Hello All:

I'm upset, and I would appreciate anyone's input... My story is long, but I will try to make it as brief as possible.

I am a long time TOS sufferer. I've had it for years and didn't know what it was. It originates from repetitive strain and carrying heavy bags on my shoulder.

A year ago last March, I started having symptoms in my opposite hand and arm. After seeing many specialists who could not diagnose me, a chiropractor talked to me about TOS. It fit. I had every symptom. I tried to eliminate my symptoms through stretching and exercise, but didn't have any luck. I needed to get back to work and decided to see a specialist in Denver.

Shortly before my trip to Denver, I started having numbness in my feet. When I arrived in Denver, I asked the doctor about it. He said it was not related to TOS. He confirmed I did have bilateral TOS. The scalene block eliminated all of the pain and tightness in the neck, shoulder, jaw, all the way to my hand.

He recommeded both surgeries (pec minor release and scalenectomy). I opted to have the pec minor surgery on both arms. I had good results from the surgery. The numbness and pain in both arms and hands went away. I still had some discomfort in the shoulder and neck area, as I was told I would.

I was able to land a short contract job a few weeks later. Up to this point, I felt good. The numbness in my feet also went away. Within a day or two of starting the contract job, the pain was back. My neck and shoulders were so stiff with pain, I could hardly move. I decided to have the scalenectomy.

I had the surgery. There were no complications. I was pretty much out of it for three weeks, and I was told this would be normal. After the fourth or fifth week, I decided to go back to my GP. The numbness and pain in my feet was working it's way north to my knees. In addition, I felt like I was coming down with something. I know this is foolish, but I had hoped the numbness and pain in my feet would go away with this surgery. I know that there have been others who had TOS and also had numbness in their feet.

At any rate, my GP said I probably had a neuropathy of some sort and prescribed Neurontin. It helped some, and I felt like I was recovering.

Over the next several months, I tried making lifestyle changes like eating better and exercising. I had developed severe migraines in an area that I never had headaches before, felt fatgued, and just poorly in general. This resulted is a couple of trips to the GP. They ordered tests for hypothyroidism and general lab work.

A few more months go by, and I get more symptoms. I notice the pain from the neuropathy is considerably worse just before and during that time of the month. It was also spreading. I have insomnia, short periods of nausea, problems with my vision, problems with memory and congnition, persistent sore throat, and depression. I think I possibly have fibromyalgia or CFS. I return to my GP. I was told no, I don't have the tender points for FM, and CFS generally comes on all at once, not gradually.

At this point, I ask for a referral to a neurologist. I knew the above symptoms I was having were not related to TOS or PN, but needed some relief from the PN. I go to a neuro. They order a MRI which comes back negative. He asks if I have been tested for lupus or diabetes. I wasn't sure if I was tested for lupus, but I knew I did not have diabetes. So I go back to my GP to request a test for lupus.

My normal GP wasn't in that day, so I see the partner. He orders a lupus test in addition to general blood work. He said my case was puzzling. The office has a policy that you have to come in the office for test results. No results are given over the phone.

Here's where I start to get upset....

A week or so goes by, and I return to my GP to get the results of my blood tests. She seems somewhat frustrated with me. She said my tests were normal, and she really couldn't do anything else for me. I try to explain that I know something is wrong. I am not a hypochondriac. I am trying to get to the bottom of my health issue. I need to go back to work. This whole process is about to financially bankrupt me. As an after thought, she said she didn't order a test for Lyme's disease. She writes the orders and gives the paperwork to me. She said I should go to the specialists and let them figure it out, that I did not need to come back to the office. I take my paperwork to the front receptionist. The receptionist also repeats that I do not need to come back. I asked what about my test results. She said they would call me if the results were positive.

I found this odd. It was almost as if the dr. had written something on the paperwork to indicate to the receptionist to tell me not to come back. Later, I thought I was being paranoid and let it go.

A short time later, I receive a letter from the hospital in Denver where I had the surgery. They inform me I may have possibly been exposed to hepatitis c through a terminated employee. I live half way across the country, so I naturally hadn't heard anything about his. I did some research on the internet, and it turns out that allegedly a surgical tech put thousands of patients at risk by stealing pain killing medication, injecting it into herself and returning the used needle back to the tray knowing she had the hep c virus. They already had over a dozen people who had contracted the disease. The hospital requests a blood test to confirm.

I take the blood test. A week later, the lab calls me to inform me that there was a lab error, and I have to retake the test. At this point, I'm a little concerned. I know the chances are slight, but still there is a chance, and I have not been right since the surgery. I call Denver and find out that the time frame is likely three weeks after the test is taken. Since I'm half way across the country, I figured three weeks plus a couple of days since I have to retake the test.

Even though my GP told me not to come back, I felt this was a new development. I also wanted to know if any of the blood work I had done over the last several months would indicate that I did not have the disease. I also thought that maybe they could order the tests and get the results sooner than three weeks, so I could have some peace of mind. The letter from the hospital recommends that I discuss the letter with my personal physician.

I call to make an appointment. I explain to the receptionist why I need to see the dr. A short time later, a nurse calls me explaining that there is nothing more the dr. can do for me, that I need to follow up with a specialist. I was so upset, I just hung up. I couldn't believe I was being treated this way.

I know that doctors are human and get frustrated with people. I know they have difficult patients. I thought maybe I was overreacting because I'm sick and tired of going to doctors and them telling me they can't find anything. I am also emotional because I can't work and I'm running out of money. Who will hire someone who has to be off for several days every month and can't concentrate on anything long enough to complete a project?

Anyway, I've vented long enough. I'm going again today to Quest to repeat my test for hep c, and I'll wait out the three weeks.