Steve J.
Well known member
In June/July of 2015 I thought that I had this thang behind me. Now I'm going through hell again and I don't know what to do. I hadn't posted on the wiki for almost a year because I was so confident that my remission was complete.
I sent this message to Alan Gordon, but he has yet to respond. I'm wondering what kind of feedback some of you would be willing to provide:
How are you? I'm sure that you don't remember me, but we had a phone chat almost two years ago now in which you offered me great comfort and support that what I have is more than likely TMS. I then went on to have sessions with Alex Bloom for several months, but I wasn't really improving, and in March of 2015 I went to the hospital (voluntarily) for having suicidal thoughts that were not going away. After that, I went on anti-depressants and attended CBT for a while. By summertime I was feeling much, much better.
A brief recap of my history/symptoms:
Eczema as a child, and even occasionally now on my right pinky finger. (I'm now 26).
2010: OCD/anxiety/depression as I was studying abroad in Spain.
2011: 1+ year of unexplained abdominal pains/diarrhea (I saw two gastroenterologists, had stool samples taken, blood work done, a colonoscopy, in addition to seeing a urologist who performed a cystoscopy). I also had a renal sonogram performed. All came back perfectly fine/inconclusive. Eventually, the pain sort of just went away. It just did.
2011-2012: Officially diagnosed with intrusive thought OCD. This, I thought, would be the end of me. I was an absolute disaster. I was waking up every morning having these deeply unpleasant and disturbing thoughts that I was a sexual predator. Very intense. Very scary. I did not know what was going on with me, but eventually upon doing some research I realized it was all anxiety related. Upon the recommendation of my very supportive girlfriend at the time, I started doing CBT, and greatly improved.
March 2013: Injured my left wrist playing golf. The pain was not dissipating. Diagnosed with tendonitis by orthopedists. I had injections done, MRI's/x-rays taken, all came back fine. Eventually all the limbs in my body began to hurt. I had multiple MRI's done, bloodwork taken (rheumatoid factor), visited a neurologist who performed a brain/neck MRI, in addition to an EMG and nerve conduction tests. Some slightly low D and B12 levels so I started supplementation, but other than that all was fine. The pain was not diminishing.
2014: I was muddling through with the pain and discomfort. It wasn't easy, but I somehow managed. I ended up seeing an acupuncturist for about two months really to no avail. Tried going gluten free, etc, etc. I discovered TMS in November of 2014 while I was having low back pain in addition to limb pain. (I was seeing a chiropractor at the time. He wanted me to study dianetics. I got the hell out of there). My pain in my back and mostly arms at this point had taken over my life.
2015 came and I decided to go to see my primary physician (she is actually an NP) who had bloodwork taken, with equivocal/inconclusive results. I was diagnosed and conventionally treated for an anxiety disorder (my initial paragraph outlines that experience).
As I improved during that summer, I started doing all that I wanted to do again--playing basketball/football/baseball. I was feeling great. I thought I had it all licked. At the end of the summer, while skateboarding, I broke my right ankle. This started me worrying about pain again.
Fast forward until now. My arms and legs are in constant, round-the-clock pain. I have convinced myself that I have rheumatoid arthritis, even though I have zero swelling, and zero joint stiffness. My joints are pain-free, it is the muscles in the surrounding musculature that is clearly the issue--fibromyalgia-like symptoms, I would say. I get scared that it will take years to get a proper diagnosis. Anyway, my health anxiety/OCD has ramped up since I work as a server in a restaurant (I am a full-time student as well), and I worry that I won't be able to support myself as I continue my academics. I had to go back to my primary, and am taking anti-depressants again in addition to seeing my CBT therapist. I just had more blood work done yesterday--CBC, TIBC, RF, thyroid, Vitamin D. My primary is very confident that my biggest issue is depression/anxiety, and that those are the culprits behind my pain and discomfort.
I am very familiar with the TMS theory. I've read all of Sarno's books at least once, and read Steve O's book three times. I also have Dr. Schubiner's workbook. But I can't shake the idea that I have TMS...AND some sort of autoimmune disease. So obviously any work/reading that I put into this will really be futile if my belief is not 100%. My question is this: do you think at this point I should see a TMS physician? I'm so scared that I will see one and will have my biggest fears confirmed: that I am sick with an irreversible/uncurable illness. I don't understand how TMS could cause this much intense pain. I feel like it's worse than ever....
I'm sorry for going on and on. I feel like this message was almost a way for me to try convince myself of TMS again because I am seriously doubting it so much this time around, and I know how crucial acceptance of the diagnosis is. If I do see a TMS doctor, I'm thinking Paul Gwozdz since he's not terribly far away from me, and I hear great things.
Thank you for taking the time to read this mess.
Best,
Steve
I sent this message to Alan Gordon, but he has yet to respond. I'm wondering what kind of feedback some of you would be willing to provide:
How are you? I'm sure that you don't remember me, but we had a phone chat almost two years ago now in which you offered me great comfort and support that what I have is more than likely TMS. I then went on to have sessions with Alex Bloom for several months, but I wasn't really improving, and in March of 2015 I went to the hospital (voluntarily) for having suicidal thoughts that were not going away. After that, I went on anti-depressants and attended CBT for a while. By summertime I was feeling much, much better.
A brief recap of my history/symptoms:
Eczema as a child, and even occasionally now on my right pinky finger. (I'm now 26).
2010: OCD/anxiety/depression as I was studying abroad in Spain.
2011: 1+ year of unexplained abdominal pains/diarrhea (I saw two gastroenterologists, had stool samples taken, blood work done, a colonoscopy, in addition to seeing a urologist who performed a cystoscopy). I also had a renal sonogram performed. All came back perfectly fine/inconclusive. Eventually, the pain sort of just went away. It just did.
2011-2012: Officially diagnosed with intrusive thought OCD. This, I thought, would be the end of me. I was an absolute disaster. I was waking up every morning having these deeply unpleasant and disturbing thoughts that I was a sexual predator. Very intense. Very scary. I did not know what was going on with me, but eventually upon doing some research I realized it was all anxiety related. Upon the recommendation of my very supportive girlfriend at the time, I started doing CBT, and greatly improved.
March 2013: Injured my left wrist playing golf. The pain was not dissipating. Diagnosed with tendonitis by orthopedists. I had injections done, MRI's/x-rays taken, all came back fine. Eventually all the limbs in my body began to hurt. I had multiple MRI's done, bloodwork taken (rheumatoid factor), visited a neurologist who performed a brain/neck MRI, in addition to an EMG and nerve conduction tests. Some slightly low D and B12 levels so I started supplementation, but other than that all was fine. The pain was not diminishing.
2014: I was muddling through with the pain and discomfort. It wasn't easy, but I somehow managed. I ended up seeing an acupuncturist for about two months really to no avail. Tried going gluten free, etc, etc. I discovered TMS in November of 2014 while I was having low back pain in addition to limb pain. (I was seeing a chiropractor at the time. He wanted me to study dianetics. I got the hell out of there). My pain in my back and mostly arms at this point had taken over my life.
2015 came and I decided to go to see my primary physician (she is actually an NP) who had bloodwork taken, with equivocal/inconclusive results. I was diagnosed and conventionally treated for an anxiety disorder (my initial paragraph outlines that experience).
As I improved during that summer, I started doing all that I wanted to do again--playing basketball/football/baseball. I was feeling great. I thought I had it all licked. At the end of the summer, while skateboarding, I broke my right ankle. This started me worrying about pain again.
Fast forward until now. My arms and legs are in constant, round-the-clock pain. I have convinced myself that I have rheumatoid arthritis, even though I have zero swelling, and zero joint stiffness. My joints are pain-free, it is the muscles in the surrounding musculature that is clearly the issue--fibromyalgia-like symptoms, I would say. I get scared that it will take years to get a proper diagnosis. Anyway, my health anxiety/OCD has ramped up since I work as a server in a restaurant (I am a full-time student as well), and I worry that I won't be able to support myself as I continue my academics. I had to go back to my primary, and am taking anti-depressants again in addition to seeing my CBT therapist. I just had more blood work done yesterday--CBC, TIBC, RF, thyroid, Vitamin D. My primary is very confident that my biggest issue is depression/anxiety, and that those are the culprits behind my pain and discomfort.
I am very familiar with the TMS theory. I've read all of Sarno's books at least once, and read Steve O's book three times. I also have Dr. Schubiner's workbook. But I can't shake the idea that I have TMS...AND some sort of autoimmune disease. So obviously any work/reading that I put into this will really be futile if my belief is not 100%. My question is this: do you think at this point I should see a TMS physician? I'm so scared that I will see one and will have my biggest fears confirmed: that I am sick with an irreversible/uncurable illness. I don't understand how TMS could cause this much intense pain. I feel like it's worse than ever....
I'm sorry for going on and on. I feel like this message was almost a way for me to try convince myself of TMS again because I am seriously doubting it so much this time around, and I know how crucial acceptance of the diagnosis is. If I do see a TMS doctor, I'm thinking Paul Gwozdz since he's not terribly far away from me, and I hear great things.
Thank you for taking the time to read this mess.
Best,
Steve
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