yellowgenius

Heat and MS

Posted on 06/22/09, 10:50 am

I keep reading and hearing that a lot of peoples MS is affected by the heat—I have not had this be the case for me, is that normal? I have had this thing for almost 14 years now and the lack-of heat thing is making me think I may have been misdiagnosed? Could this be the case or am I one of the ones that heat does not matter?

• Reply #11 10/12/09  12:04pm
  
  yellowgenius
  Been on LDN only since May 5th of this year (2009). Tested for MS with MRI, EEG, Spinal Tap, etc......All test showed nothing but the symptoms (exacerbations) I was having made the Docs (multiple)—diagnose as Probable MS (the year was 1995). I was not happy with them pushing the CRAB drugs so I quit going to the Docs for MS and just dealt with it myself (trying to live a healthy lifestyle). Now, in February of this year (2009) I finally decided to meet with new doctors and go through my entire medical history with them and start LDN as a disease-progress preventative. In talks a research my Doc and I are really starting to look into Lyme and other possible explanations.
• Reply #12 10/16/09  3:46pm
  
  LarryLDN
  I also refused the CRABs and figured I'd go to an allergist to find out what could trigger problems. I got a full list in 2003, a month before going on LDN, which pretty much matched my 1972 list.
  
  I went back 9/07 for a re-run of those tests and all my food allergies were gone! http://www.larrygc.com/mystory the results of those tests are in my story link
• Reply #13 10/16/09  3:48pm
  
  LarryLDN
  I've been in the high heat & humidity of Florida since last Wednesday, I seem to be walking a lot better than I do in the colder areas. We'll see if it continues to improve in that dept

LDN .. Low Dose Naltrexone 3.0 MG or 4.5 MG ...... Helps ALL AutoImmune diseases not just MS