Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 I was asked by a congressional staffer the following: "Can you find out if those patients are part of a research study? If so, it may be possible to get you enrolled; especially if it is NIH funded research. Let me know. j" I couldn't find any evidence if NIH in Naltrexone research for use in MS. do any of you have any additional information / in site? Dan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 > > I was asked by a congressional staffer the following: > > " Can you find out if those patients are part of a research study? If so, it may be possible to get you enrolled; especially if it is NIH funded research. Let me know. j " > > I couldn't find any evidence if NIH in Naltrexone research for use in MS. do any of you have any additional information / in site? > Dan ============ There are no clinical trials going on for LDN and MS. There will soon be a clinical trial in PA for Crohn's and LDN. I doubt that MS will get a clinical trial with LDN. There are the big pharmaceutical companies that make Avonex, Betaseron, Copaxone and Rebif that would be jeapordized millions or billions of dollars if a clinical trial for LDN took place. These injectible drugs cost $1200 per month and LDN costs from $11 for 3mg capsules to around $22 for the 4.5mg capsules. These prices would come from Skip's pharmacy in Florida. Skip fills many LDN scripts and can offer LDN at a very cheap price. The big pharmaceutical companies put a halt to Elaine DeLack's Procarin from getting it's clinical trial. The big dogs scared off the pharmaceutical company that had promised Elaine a clinical trial for her Procarin. This shows me that we MS'ers are on our own. I do not trust the MS Society one bit anymore and have quit donating to them. I donate to the MSAA(Multiple Sclerosis Association Of America) who provide wheelchairs, scooters, canes, walkers, ramps, cool suits and many other things that MS'ers need. All the MSAA requires is a script from your neuro stating what assistive device the patient is in need of. Quote Link to comment Share on other sites More sharing options...
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