Crippling Pain? Try... Strenuous Exercise!

No more so than with an 'invisible disability' like mine, that causes chronic, relentless, breathtaking pain every second I'm awake - do you find out how incredibly rude and downright stupid some people in the medical profession are.

I am blessed but it took time and patience to find doctors willing to listen and help me. I was accused of doctor-shopping and put through the ringer by disability, but truth will out and I held my ground. I have a wonderful team now, though the loss of my therapist in February 2008 is irreplaceable.

My PCOS has been very bad since I gave birth almost 11 years ago. It's not getting any better and now I am having surgery sometime soon - again. Unfortunately the surgeries, medications and PCOS caused me to gain weight as well as look distended. I have lost some but I am more interested in sticking to a healthy diet I can live with.

But one thing I have always had a problem with: I don't do stupid. Stupidity really grates on me like nothing else. And as I get older, people around me seem to be getting stupider by leaps and bounds.


In reading one of my FAVORITE blogs, Shapely Prose - I came across a link to this blog: First, Do No Harm. I have it on my RSS Reader now. This post is spot-on about the absolute dumb things people like me have to deal with on an ongoing basis from the medical community.


~~~~~~~~
5 years ago, at 230 pounds, I decided to go on a diet. It started off typically: planned meals, calorie journal, joining the gym. Before long, I was restricting myself to no more than 500 calories a day, and exercising upwards of 3 hours a day, 7 days a week. I was biking, running, lifting, doing yoga. I dropped 70 lbs in 5 months. Down to 160 lbs and a size 12 from a 20.

At about the 6 month point, I started having all these aches and pains. First in my wrists, then my shoulders, then my hips. Pretty soon, I was in horrible pain all the time, all over my body.

I went to the doctor to check out what was wrong. I got around 10 seconds to describe my pain. Her response? “That’s what happens to people your size. You’re putting too much pressure on your joints. Try eating less, and start exercising.” We hadn’t talked at all about my food intake or exercise routine. She handed me a flier for an Overeaters Anonymous group that met at the hospital and showed me out of the room.

Flash forward 4 years.

By this time, I was in such pain, so stiff, so tired, I couldn’t exercise anymore. Many days I couldn’t even bathe myself, do basic household chores or go to work. The weight all came back, plus 30 lbs. I had to move home with my parents to have them care for me.

I’d seen dozens of doctors, had MRIs, CT Scans, XRays, every blood test available. Nothing ever showed up, so the only treatment I got was the suggestion to lose weight. And some mentions of gastric bypass.

I finally found a great nurse who realized that what was wrong was that I had fibromyalgia. The first step in the treatment plan was to see a physical therapist.

I showed up for the first appointment, and before asking me any questions about my health, the therapist said, “You know, 30 isn’t too young to have a heart attack. As big as you are, you really need to worry about that.” Without knowing any of my vital statistics, or asking me why I was there, she started laying out a plan that had me exercising 2+ hours a day, with the goal of dropping at least 100 pounds that year.

When I explained that I had FMS, and that light exercise was good, but too much exercise would actually cause a flare and make my symptoms worse, her response was:
“Well, you’re just going to have to deal with the pain until you get down to a normal size. The fibromyalgia will probably just go away then, anyway. I think most people who get diagnosed with that condition really just are too fat and too sedentary and want an excuse.”
Fortunately, at this point, I’d suffered enough, and knew my body well enough to know not to listen to her and find a new therapist. But if I hadn’t been as informed and willing to stand up to her, I can only imagine what damage she would have caused on my body.

SOURCE

Comments

I suffer from Fibromyalgia also and I am not overweight. Sometimes the pain is searing like hot electricity down my legs. But I feel as if I am coming down with the flu quite a lot.. but it has nothing to do with weight.
Hard exercise will just make it impossible for a fibro sufferer to move for days!
The medical profession has no clue what they are doing. I finally was given a book on fibromyalgia by a doctor who has it himself.. and what a relief.
Anonymous said…
we have a friend who suffers from fibromyalgia......

I cannot fathom why people don't take patients more seriously.

our parents are doctors and would never do such things......

apparently the Hippocratic Oath is seen as ancient history and some archaic mumbo jumbo by some people in the medical profession today

Ivan of athenivanidx
Rob at Kintropy said…
I came across your blog from Reimer Reason. Glad you've been able to work through the doctors & therapists critically (but sorry you had to do so).

Love the Barbie with the tallis, by the way - very cool.
Anonymous said…
I get migraines - I stopped going to the dr for them when I was asked if I wanted something for the pain or for the vomiting.

It made me wonder if he asks someone with a broken bone if they want the bone set or if they want something for the pain...
Anonymous said…
I was diagnosed with FM in Oct 08 by my primary. I did not beleive him ~ I thought he was just pusing me off with the , "okay, here's what's wrong with you" I went to a pain management specialist for a second opinion, however, when I made the pms aware of the FM diagnosis that was all he could focus on for the remainder of the appointment. He told me I need to seek phsycatic help and remove the stress from my life and I would get better. I was very discouraged and felt like I was possibly crazy and making this up? Although I've had this problem for 16 years. This week I decided to seek the advice of a different PMS recommended to my by my spinal surgeon, he was great as was his staff. He has started me on Cymbalta and a powerful stimulator. I am only on day 3 of the Cymbalta and have previously used the Tens Unit with success and can already tell a huge difference in the stimulator units. I have been pretty sick with the first 2 days of meds but I am very hopeful things will improve quickly. I tried Lyrica with no pain relief ~ only weight gain (quickly).

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