Washingtonians

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I was diagnosed in late 2005, when my son was less than a year old. I think either the birth (which was a c/s) or the following sleep deprivation set it off. I had pain in my elbows and hips that wouldn't go away. It was the elbow pain that sent me to the doctor; they thought I had tendinitis and wanted to inject cortisone. Finally, one sent me to a rheumatologist instead. I think, as FMS cases go, mine is not too severe. My biggest symptom is fatigue, followed by a general achiness/tension that I sometimes wonder if a long hot soak or the right massage would fix (not that I've ever been able to try).

I'm of the impression that FMS pain is *not* caused by inflammation. Am I mixing that up?

I think that every case of Fiobro is different just like every person is so I can only tell you about mine. I was diagnosed in 1994. After many kinds of treatment from different Dr's I turned to alternative med. they told me that if I was allergic to certain foods it would cause inflammation internaly like hay fever makes your eyes itch and you sneeze. I did allergy testing with them, found I was allergic to alot of foods, went on a diet that used only foods that I did not normally eat,and was not allergic to. Did this for about 6 months. then I could start to add back but only very rarely one ,at a time,those that I showed reaction to. I worked for me! Now I can tell the next day if I have eaten someting I should not, painful stiff joints, fever, poor vision, mind fog and (poor spelling) I have fallen and broken both ankles at the same time-don't ever do that- and now both wrists. I have been having a terrible time since I broke my left wrist in July and had to have a SSteel plate put in, I am begining to wonder if the plate is causeing some kind of "inflamation itself".I also have RA and secondary sjogrens syndrome. Autoimune
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Thanks CL!
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I have an MRI and ultrasound next week. They found spots on the left now as well as the right so they want to get a better look at both. Good grief! Bout ready to say ta ta to the ta-tas!
Sorry for the sad sense of humor but it might be kind of fun to pick a new size! Wonder if they can do a tummy tuck at the same time? The twins kind of did me in!
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Quote:
Thanks CL!
hugs.gif

I have an MRI and ultrasound next week. They found spots on the left now as well as the right so they want to get a better look at both. Good grief! Bout ready to say ta ta to the ta-tas!
Sorry for the sad sense of humor but it might be kind of fun to pick a new size! Wonder if they can do a tummy tuck at the same time? The twins kind of did me in!
tongue.png


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Good Attitude!
 
Quote:
Thanks CL!
hugs.gif

I have an MRI and ultrasound next week. They found spots on the left now as well as the right so they want to get a better look at both. Good grief! Bout ready to say ta ta to the ta-tas!
Sorry for the sad sense of humor but it might be kind of fun to pick a new size! Wonder if they can do a tummy tuck at the same time? The twins kind of did me in!
tongue.png


thumbsup.gif
Good Attitude!

X2 I try to be very careful but find some humor helps. I guess It is one of the few good things I got from my dad. See when he was doinf radiation they would do x-rays. Well seems dad also had a bit of a twisted sense of humor. Once he had me help him sneak a bullet in under his head just before the x-ray. There was some brie freaking out panic.
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It wa sso worth itto see the lok on thier faces.. Some times ya just gotta find a way to make thebest of things.

OK been up since just beore 3:00 am and it is now 31*. I am gonna feed da dragon and get horizointaly so I can count my chicks before they hach.
 
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That Stinks. You might want to switch majors.

When I attended UC Davis a few decades ago, I switched my major at the end so I could graduate sooner, otherwise I would have had to wait more than a year for a class that was only offered in Spring quarters of alternating years! I had to take 5 more classes to switch majors, but I got them all in the next 2 quarters. I did have to do the 5th year senior as they did not accept any of my chemistry classes, physiology and anatomy from the JC, but I did get them to accept all my biology (same book taught in 1 year - a much better and thorough class than the way it was taught at Davis - Entire Hickman book crammed into 1 quarter. The instructors hated when they were made to reduce the class to 1 quarter and were gladd I had all my notes and assignments to show how much better the class was taught at the J.C. where they had time to teach it properly.)

Good luck getting them to accept your classes! In some ways I wish I had stayed longer as I enjoyed college far more than my career!
 
Quote:
I was diagnosed in late 2005, when my son was less than a year old. I think either the birth (which was a c/s) or the following sleep deprivation set it off. I had pain in my elbows and hips that wouldn't go away. It was the elbow pain that sent me to the doctor; they thought I had tendinitis and wanted to inject cortisone. Finally, one sent me to a rheumatologist instead. I think, as FMS cases go, mine is not too severe. My biggest symptom is fatigue, followed by a general achiness/tension that I sometimes wonder if a long hot soak or the right massage would fix (not that I've ever been able to try).

I'm of the impression that FMS pain is *not* caused by inflammation. Am I mixing that up?

I think that every case of Fiobro is different just like every person is so I can only tell you about mine. I was diagnosed in 1994. After many kinds of treatment from different Dr's I turned to alternative med. they told me that if I was allergic to certain foods it would cause inflammation internaly like hay fever makes your eyes itch and you sneeze. I did allergy testing with them, found I was allergic to alot of foods, went on a diet that used only foods that I did not normally eat,and was not allergic to. Did this for about 6 months. then I could start to add back but only very rarely one ,at a time,those that I showed reaction to. I worked for me! Now I can tell the next day if I have eaten someting I should not, painful stiff joints, fever, poor vision, mind fog and (poor spelling) I have fallen and broken both ankles at the same time-don't ever do that- and now both wrists. I have been having a terrible time since I broke my left wrist in July and had to have a SSteel plate put in, I am begining to wonder if the plate is causeing some kind of "inflamation itself".I also have RA and secondary sjogrens syndrome. Autoimune
tongue.gif


My Fibro isn't inflammatory, so I don't get any relief from ant-inflammatory drugs for the Fibro pain. What is going on with my hips seems to have another cause, because I know that it is inflammation. I was also was told that Fibro isn't progressive, and I am now sure that isn't true. Things have gotten much worse over the years. I do agree that it does have a rather wide variety of symptoms, and that it can be different for everyone. I think that the diagnosis of Fibro has become a dumping ground for doctors that don't know what is wrong with us. It's become a kind of catch all diagnosis. There are a number of new meds for treating Fibro, but the side effects can be just plain dangerous. I have always had problems taking antidepressants. It is automatically assumed that if you have Fibro then you must be depressed. I don't agree, at times I can be sad and depressed that I am in pain all the time, but most of the time I have things to do people to see, and plans I want to accomplish. I know that I don't have only one feeling. I know this will not harm me or kill me. It is simply the way it is for me. It's kind of like missing a limb, you have to learn to adapt to the way your body works now. It can really suck elves some days, but it isn't the worst thing that can happen to you.
 
Well I am going to the movies tomorrow with my DMiL, and since it starts at 12:30pm, I am going to need to get up earlier than normal. At least I got all the nasty little dogs scrubbed up tonight. Miss Gabby was stinky, and didn't even offer to argue with me. Teddy on the other hand was trying hard to not have the bath and still get the treat. I am a very mean dog mama. No bath = No treat.
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