Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 Hallo ! LDN is not a medication against symptoms but it stopps progression and so in some cases symptoms may improve.I take LDN for about 1 year,fatigue,pain,bladder have improved.I you get worse fast you are chronic rogressiv now.No interferon can help you,therefore your only chance is to try LDN,you can get a perscripton from your doctor and order it from a pharmacy. Good Luck Dr.Fuhrmann Manfred http://naltrexoneforum.thit.de [low dose naltrexone] thinging about taking LDN > Hello. I'm brand new here. I'm 49 and have had MS for > 16 years and now getting worse fast. Been on Copaxone > for 5 years and don't see any improvement. > Can I get this LDN from my Doctor? Exactly what > symptoms of MS does it help? What side effects? Would > love to hear some good success stories. Thanks. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 http://www.larrygc.com/mystory is my story. [low dose naltrexone] thinging about taking LDN Hello. I'm brand new here. I'm 49 and have had MS for16 years and now getting worse fast. Been on Copaxonefor 5 years and don't see any improvement.Can I get this LDN from my Doctor? Exactly whatsymptoms of MS does it help? What side effects? Wouldlove to hear some good success stories. Thanks. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2005 Report Share Posted July 31, 2005 > Hello. I'm brand new here. I'm 49 and have had MS for > 16 years and now getting worse fast. Been on Copaxone > for 5 years and don't see any improvement. > Can I get this LDN from my Doctor? Exactly what > symptoms of MS does it help? What side effects? Would > love to hear some good success stories. Thanks. > ======= , LDN's main purpose is to halt disease progression, not improve symptoms. If one does happen to get symptom improvement while on LDN then that is an added plus. Go to the LDN website and read it thoroughly...including the Further Q & A page...there's lots of info there on that page. Read the section What Others Are Saying About LDN. That section is an accumulation of posts made here on this forum. LDN website http://www.low dose naltrexone.org Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2005 Report Share Posted July 31, 2005 I have been diagnosed with MS for over 2 years I think stress brought it on (stress does mess up your body) I am on Neiper protocol calcium EAP, I take Sphingolin, and I just started LDN. Friends of mine who are taking the Orthodox way are not doing well, they were good in there 30's and now in there 50's are doing bad, is everyone like this I know MS is different for everyone can you live a long quality life? What about certain herbs? Thank you lkilcollin@aol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2005 Report Share Posted July 31, 2005 DO YOU MEAN YOUR DOING THE IV PUSH 3 TIMES A WEEK WITH CALCIUM EAP? I AM TAKING LDN AND DOING IV CALCIUM EAP BUT I ONLY DO THE SHOTS ONCE A MONTH WHEN I NEED A BOAST. I DID THEM 3 TIMES A WEEK FOR FOUR YEARS AND THEN JUST TAPERED OFF SLOWLY WHILE REMAINING ON THE ORAL IT WORKED SO WELL. YOU SHOULD DO REALLY WELL AS THEY BOTH WORK TOGETHER. TURMERIC OR CURCUMIN IS PROBABLY THE HERB THAT HAS SHOWN THE MOST PROMISE FOR MS. I WOULDN'T GO ADDING ALOT OF HERBS WITH WHAT YOU ARE TAKING BECAUSE DR. NEIPER SAID TIO BE CAREFUL OF THE INTERACTION. HOWEVER, RESEARCHING CERTAIN HERBS AND TRYING THEM WITH CAUTION SHOULD DO YOU NO HARM . cURCUMIN IS SOMETHING I USE NOW AND I LIKE IT. THE SPHINGOLIN IS ALSO AN EXCELLENT PRODUCT YOU ARE USING. I WOULD ADD SOME GOOD ENZYMES AND KRILL OIL TO YOUR REGIMEN IF YOU HAVEN'T ALREADY. BLESSINGS, KATHY Re: [low dose naltrexone] thinging about taking LDN I have been diagnosed with MS for over 2 years I think stress brought it on (stress does mess up your body) I am on Neiper protocol calcium EAP, I take Sphingolin, and I just started LDN. Friends of mine who are taking the Orthodox way are not doing well, they were good in there 30's and now in there 50's are doing bad, is everyone like this I know MS is different for everyone can you live a long quality life? What about certain herbs? Thank you lkilcollin@aol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2005 Report Share Posted August 1, 2005 My wife, who is RR, experienced drastic reduction in headache frequency and intensity. She had had a debilitating headache non stop for 8 months. Also greatly improved bladder and bowel function, balance, cognitive abilities, especially memory. Her energy and stamina are much better. Sleep is better quality. The biggest change has been in skin sensation. The bottoms of her feet were dead numb since the first exacerbation in 1996. After 13 months of LDN, she now can feel her feet and can even feel texture almost as well as pre MS. She curses me (jokingly) every time she walks on gravel without shoes. I pushed her for and her neurologist for 3 years to try LDN. She used to walk bare foot on gravel and feel nothing, now she has to limp across it due to the pain, which is fantastic. Also, the last 2 consecutive MRIs have shown reduction in size of all lesions. fm2 wrote: > Hallo ! > LDN is not a medication against symptoms but it stopps progression and > so in > some cases symptoms may improve.I take LDN for about 1 > year,fatigue,pain,bladder have improved.I you get worse fast you are > chronic > rogressiv now.No interferon can help you,therefore your only chance is to > try > LDN,you can get a perscripton from your doctor and order it from a > pharmacy. > Good Luck > Dr.Fuhrmann Manfred > http://naltrexoneforum.thit.de > > [low dose naltrexone] thinging about taking LDN > > > > Hello. I'm brand new here. I'm 49 and have had MS for > > 16 years and now getting worse fast. Been on Copaxone > > for 5 years and don't see any improvement. > > Can I get this LDN from my Doctor? Exactly what > > symptoms of MS does it help? What side effects? Would > > love to hear some good success stories. Thanks. > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2005 Report Share Posted August 1, 2005 Hi Wes! I know how she feels...two and a half years prior to being dx'd with rrms, I had severe migraines...then 22 months on one of the CRAB meds, still had the migraines...Dec11th, 2003, took my first dose of ldn, next day... after a half hour of trying to figure out what was different, I finally came to the conclusion...NO MORE HEADACHE!!! That was just one of the many things that 'seemed' to be either gone, or lessened to such a small degree that most things are now easily tolerated. Best of luck to your wife and keep us posted on how she's doing. Have a Great Day everyone! Jim(rrms) now...back to my cave :-) Re: [low dose naltrexone] thinging about taking LDN My wife, who is RR, experienced drastic reduction in headache frequency and intensity. She had had a debilitating headache non stop for 8 months. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2005 Report Share Posted August 1, 2005 Wesley- Thanks for posting this. It is great to hear. I am new to LDN, and hearing your wife's story gives me such hope for myself and my loved ones who are also on LDN. Take care, AmyWesley wrote: My wife, who is RR, experienced drastic reduction in headache frequency and intensity. She had had a debilitating headache non stop for 8 months. Also greatly improved bladder and bowel function, balance, cognitive abilities, especially memory. Her energy and stamina are much better. Sleep is better quality. The biggest change has been in skin sensation. The bottoms of her feet were dead numb since the first exacerbation in 1996. After 13 months of LDN, she now can feel her feet and can even feel texture almost as well as pre MS. She curses me (jokingly) every time she walks on gravel without shoes. I pushed her for and her neurologist for 3 years to try LDN. She used to walk bare foot on gravel and feel nothing, now she has to limp across it due to the pain, which is fantastic. Also, the last 2 consecutive MRIs have shown reduction in size of all lesions.__________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2005 Report Share Posted August 1, 2005 that is wonderful news. kathy [low dose naltrexone] thinging about taking LDN>>> > Hello. I'm brand new here. I'm 49 and have had MS for> > 16 years and now getting worse fast. Been on Copaxone> > for 5 years and don't see any improvement.> > Can I get this LDN from my Doctor? Exactly what> > symptoms of MS does it help? What side effects? Would> > love to hear some good success stories. Thanks.> > > >> >> >> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2005 Report Share Posted August 1, 2005 > My wife, who is RR, experienced drastic reduction in headache frequency > and intensity. She had had a debilitating headache non stop for 8 > months. Also greatly improved bladder and bowel function, balance, > cognitive abilities, especially memory. Her energy and stamina are much > better. Sleep is better quality. The biggest change has been in skin > sensation. The bottoms of her feet were dead numb since the first > exacerbation in 1996. After 13 months of LDN, she now can feel her feet > and can even feel texture almost as well as pre MS. She curses me > (jokingly) every time she walks on gravel without shoes. I pushed her > for and her neurologist for 3 years to try LDN. She used to walk bare > foot on gravel and feel nothing, now she has to limp across it due to > the pain, which is fantastic. Also, the last 2 consecutive MRIs have > shown reduction in size of all lesions. > ========= I also got reduction of migraines on LDN. I was having migraines weekly for about 2 years straight. Now I only have a migraine the week before my menses cycle but I can keep that migraine away if I remember to take Ibuprofen the entire week before my menses, my gyno told me to try the Ibuprofen. So far the Ibuprofen the week before menses is the ONLY thing that will keep that migraine away. Once the migraine has started absolutely no medication touches it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2005 Report Share Posted August 2, 2005 > > > My wife, who is RR, experienced drastic reduction in headache frequency > > > and intensity. She had had a debilitating headache non stop for 8 > > > months. Also greatly improved bladder and bowel function, balance, > > > cognitive abilities, especially memory. Her energy and stamina are > > much > > > better. Sleep is better quality. The biggest change has been in skin > > > sensation. The bottoms of her feet were dead numb since the first > > > exacerbation in 1996. After 13 months of LDN, she now can feel her > > feet > > > and can even feel texture almost as well as pre MS. She curses me > > > (jokingly) every time she walks on gravel without shoes. I pushed her > > > for and her neurologist for 3 years to try LDN. She used to walk bare > > > foot on gravel and feel nothing, now she has to limp across it due to > > > the pain, which is fantastic. Also, the last 2 consecutive MRIs have > > > shown reduction in size of all lesions. > > > > > ========= > > > > I also got reduction of migraines on LDN. I was having migraines > > weekly for about 2 years straight. Now I only have a migraine the > > week before my menses cycle but I can keep that migraine away if I > > remember to take Ibuprofen the entire week before my menses, my gyno > > told me to try the Ibuprofen. So far the Ibuprofen the week before > > menses is the ONLY thing that will keep that migraine away. Once the > > migraine has started absolutely no medication touches it. > > > > > > has the same problem pre and during. For those particular > headaches, she's found Excedrin, or generic, works better than anything > else. > ========== I've tried Excedrine, Excedrine Migraine and Excedrine Tension Headache and Midol and nothing touches the migraine once it starts. And it never fails, the menstrual migraine is always on the left side of my head, never on the right side. That menstrual migraine pounds with my every heartbeat. I hate that part of being a woman. It's cruel and unusual punishment to have to have a menses cycle. Quote Link to comment Share on other sites More sharing options...
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