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Mishwell
Last Activity:
Jun 30, 2023
Joined:
May 30, 2023
Messages:
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0
Trophy Points:
3
Gender:
Female
Location:
Australia
Occupation:
Musician/Homeduties

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Mishwell

Newcomer, Female, from Australia

How do I communicate with people on this site. It really isn’t obvious? Jun 1, 2023

Mishwell was last seen:
Jun 30, 2023
  • My Story

    I’ve really had TMS Avery long time.
    Years ago I spent thousands trying to find the answers to my symptoms. I felt twisted, all wrong. I can’t recall my diagnosis back then but they weren’t structural, just normal wear and tear for my age at the time.
    Finally I found Dr Sarno’s work and as a result of his approach I’ve overcome the chronic back issues.
    However TMS has octopussed its way into the facade of several other sensations including finger pain, knee burning, buttock pain, costacondroitus (heart area pain) burning under right rib cage, breast pain, elbow and wrist pain, general achiness. After the last back spasm 18 months ago the back pain subsided relatively quickly but suddenly my right hip/thigh/groin became so pained I couldn’t walk without pain or perform any leg movement sideways without pain. This went on for about 12 months.
    It recently subsided but these sensations (like my leg is going yo snap off at the hip) has migrated into the left hip/thigh/groin. I cannot shake it this time. It gets me so down.
    I don’t want to get more diagnosis’s as if it’s arthritis, there’s no cure. Given that I am and A student when it comes yo having the traits of a typical TMS candidate (I have them all) I just know it’s TMS.
    I have joined the Curable community and am doing more ‘work’. Where I’m at now emotionally is that I’m aware there are a million reasons why my brain is feeling unsafe, and I know it’s my job yo self soothe, however I need support from similar sufferers, I’m so alone and feel so stuck, literally in my life and in my leg.
    I feelthat my being isolated is what’s preventing my recovery. There are no TMS type therapists in my region.
    1. Mishwell
      Mishwell
      How do I communicate with people on this site. It really isn’t obvious?
      1. RobOptimist
        RobOptimist
        Hi, you probably want to "Post New Thread" in the appropriate subforum, for instance Support Subforum.
        Jun 2, 2023
        Cap'n Spanky likes this.
    2. Mishwell
      Mishwell
      I’ve recovered myself from 20yrs back pain, masqueraded over the years as several other symptoms. Now it’s debilitating roving hip pain.
    3. Mishwell
      Mishwell
      Hey peeps I’m new here kinda. X
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  • My Story

    Gender:
    Female
    Location:
    Australia
    Occupation:
    Musician/Homeduties
    Diagnoses:
    Hip joint/inner thigh tightness/pain on walking - sometimes.
    I’ve really had TMS Avery long time.
    Years ago I spent thousands trying to find the answers to my symptoms. I felt twisted, all wrong. I can’t recall my diagnosis back then but they weren’t structural, just normal wear and tear for my age at the time.
    Finally I found Dr Sarno’s work and as a result of his approach I’ve overcome the chronic back issues.
    However TMS has octopussed its way into the facade of several other sensations including finger pain, knee burning, buttock pain, costacondroitus (heart area pain) burning under right rib cage, breast pain, elbow and wrist pain, general achiness. After the last back spasm 18 months ago the back pain subsided relatively quickly but suddenly my right hip/thigh/groin became so pained I couldn’t walk without pain or perform any leg movement sideways without pain. This went on for about 12 months.
    It recently subsided but these sensations (like my leg is going yo snap off at the hip) has migrated into the left hip/thigh/groin. I cannot shake it this time. It gets me so down.
    I don’t want to get more diagnosis’s as if it’s arthritis, there’s no cure. Given that I am and A student when it comes yo having the traits of a typical TMS candidate (I have them all) I just know it’s TMS.
    I have joined the Curable community and am doing more ‘work’. Where I’m at now emotionally is that I’m aware there are a million reasons why my brain is feeling unsafe, and I know it’s my job yo self soothe, however I need support from similar sufferers, I’m so alone and feel so stuck, literally in my life and in my leg.
    I feelthat my being isolated is what’s preventing my recovery. There are no TMS type therapists in my region.