KatieDid123
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Question
Hi,
My TMS mostly manifests as pain in my right foot and ankle, which I've had for about 3 years following an injury. I found out about TMS about a year and half ago and went to see Dr. Schechter who diagnosed me as a clear-cut TMS case. Since then, I've had ups and downs with the pain, and I believe the reason it hasn't completely resolved is because I don't believe it 100%. While the pain used to only be in my one foot, it's now in my right buttock, left shoulder blade area, left arm, and sometimes upper back and neck. I told a family friend about my widespread pain and she urged me to get checked for Lyme disease. I went to a Lyme specialist and got bloodwork done from a specialty lab in CA called Igenex. My results came back negative according to the CDC's guidelines, but positive according to Igenex's guidelines. Lyme doctors claim that the CDC's guidelines are too lax and miss the majority of cases. I used to have extreme fatigue, brain fog, etc. too, which further supported the Lyme diagnosis, although these symptoms (fatigue, fog) have largely resolved.
My question is, what are your thoughts about Lyme in regards to TMS? I know Sarno mentions it in The Mindbody Prescription. I understand that Lyme is a real disease that can affect a person, but the symptoms are usually sudden and obvious (ie. rash, headache, fever, etc.) and are resolved with a course of antibiotics. Lyme doctors claim that if you're infected, but don't get treatment, the Lyme can become chronic and cause problems for you down the line. This is a roadblock for me, in that I'm worrying that I might actually have Lyme, which could be the cause of all my pain. On the other hand, I don't recall an acute phase of the disease where I got suddenly sick. I also didn't see a rash (but this doesn't occur in all people). According to Lyme docs, the symptoms are extremely broad and seem to include literally every possible physical symptom someone could have. These broad symptoms make for a go-to diagnosis for doctors to give if they can't find any other reasons for your pain. "Oh you're tired? It must be Lyme." "Oh you have ankle and shoulder pain? It must be Lyme." Kind of in the same vein as Fibromyalgia.
I just can't seem to get the positive Igenex test out of my head. It's preventing me from moving forward with TMS 100%. I understand you can't diagnose, but I'd love to hear any thoughts you have about chronic Lyme in relation to TMS.
Thank you,
Katie
My TMS mostly manifests as pain in my right foot and ankle, which I've had for about 3 years following an injury. I found out about TMS about a year and half ago and went to see Dr. Schechter who diagnosed me as a clear-cut TMS case. Since then, I've had ups and downs with the pain, and I believe the reason it hasn't completely resolved is because I don't believe it 100%. While the pain used to only be in my one foot, it's now in my right buttock, left shoulder blade area, left arm, and sometimes upper back and neck. I told a family friend about my widespread pain and she urged me to get checked for Lyme disease. I went to a Lyme specialist and got bloodwork done from a specialty lab in CA called Igenex. My results came back negative according to the CDC's guidelines, but positive according to Igenex's guidelines. Lyme doctors claim that the CDC's guidelines are too lax and miss the majority of cases. I used to have extreme fatigue, brain fog, etc. too, which further supported the Lyme diagnosis, although these symptoms (fatigue, fog) have largely resolved.
My question is, what are your thoughts about Lyme in regards to TMS? I know Sarno mentions it in The Mindbody Prescription. I understand that Lyme is a real disease that can affect a person, but the symptoms are usually sudden and obvious (ie. rash, headache, fever, etc.) and are resolved with a course of antibiotics. Lyme doctors claim that if you're infected, but don't get treatment, the Lyme can become chronic and cause problems for you down the line. This is a roadblock for me, in that I'm worrying that I might actually have Lyme, which could be the cause of all my pain. On the other hand, I don't recall an acute phase of the disease where I got suddenly sick. I also didn't see a rash (but this doesn't occur in all people). According to Lyme docs, the symptoms are extremely broad and seem to include literally every possible physical symptom someone could have. These broad symptoms make for a go-to diagnosis for doctors to give if they can't find any other reasons for your pain. "Oh you're tired? It must be Lyme." "Oh you have ankle and shoulder pain? It must be Lyme." Kind of in the same vein as Fibromyalgia.
I just can't seem to get the positive Igenex test out of my head. It's preventing me from moving forward with TMS 100%. I understand you can't diagnose, but I'd love to hear any thoughts you have about chronic Lyme in relation to TMS.
Thank you,
Katie
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