Jenna’s Lyme Video Blog

Jenna’s Lyme Video Blog

Video blog about chronic and/or neuro-Lyme

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Lyme Disease/CFIDS/ME and My Life Part One

Carrigon asked:


This is a two part video that describes how severely Advanced Lyme Disease and Chronic Fatigue Immune Dysfunction Syndrome affect my life. Also known as CFIDS/ME for Myalgic Encephalomyelitis.

Bethany

4 Responses to “Lyme Disease/CFIDS/ME and My Life Part One”

  1. 1
    OctaviaW:

    Annemarie

    CFIDS & Sims – what more could I want. Subbed:)

  2. 2
    THansen2009:

    Anne

    Thanks for sharing your story! My symptoms aren’t as severe but I can relate to so much of what you’ve said. It takes me a week or more to do what I used to do in a day. Keep up the fight!

  3. 3
    fogggygyrl:

    Cam

    Hi Tea,
    I know what you mean about having to choose what we do, it’s very hard living this way.

  4. 4
    justter:

    Christopher

    Carri! I’m SO glad to finally be able to see you! This is such a wonderfully informative video! You’ve been able to include so much of what I and others “forget” to talk about. I always tell people that I feel like I’m at least 80. On to the next vid.

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