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Michele

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@michele55

In April 2021 I was diagnosed with IPF, both my brother and father died as a result of Ipf, so when I was diagnosed I was not surprised. My question to the forum members is as follows: How many members have Dupuytren’s? I have watched my hands change over the last 6 months. I sometimes wonder if my hands are not acting as an indicator for the […] View
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    Jorge Ríos and Profile picture of MicheleMichele are now friends 1 year ago

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    Michele posted a new activity comment 1 year, 3 months ago

    Thank you for your reply. I have since since a Rheumatologist and they agree with you. No connection to ipf just a coincidence.

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    Michele replied to the topic Dupuytren's and Raynauds with IPF in the forum Living with Pulmonary Fibrosis: 50+ 1 year, 6 months ago

    After a long wait to see the Rheumatologist I cannot report any specific findings. Today was the day! At this time the doctor said that their is no, or not sufficient evidence to suggest scleroderma. Which is great news! But I am left with the questions of what my tendons in my hands are doing and planning to do? They are still troubling me and…[Read more]

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    Michele replied to the topic Dupuytren's and Raynauds with IPF in the forum Living with Pulmonary Fibrosis: 50+ 1 year, 7 months ago

    So we are not alone! I am due to see a Rheumatologist soon to look at this concern. I will let you know what I learn. For now I take anti inflammatory meds because the pain, difficulty and loss of my finger functions were making me feel a little desperate.

    Michele

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    Michele started the topic Dupuytren's and Raynauds with IPF in the forum Living with Pulmonary Fibrosis: 50+ 1 year, 7 months ago

    I have developed Dupuytren’s and Raynauds over the last 6 months. Sometimes I have aches in my fingers and palms and in my index finger shooting pain and numbness. (I know that sounds impossible but it happens) I was just wondering if anyone else has issues with their hands.

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    Michele replied to the topic Acute Exacerbation and Cyclophosphamide in the forum Living with Pulmonary Fibrosis: 50+ 1 year, 7 months ago

    Dear All

    I have read with interest the reports of low oxygen saturation after a covid jab. I had the Johnson & Johnson and for 24 hours afterwards I had low oxygen saturation. I clearly was not alone.

     

     

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    Michele replied to the topic Coughing in the forum Join the Discussion: Welcome to all PF/IPF Patients 1 year, 8 months ago

    Omez 40mg once a day before food sorted me out. I hope everyone can access it. It works.

  • Profile picture of Michele

    Michele posted an update 1 year, 8 months ago

    In April 2021 I was diagnosed with IPF, both my brother and father died as a result of Ipf, so when I was diagnosed I was not surprised.

    My question to the forum members is as follows: How many members have Dupuytren’s? I have watched my hands change over the last 6 months. I sometimes wonder if my hands are not acting as an indicator for the…[Read more]

  • Profile picture of Michele

    Michele joined the group Group logo of Research and DevelopmentResearch and Development 1 year, 8 months ago

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    Michele became a registered member 1 year, 9 months ago

    • Profile picture of Charlene Marshall
      Charlene Marshall replied 1 year, 9 months ago

      Thanks for joining the PF forums Michele. Welcome!

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This site is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

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