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Alan has completed the new Pain Recovery Program. To read or share it, use this updated link: https://www.tmswiki.org/forum/painrecovery/Dismiss Notice
Diana-M
Beloved Grand Eagle, Female, from East Coast, USA
Pain pathways are permanent but so are play pathways. Switching over…is the most powerful way to solve your pain. D. Hanscom, MD Jan 6, 2025 at 2:09 PM
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My Story
SHORT VERSION: I have been fighting TMS (and winning sometimes) on and off for 30 years. I discovered Sarno in 2017 and had a quick recovery. But in 2020, I broke out in multiple symptoms. And in March 2024, I joined this life-changing forum.
LONG VERSION:I have been fighting TMS on and off for 30 years. I have had insomnia, depression, IBS, foot pain, back pain, neck pain, severe panic attacks, leg numbness, neuropathy, burning legs, plantar fasciitis, leg weakness, allergies, asthma, persistent cough, numb and tingling hands, hands curling up (won’t open all the way, no gripping power), painful leg and stomach contractions, dizziness, electrical “buzzing” inside, sensitivities to things touching me, very cold feet, night terrors and balance issues.
In 2017, I discovered Dr. Sarno and immediately embraced TMS. I studied it day and night and started journaling about my emotions and got rid of tingling hands at the time. During my other episodes, I just somehow ignored it, and it went away eventually or diminished enough to live with it.
Flash forward to 2020. During the pandemic, I was extremely terrified, and under a great deal of stress on many levels. I began getting many new symptoms— plantar, foot pain, tingling, numbness, weakness, stiff knees, cramping hands, a feeling like strong hands are gripping my knees, or my hips.
Here’s more of my story if you’re interested: https://www.tmswiki.org/forum/threads/my-story-i-know-it%E2%80%99s-tms.28068/ (Day 1 - My story- I know it’s TMS) - Loading...
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My Story
- Gender:
- Female
- Location:
- East Coast, USA
SHORT VERSION: I have been fighting TMS (and winning sometimes) on and off for 30 years. I discovered Sarno in 2017 and had a quick recovery. But in 2020, I broke out in multiple symptoms. And in March 2024, I joined this life-changing forum.
LONG VERSION:I have been fighting TMS on and off for 30 years. I have had insomnia, depression, IBS, foot pain, back pain, neck pain, severe panic attacks, leg numbness, neuropathy, burning legs, plantar fasciitis, leg weakness, allergies, asthma, persistent cough, numb and tingling hands, hands curling up (won’t open all the way, no gripping power), painful leg and stomach contractions, dizziness, electrical “buzzing” inside, sensitivities to things touching me, very cold feet, night terrors and balance issues.
In 2017, I discovered Dr. Sarno and immediately embraced TMS. I studied it day and night and started journaling about my emotions and got rid of tingling hands at the time. During my other episodes, I just somehow ignored it, and it went away eventually or diminished enough to live with it.
Flash forward to 2020. During the pandemic, I was extremely terrified, and under a great deal of stress on many levels. I began getting many new symptoms— plantar, foot pain, tingling, numbness, weakness, stiff knees, cramping hands, a feeling like strong hands are gripping my knees, or my hips.
Here’s more of my story if you’re interested: https://www.tmswiki.org/forum/threads/my-story-i-know-it%E2%80%99s-tms.28068/ (Day 1 - My story- I know it’s TMS)Interact
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