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Showing posts with label Letter to Doctor. Show all posts
Showing posts with label Letter to Doctor. Show all posts

WHAT YOU SHOULD KNOW ABOUT FIBROMYALGIA


ABOUT FIBROMYALGIAApr 30, '07 7:21 AM


 











  WHAT YOU SHOULD KNOW ABOUT FIBROMYALGIA

1. FMS is not the newest fad disease. In fact, it isn’t a disease at all, and it isn’t even new. In 1815, a surgeon at the University of Edenburgh, William Balfour, described fibromyalgia. Over the years, it has been known as chronic rheumatism, myalgia and fibrositis. Unlike diseases, syndromes do not have a known cause, but they do have a specific set of signs and symptoms which, unfortunately for the patient, take place together. Rheumatoid arthritis and lupus are also syndromes.

2. The many physical and emotional problems associated with FMS are not psychological in origin. This is not an “all in your head” disorder. In 1987, the American Medical Association recognized FMS as a true physical illness and major cause of disability.

3. Syndromes strike life-long athletes as viciously as they do couch potatoes. They can be disabling and depressing, interfering with even the simplest activities of daily life.

WHAT YOU SHOULD KNOW ABOUT ME
1. My pain - My pain is not your pain. It is not caused by inflammation. Taking your arthritis medication will not help me. I can not work my pain out or shake it off. It is not even a pain that stays put. Today it is in my shoulder, but tomorrow it may be in my foot or gone. My pain is believed to be caused by improper signals sent to the brain, possibly due to sleep disorders. It is not well understood, but it is real.

2. My fatigue - I am not merely tired. I am often in a severe state of exhaustion. I may want to participate in physical activities, but I can’t. Please do not take this personally. If you saw me shopping in the mall yesterday, but I can’t help you with yard work today, it isn’t because I don’t want to. I am, most likely, paying the price for stressing my muscles beyond their capability.

3. My forgetfulness - Those of us who suffer from it call it fibrofog. I may not remember your name, but I do remember you. I may not remember what I promised to do for you, even though you told me just seconds ago. My problem has nothing to do with my age but may be related to sleep deprivation. I do not have a selective memory. On some days, I just don’t have any short-term memory at all.

4. My clumsiness - If I step on your toes or run into you five times in a crowd, I am not purposely targeting you. I do not have the muscle control for that. If you are behind me on the stairs, please be patient. These days, I take life and stairwells one step at a time.

5. My sensitivities - I just can’t stand it! “It” could be any number of things: bright sunlight, loud or high-pitched noises, odors. FMS has been called the “aggravating everything disorder.” So don’t make me open the drapes or listen to your child scream. I really can’t stand it.

6. My intolerance - I can’t stand heat, either. Or humidity. If I am a man, I sweat…profusely. If I am a lady, I perspire. Both are equally embarrassing, so please don’t feel compelled to point this shortcoming out to me. I know. And don’t be surprised if I shake uncontrollably when it’s cold. I don’t tolerate cold, either. My internal thermostat is broken, and nobody knows how to fix it.

7. My depression - Yes, there are days when I would rather stay in bed or in the house or die. I have lost count of how many of Dr. Kevorkian’s patients suffered from FMS as well as other related illnesses. Severe, unrelenting pain can cause depression. Your sincere concern and understanding can pull me back from the brink. Your snide remarks can tip me over the edge.

8. My stress - My body does not handle stress well. If I have to give up my job, work part time, or handle my responsibilities from home, I’m not lazy. Everyday stresses make my symptoms worse and can incapacitate me completely.

9. My weight - I may be fat or I may be skinny. Either way, it is not by choice. My body is not your body. My appetite is broken, and nobody can tell me how to fix it.

10. My need for therapy - If I get a massage every week, don’t envy me. My massage is not your massage. Consider how a massage would feel if that charley horse you had in your leg last week was all over your body. Massaging it out was very painful, but it had to be done. My body is knot-filled. If I can stand the pain, regular massage can help, at least temporarily.

11. My good days - If you see me smiling and functioning normally, don’t assume I am well or that I have been cured. I suffer from a chronic pain and fatigue illness with no cure. I can have my good days or weeks or even months. In fact, the good days are what keep me going.

12. My uniqueness - Even those who suffer from FMS are not alike. That means I may not have all of the problems mentioned above. I do have pain above and below the waist and on both sides of my body which has lasted for a very long time. I may have migraines or hip pain or shoulder pain or knee pain, but I do not have exactly the same pain as anyone else.
I hope that this helps you understand me, but if you still doubt my pain, your local bookstore, library and the internet have many good books and articles on fibromyalgia.
Author’s note: This letter is based on communications with people throughout the world, males and females, who suffer from fibromyalgia. It does not represent any one of the over 10,000,000 people with FMS, but it can help the healthy person understand how devastating this illness can be. Please do not take these people and their pain lightly. You wouldn’t want to spend even a day in their shoes…or their bodies.

Author unknown……

Read More... WHAT YOU SHOULD KNOW ABOUT FIBROMYALGIA

Disturbed Physician Syndrome

Saturday, April 26, 2008 20:55

Category: Life
DPS - Disturbed Physician Syndrome
"Physicians are psychologically disturbed.
1) They ignore the data.
2) Whatever data there is, they manipulate to say what they want"


 :shocked:
Read More... Disturbed Physician Syndrome

My Fibromyalgia 3/21/07 6:34 AM

Original blog was posted Mar 21, '07 6:34 AM

hi to all, im new at this blog stuff so here i go.

i discovered i have fibromyalgia a few months ago.... i have been running it down for years and years (15), now it finally has a name.

it does explain 99% of the shit that has been bothering me for since i can remember. the funny thing is i went to a pain specialist in israel, the doc works in boston also so he should also know better, (you would think). i gave him my list of complaints pain here, back sticks there, leg kills me there there and there, tremors, buzzing sensation and a few other things that scream fibromyalgia to any one that knows or specializes in pain.

he says handing me back a CDROM..... " i dont know how to read this MRI stuff, but if i can give u a bit of advice... dont give a big list of aches, pains and other symptoms to doctors, it just confuses them". then he proceeded to give me a lumbar injection even though i didnt need it, and i am sure he knew it wouldnt help either.......

so in short, smoke marijuana! yes it will help better than any thing the "docs" can poison you with.

what ever you do just dont start with all those nasty chemicals they will try to get you hooked on with lies and fables. "these pills and patches are great and many people say they work"( just take it for 2 years and well need to switch you over to some thing more expensive).

well to make a long story short, i took em all and the withdrawals (9 days of something eating u from inside your bones) are seriously nasty, chemicals that even the most demented junkie will not have anything to do with.

got Q's ?

ask away, i did my research on the subject and have more knowledge and medical journal abstracts to share.

mazanga...;-}

P.S. marijuana has also helped me stop smoking cigarettes, and that i thought i would never ever be able to do after being seriously addicted to tobacco for almost 30 years.
Read More... My Fibromyalgia 3/21/07 6:34 AM

Letter to Doctors 08/09/06

The following is a letter sent to a specialist 08/09/06, the pain specialist i met with to that date just didn't care. I was at my wits end and had no idea what to do to help myself, or for that matter any idea how to ease the pain I was enduring 24/7.

Letter dated 08/09/06
My name is *** ****** I am (was) 42 years old and i live in Israel. for the last 15 years i have been having back problems and pains, i have come across the mount Sinai neurosurgery page on the web looking for a solution to my problem. Once while i visited NYC i went and saw a neurologist, his diagnosis was that I had degenerative disk disease.

Since then the pain has gotten seriously bad and now there are many things I can not do any more because of it. In addition approx 18 months ago Ii heard a violent crunching cartilage shredding noise in my right hip & thigh, since then I have been told I ripped a muscle and that's all. Me my back and hip area are seriously "out of balance" and so said the physiotherapist I am going to. I have been given pro-tenc machine and Duragesic patches for pain, but the patches makes me physically sick as was the case with Tramadex and all the other pillsI have been given.

I have been to all to many doctors here in Israel trying to isolate what is the problem and how do i fix it, how to get grips on the pain and the other strange things that are happening to my body because of the pressure on my spine.
I have a CT back (1999), MRI x 2 back & hip(2006), EMG x2 (2006) results and blood work. I would appreciate if i could send u the CD's of the CT & MRI(s) to take a look at and tell me what u can do to help me or what else you need. i know this all may sound very strange but i don't really know what else to do to help myself and my back pains are seriously affecting the way i live and raise my children.

CT results
*** ****** is suffering from long term back pain that radiates down to the legs, buzzing sensations in feet. lately feels buzzing down arms and shaking/trembling of the hands and feet. in the past he has been treated (I HAVE NEVER RECEIVED TREATMENT FROM ANY ORTHOPED OR OTHER DOC HERE IN ISRAEL) by orthopedist with CT 1999_ bulging disks c6-7 and l5-s1 on 20/6/05 he was checked by orthopedist at Bellinson hospital MRI was ordered from s1-d12. EMG was also done to arms and legs, EMG 14/7/05 mild lower limbs sensory neuropathy.,. mild rt CTS radiculopathy lt c5-c6,l5-s1. also suffers from vitamin b12 def.



AS OF THIS LETTER I KNEW NOT THE EVIL HORRORS THAT WERE IN STORE FOR ME.
Read More... Letter to Doctors 08/09/06

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