Polymyositis: Understanding the Rare Autoimmune Disease

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  • เผยแพร่เมื่อ 15 ต.ค. 2024

ความคิดเห็น • 35

  • @christopherfothergil
    @christopherfothergil 5 หลายเดือนก่อน +6

    I had this illness here in the UK and my wife was warned i may not survive the disease. It was a Greek doctor in my hospital who found out the cause which was a allergic reaction to Citalopram anti depressive drug. I went from hill walking and driving to only being able to crawl on all fours and finally in a wheelchair almost death within two weeks. My wife was told to prepare for the worst. I was treated by high doses of prednisone steroid drugs and the change of anti depressant drugs. I was told 60% of my muscle mass was destroyed. yes as soon as i changed the Citalopram and placed on steroids with three days I left the hospital very weak but feeling a lot better.

    • @MedicalCentric
      @MedicalCentric  5 หลายเดือนก่อน +2

      I'm deeply relieved to hear about your recovery and commend the astute medical attention you received. Wishing you continued strength and health.

    • @apacur
      @apacur 2 หลายเดือนก่อน

      How are you now?

    • @christopherfothergil
      @christopherfothergil 2 หลายเดือนก่อน +2

      @@apacur it took four years to get back the muscle mass i lost. But i am now fully fit, thanks you

    • @apacur
      @apacur 2 หลายเดือนก่อน

      @@christopherfothergil What worked- as far as regaining the muscle mass?

    • @christopherfothergil
      @christopherfothergil 2 หลายเดือนก่อน +2

      @@apacur i was put onto a very high dose of Prednisalone. I had a very high dose. My specialist said it was going to be a long process to get back to full fitness.

  • @toolfoolmostrom6254
    @toolfoolmostrom6254 หลายเดือนก่อน

    My rheumatologist diagnosed me with this last month, she found it in my bloodwork

    • @MedicalCentric
      @MedicalCentric  หลายเดือนก่อน

      @toolfoolmostrom6254 It sounds like your rheumatologist identified something important through your bloodwork. Autoimmune conditions or inflammatory markers are often detected this way, and it's great that your doctor caught it. Make sure to follow up on the treatment plan and ask any questions you might have about managing your condition. You're on the right track to understanding your health better-stay strong! 😊

    • @toolfoolmostrom6254
      @toolfoolmostrom6254 หลายเดือนก่อน

      @@MedicalCentric it took me 10 years to get a diagnosis, but they were kinda stuck on my spine and neck being the culprit because of some injuries and degenerative disc disease. But that shouldn’t make my joints hurt like they do so I’m glad I finally found a doctor that actually listened to my symptoms and found an answer.

  • @LadyKestrel23
    @LadyKestrel23 หลายเดือนก่อน

    Is this easy to test for? I read that blood tests can two if you have inflammation and muscle enzymes?

    • @MedicalCentric
      @MedicalCentric  หลายเดือนก่อน +1

      @LadyKestrel23 Yes, blood tests can help in diagnosing conditions related to inflammation and muscle health. Tests can measure various markers, including:
      - **Inflammatory Markers**: Such as C-reactive protein (CRP) or erythrocyte sedimentation rate (ESR), which can indicate inflammation in the body.
      - **Muscle Enzymes**: Elevated levels of enzymes like creatine kinase (CK) can signal muscle damage or inflammation.
      These tests can provide valuable information to help diagnose underlying conditions. However, a comprehensive evaluation by a healthcare provider, including a review of symptoms and medical history, is essential for accurate diagnosis and treatment.

    • @LadyKestrel23
      @LadyKestrel23 หลายเดือนก่อน

      @@MedicalCentric thank you so much! I really appreciate your help! 🧡🧡

  • @elfrancoterador1961
    @elfrancoterador1961 ปีที่แล้ว +3

    Present 👋

    • @waelfadlallah8939
      @waelfadlallah8939 ปีที่แล้ว +2

      U always are

    • @elfrancoterador1961
      @elfrancoterador1961 ปีที่แล้ว

      @@waelfadlallah8939 شكرا وائل فضل الله shukraan and i always will be😊👋

    • @waelfadlallah8939
      @waelfadlallah8939 ปีที่แล้ว +1

      @@elfrancoterador1961 good spelling 👍and you're welcome :)

    • @elfrancoterador1961
      @elfrancoterador1961 ปีที่แล้ว +1

      @@waelfadlallah8939 thanks alot.. actually im arab... from arab country what about you?

    • @waelfadlallah8939
      @waelfadlallah8939 ปีที่แล้ว +1

      @@elfrancoterador1961 same, from lebanon.

  • @TheMerdy1
    @TheMerdy1 11 หลายเดือนก่อน +1

    My mother has polymyositis for about year and a half. Shes 59, it all started almost 2 years after she lost her brother, could it be the starter? she also started smoking from that time...
    She had prednisone prescribed, and after a year she finally feels better. Is it possible to get rid of Polymyositis? To be fully cured?

    • @MedicalCentric
      @MedicalCentric  11 หลายเดือนก่อน

      Here are some general insights. Polymyositis is a complex autoimmune condition, and its exact cause is not well understood. It's unlikely that the loss of her brother directly triggered the condition, but stress and lifestyle changes could contribute to its development or exacerbation. Smoking is generally not recommended for individuals with autoimmune conditions, as it can worsen symptoms. Prednisone and other medications are typically used to manage symptoms and control inflammation, but achieving a full cure for polymyositis is challenging. Consult with a healthcare provider for the most accurate assessment of her condition and prognosis.

    • @TheMerdy1
      @TheMerdy1 11 หลายเดือนก่อน +1

      Thank you very much for the answer. So I understand it like this - your own T lymphocytes start to attack your own cells especially muscle tissues. Thats basically polymyositis? And the question is that now, after 2 years, although she feels better, if that T lymphocytes still do the same, or her immunity is basically back to normal, and the disease just vanished like covid or flu and it might comeback at anytime (age, smoking, stress etc.)@@MedicalCentric

  • @E-commerce-galaxy
    @E-commerce-galaxy 3 หลายเดือนก่อน

    Does it effect life expectancy?

    • @MedicalCentric
      @MedicalCentric  3 หลายเดือนก่อน

      Polymyositis can affect life expectancy, particularly if complications like respiratory or cardiac issues arise, but with early diagnosis and proper treatment, many patients manage well ❤️.

    • @christopherfothergil
      @christopherfothergil 2 หลายเดือนก่อน

      your life is fine

  • @neetashukla5092
    @neetashukla5092 ปีที่แล้ว

    Muje darmeto mayosytis h upay bataye please

  • @ApostolosKatsioulas
    @ApostolosKatsioulas 11 หลายเดือนก่อน +2

    I must be infected with polymyositis, both my legs ache badly; it's hard to walk, it's hard to perform lunges, it's hard to lay down. It's been at least one month that this has been happening. I am scared to death and I have no idea how long the treatment is going to last.

    • @MedicalCentric
      @MedicalCentric  11 หลายเดือนก่อน +1

      Polymyositis is a rare inflammatory disease that affects the muscles, causing muscle weakness, pain, and fatigue. If you're experiencing persistent muscle pain and difficulty walking, it's essential to consult a healthcare professional as soon as possible. They can perform a thorough evaluation to determine the cause of your symptoms and develop an appropriate treatment plan. While I can't offer a specific timeline for treatment, early diagnosis and treatment can lead to better outcomes. Remember, it's natural to be concerned, but medical intervention is crucial for addressing your symptoms and providing you with the best possible care. Please reach out to a healthcare provider to discuss your condition and receive the appropriate guidance and treatment.

    • @bluewave7120
      @bluewave7120 10 หลายเดือนก่อน

      Don't panic although possible your symptoms are more likely a less severe diagnosis The human body has very few ways to react to a wide variety of illnesses