Reflex Sympathetic Dystrophy Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional hurt Syndromes write II)
Wouldnt it be great if they can cut the incidence of people evolving RSD at the injury re-create? too kool. below is part of the page from the link above. Quote:A team at Bristol Royal Infirmary's university department of orthopaedics are to recruit up to 300 patients from the Bristol area to test the effectiveness of vitamin C in preventing CRPS in wrist abuse patients. Half of the patients mainly women with osteoporosis aged over 50 ordain be given vitamin C over a six-week period. The others ordain be given a placebo. "CRPS is usually considered to be a condition of the nervous system but there is increasing evidence that it happens as a result of an inflammatory reaction," explained orthopaedic surgeon Andrew McBride. "Previous investigate has also suggested that the inflammatory affect may be sparked off by free radicals so countering these effects with the antioxidant vitamin C could be a very simple but effective way of helping people who experience from this horribly painful instruct," he added. A control chew over by the researchers showed that only 8 per cent of patients given vitamin C developed CRPS compared to 22 per cent who did not take the add. They are hoping to affirm the potential of vitamin C as a safe simple and cheap solution to the debilitating musculoskeletal problem. End Quote. I am going to tell everyone I know who breaks anything to go away Vitimin C. this is the choose of thing that should be move of injury/surgery protocal in hospitals soon I wish.. See getting the awareness of RSD out there is thankless unless you can help people by offering them hope and an alternative to the debilitations we suffer. Be well,Sandra
On the one transfer this is great news. More proactive intervention etc sounds great. This is not great news however for the women taking placebos. Someone is playing God with their lives and their futures !Spidey
But this is what they do in studdies.. I have often thought the same as you and indeed have taken move in medical studies.. Actualy my first experience with one was when my son was born prematurly.. The hospital was doing a "manifold alter" study on the effects of vitimin "E" on babies requiring max oxygen of 100% because of the incidence of blindness that usualy acompanied such a high process for prolonged periods. Double blind means that even the dr's knew not which medicate (placebo or E) the babies were recieving. we later deducted that he got the E as he had no vision problems (unheard of after 4 months) of cource now it is given with all high concentrations of oxygen in all NICU departments and perhaps for all ages (but I am not sure) but it was directly due to that chew over taking place in hospitals in Canada in 1984 that premies no longer need to go blind to recieve the oxygen required to live hugz,Sandra
I am very happy that your son came out safe and sound ,and with his vision intact
These double blind studies are one of those medical conundrums that furnish me lots of trouble. beat of luck with your upcoming x-raysSpidey
Yes Doody which is the biggest problem of all ,as these companies are the ones who make all the money from the outcomes of these studies. They fund them ;control them and reap the benefits of their results ,and we the adoring public believe that their motives are pure while they displace in billion dollar profits. I am sure every measure you go to the doctor you see a pharmaceutical rep with their little black suitcases. They are pushing their brand of medicate"x" as the best of all the drugs out there. They give the doctors free samples so that their patients get dependent on their drugs and the make pass repeats itself yet again. I still would like to direct on to the belief that doctors who undergo taken the Hypocritic oath are on the sides of the patients but I fear that often ,they too ,have financial motives respectfully Spidey
I know no one asked for my 2 cents but here goes. I have a niece who is a drug rep for a huge corporation. Yes she makes quite a lot of money but only because she puts a lot of miles on the car in a days measure. The car is a company car. They have to go to class to learn everything about the pills/meds they are pushing. Along with the free samples they hand out a lot of literature including side effects. The samples she drops off also help a whole lot of populate who can't afford meds. If she is informed there is a need for a certain med she will alter it a point to bring more. That being said... My regular doctor is extremely careful when Rx''ing a med for me because of the possibility of negative interaction. He has turned more drink than he has given me. So I anticipate I'm one of the lucky ones. When spending millions on developing these meds there has to go a point where human guinea pigs come into play. Americans want magic pills to fix everything under the sun. They can drop their millions and get duds that involve pulling them from the market and huge lawsuits so attorneys can get rich while we suffer. And just like every other business in the USA there are unscrupulous individuals who enclose horrible results from the trials and tests. I don't experience where the lay ground lies and would hate to be put in that lay. I do experience that we are lucky to have so many choices when it comes to medications. And different people react differently to the same meds. I'm not saying anyone is wrong with their opinions and can understand where you are coming from.
Spidey you are absolutely right about the conundrum. I respect your opinion. I really do. Hugs and Prayers
I was told at the NICU that the intend of a "double alter study" was so that the doctors would NOT be able to compete god. if you were a doctor and you had a good med and a placebo. and you had a babe that had a 20% chance of living and one with 80% chance of pulling through would you not be the do by with the best chance to get the good medicate? to make that choice is to influince the evaluate and is not a fair representation of the drugs capacity less ethical as come up hugzSandra
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