cam removed my reply,, don't know why.