Guest guest Posted June 3, 2003 Report Share Posted June 3, 2003 I had my telephone interview with Dr Sullivan this afternoon. He wanted me to try to get a blood test for Cahdida antibody tire Probably from Immuno Sciences. He also would like to see the results of the heavy metal test I had taken last week. Interesting, my nuro never even considered these possibilities. He based the Cahdida antibody tire test on the fact that I have had some problems with gas. ----- Original Message ----- From: CK Connie King (1452) low dose naltrexone Sent: Tuesday, June 03, 2003 7:02 AM Subject: RE: [low dose naltrexone] 31 Days I'm trying to convince someone I know to consider LDN. She's in a wheelchair and has been for quite some time. She's in her 60's. She's constantly fatigued and suffers with spasms, etc. Is anyone taking LDN that is or was in a wheelchair? What have been your experiences with LDN? Did you stop your other medications? -----Original Message-----From: blueswede06 [mailto:blueswede06@...]Sent: Monday, June 02, 2003 12:59 AMlow dose naltrexone Subject: [low dose naltrexone] 31 DaysHello friends and fellow MSers, Tonight I just took my 31 st dose of LDN. Hard to believe it has been a full month. What a difference it has made in my life. Pain is greatly decreased, spasms are almost non existant, fatigue is very rare, and overall I feel the best I have felt in 5-6 years. Have noticed an improvement in my vision, and short term memory. Thank God, I again have the drive to enjoy life, and all of its downs. This week I lost the person who comes in during the day to stay with my elderly mother. Moved her in with me two years ago, after dad passed away, as she cannot be alone. Pre-LDN, I probably would have become very depressed and withdrawn. With LDN, I'm not stressing, just getting things taken care of. To anyone unsure of this drug, all I can say is try it. Will it stop MS? I don't know yet, but it has greatly improved the quality of my life. I can't afford to retire or disability out, so I must continue working and taking care of family. Without the LDN, I would probably fail miserably at this. I am not taking ABCR drugs, never have, and most likely never will. Everything I have seen and read, they look like some really high priced snake oil to me. The drug companies are getting rich on them, but the users continue to suffer. I am writing this in the hopes that my story may help some other unfortunate soul, in dealing with their MS. If I can help at least one other person, the time spent is well worth it.Good luck to all, I will continue to update you on my progress. I see the neurosurgeon June 9th, to review the latest MRI of the thorasic spine(this is where my large lesion resides). Guy Quote Link to comment Share on other sites More sharing options...
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