Guest guest Posted May 12, 2004 Report Share Posted May 12, 2004 ELAINE - I JUST STARTED LDN AND I TAKE COPAXONE. I'VE NEVER HAD AND PROBLEMS WITH COPAXONE OR SIDE EFFECTS. DR. B TOLD ME TO STAY ON IT AT LEAST 3 MONTHS BEFORE MAKING A DECISION TO STOP OR NOT. IF YOU CHOSE COPAXONE WOULD BE THE BEST CHOICE. KIM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2004 Report Share Posted May 12, 2004 Hi kathy, Thanks for the message, I already know I want to try the LDN, I don't want to be sticking needles in myself for the rest of my life. I will NEVER take any of the interferons, I'll consider copaxone ,but only after giving LDN a try first. After that I hope there is no need for it. My neuro wanted to send me to a MS research hosp. for a 2nd opinion (after refusing to look at my LDN info) he told me to ask them about it, then we would talk again, He got me an appointment in July, and after reading all the messages on the board this week about the MS Societys I decided to call this MS " expert " and see if he would at least be willing to consider LDN but they gave me a flat out NO. They would only prescibe the abcr's so I cancelled on the spot. Why waste my time. So I called a neuro locally that my GP said was off the beaten path, (that's why he DIDN " T send me to him) And over the phone he seemed willing to try anything that I thought would work as long he deems it not harmful. So I now have an app. for next week (thank goodness not 2mths from now) I'll be packing all my info and I won't leave till he throws me out or I get the ldn. wish me luck Elaine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2004 Report Share Posted May 12, 2004 Elaine - Good luck with the doctor. I felt exactly the same as you on the injectables - MIGHT try copaxane, but only after trying LDN. I have been on LDN for 26 days, and while it has been a little weird, I am SO happy that I made this decision. Best Wishes - Cinders Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2004 Report Share Posted May 12, 2004 GO GIRL!!!! -------Original Message------- From: low dose naltrexone Date: Wednesday, May 12, 2004 09:53:13 low dose naltrexone Subject: [low dose naltrexone] to flashykathy Hi kathy,Thanks for the message, I already know I want to try the LDN, I don't want to be sticking needles in myself for the rest of my life. I will NEVER take any of the interferons, I'll consider copaxone ,but only after giving LDN a try first. After that I hope there is no need for it. My neuro wanted to send me to a MS research hosp. for a 2nd opinion (after refusing to look at my LDN info) he told me to ask them about it, then we would talk again, He got me an appointment in July, and after reading all the messages on the board this week about the MS Societys I decided to call this MS "expert" and see if he would at least be willing to consider LDN but they gave me a flat out NO. They would only prescibe the abcr's so I cancelled on the spot. Why waste my time. So I called a neuro locally that my GP said was off the beaten path, (that's why he DIDN"T send me to him) And over the phone he seemed willing to try anything that I thought would work as long he deems it not harmful. So I now have an app. for next week(thank goodness not 2mths from now) I'll be packing all my info and I won't leave till he throws me out or I get the ldn. wish me luckElaine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2004 Report Share Posted May 12, 2004 Good Luck Kathy! What town are you in if I may ask. -------Original Message------- From: low dose naltrexone Date: Wednesday, May 12, 2004 08:54:21 low dose naltrexone Subject: [low dose naltrexone] to flashykathy Hi kathy, Thanks for the message, I already know I want to try the LDN, I don't want to be sticking needles in myself for the rest of my life. I will NEVER take any of the interferons, I'll consider copaxone ,but only after giving LDN a try first. After that I hope there is no need for it. My neuro wanted to send me to a MS research hosp. for a 2nd opinion (after refusing to look at my LDN info) he told me to ask them about it, then we would talk again, He got me an appointment in July, and after reading all the messages on the board this week about the MS Societys I decided to call this MS "expert" and see if he would at least be willing to consider LDN but they gave me a flat out NO. They would only prescibe the abcr's so I cancelled on the spot. Why waste my time. So I called a neuro locally that my GP said was off the beaten path, (that's why he DIDN"T send me to him) And over the phone he seemed willing to try anything that I thought would work as long he deems it not harmful. So I now have an app. for next week (thank goodness not 2mths from now) I'll be packing all my info and I won't leave till he throws me out or I get the ldn. wish me luck Elaine Quote Link to comment Share on other sites More sharing options...
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