Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 2yrs 8 mths. It's hard for me to tell as I was so progressed to start with. This past infection kicked my rear (2 wks ago). Heat has been rough, even though I'm not out in it. At this moment, I feel like hammered heck! MarcieBren <b63powell@...> wrote: Who all looking in has been on LDN no less than 2 1/2 years? For those who are at or over the 2 1/2 year mark, how long have you been on LDN? Has LDN halted or slowed your disease progression and what illness or illnesses do you take LDN for? I have been on LDN 3 years. LDN has halted my MS and Lupus progression. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 I forgot..PPMS. MarcieMarcie <marcie_martin@...> wrote: 2yrs 8 mths. It's hard for me to tell as I was so progressed to start with. This past infection kicked my rear (2 wks ago). Heat has been rough, even though I'm not out in it. At this moment, I feel like hammered heck! MarcieBren <b63powell@...> wrote: Who all looking in has been on LDN no less than 2 1/2 years? For those who are at or over the 2 1/2 year mark, how long have you been on LDN? Has LDN halted or slowed your disease progression and what illness or illnesses do you take LDN for? I have been on LDN 3 years. LDN has halted my MS and Lupus progression. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 LDN for MS..2 years and 7 months...stopped/halted the progression, and an 'almost' complete turnaround of symptoms. Still have major fatigue & weakness, and some 'bowel' issues... (blush) ... on the bright side...at least I'm not 'stopped' up. :-) All other symptoms are very very mild and are easily ignored. I know I know...bad Caveman...I'll trudge back into my Cave....grumblegrumble shuffle shuffle....(stumble)...ouch....sigh....yawn....zzzzzzz Cap'n Caveman [low dose naltrexone] How many have been on LDN 2 1/2 yrs or more? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 Hi All, It’s been 2 years 7 months on LDN for my MS. The first few months I notice a lot of symptom relief as I was going downhill before quickly. Bren <b63powell@...> wrote: Who all looking in has been on LDN no less than 2 1/2 years? For those who are at or over the 2 1/2 year mark, how long have you been on LDN? Has LDN halted or slowed your disease progression and what illness or illnesses do you take LDN for? I have been on LDN 3 years. LDN has halted my MS and Lupus progression. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 > > 2yrs 8 mths. It's hard for me to tell as I was so progressed to start with. This past infection kicked my rear (2 wks ago). Heat has been rough, even though I'm not out in it. At this moment, I feel like hammered heck! > > Marcie > >============= Marcie, It may take your immune system some time to bounce back from having such a severe infection. You also had antibiotics and that is not good. Make sure you take a good quality probiotic up to 2 to 4 per day. This summer's heat has been awful too. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 I have been on LDN since 11/03 . I feel it has halted the progression of my ms. It did take about 3-6 months before I could really tell it was strengthening my system. I felt so much stronger emotionally. Bad news would not bring about symptoms. I felt fortified. Anyway, I am very thankful and wish this for everyone. Don't wait to try this treatment. It is much harder to reverse nerve damage and I really feel time is so important with ms. However, it is never too late to start. That is why some people have these dramatic improvements. Their myelin was not destroyed. No test can tell how much myelin you have on your sheath that I know of. Sometimes a nerve is damaged just enough that it causes loss of sight but it can be rebuilt because there are the oligodendrocytes which are constantly working to rebuild in a regulated immune system. My point is not even the top neuro knows what improvements are possible for each individual. A person can have an MRI totally filled with lesions and be asymptomatic,. Another can have a clean MRI and not be walking. Never give up. The human body is capable of tremendous healing. Best, Kathy [low dose naltrexone] How many have been on LDN 2 1/2 yrs or more? Who all looking in has been on LDN no less than 2 1/2 years? For those who are at or over the 2 1/2 year mark, how long have you been on LDN? Has LDN halted or slowed your disease progression and what illness or illnesses do you take LDN for? I have been on LDN 3 years. LDN has halted my MS and Lupus progression. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 Marcie, I've been taking LDN for 2 year and seven months. I've been following Dr. Lawrence's supplement recommendations since last November and have been doing better, yet this heat and humidity have been causing me to regress. Since taking GABA, my leg spasms had practically disappeared, but in this weather... I checked my notes from Bob Lawrence. (Aletha sends them out with the welcome package, for anyone new). He normally recommends taking anthocyanidins daily: 250-500 mg. But in times of severe stress you can take up to 1000. I currently take 500, but until the weather breaks I'm going to take 1000. The cheapest flavonoid is grapeseed extract. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 > > Marcie, I've been taking LDN for 2 year and seven months. > > I've been following Dr. Lawrence's supplement recommendations since > last November and have been doing better. Since taking GABA, my leg spasms had > practically disappeared, but in this weather... > > I checked my notes from Bob Lawrence. He normally recommends taking > anthocyanidins daily: 250-500 mg. But in times of severe stress you > can take up to 1000. I currently take 500, but until the weather > breaks I'm going to take 1000. The cheapest flavonoid is grapeseed > extract. > > > > ======= , It's great to see you and Marcie posting again. I have felt lonely in here since so many oldtimers departed. Marcie has so much difficulty with spasticity that any suggestion would be of help. Do you know how long Dr. Lawrence has been taking LDN and how he is currenly doing? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 Welcome back, ! > > >He normally recommends taking > anthocyanidins daily: 250-500 mg. But in times of severe stress you > can take up to 1000. I currently take 500, but until the weather > breaks I'm going to take 1000.< > > Hi , what exactly does this do for you? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 >From: " Kathy Lintzenich " <mykittypaws@...> >Reply-low dose naltrexone ><low dose naltrexone > >Subject: Re: [low dose naltrexone] How many have been on LDN 2 1/2 yrs or >more? >Date: Sun, 23 Jul 2006 08:02:27 -0700 > >I have been on LDN since 11/03 . I feel it has halted the progression of my >ms. It did take about 3-6 months before I could really tell it was >strengthening my system. I felt so much stronger emotionally. Bad news >would not bring about symptoms. I felt fortified. Anyway, I am very >thankful and wish this for everyone. Don't wait to try this treatment. It >is much harder to reverse nerve damage and I really feel time is so >important with ms. However, it is never too late to start. That is why >some people have these dramatic improvements. Their myelin was not >destroyed. No test can tell how much myelin you have on your sheath that I >know of. Sometimes a nerve is damaged just enough that it causes loss of >sight but it can be rebuilt because there are the oligodendrocytes which >are constantly working to rebuild in a regulated immune system. My point is >not even the top neuro knows what improvements are possible for each >individual. A person can have an MRI totally filled with lesions and be >asymptomatic,. Another can have a clean MRI and not be walking. Never give >up. The human body is capable of tremendous healing. Best, Kathy > [low dose naltrexone] How many have been on LDN 2 1/2 yrs or >more? > > > > Who all looking in has been on LDN no less than 2 1/2 years? For those >who are at or over the 2 1/2 year mark, how long have you been on LDN? Has >LDN halted or slowed your disease progression and what illness or illnesses >do you take LDN for? > > I have been on LDN 3 years. LDN has halted my MS and Lupus progression. > > > > > > _________________________________________________________________ Don’t just search. Find. Check out the new MSN Search! http://search.msn.click-url.com/go/onm00200636ave/direct/01/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 >From: " Mariela Contreras " <marielacm16@...> >Reply-low dose naltrexone >low dose naltrexone >Subject: Re: [low dose naltrexone] How many have been on LDN 2 1/2 yrs or >more? >Date: Sun, 23 Jul 2006 13:01:28 -0400 > > > > > >From: " Kathy Lintzenich " <mykittypaws@...> > >Reply-low dose naltrexone > ><low dose naltrexone > > >Subject: Re: [low dose naltrexone] How many have been on LDN 2 1/2 yrs or > >more? > >Date: Sun, 23 Jul 2006 08:02:27 -0700 > > > >I have been on LDN since 11/03 . I feel it has halted the progression of >my > >ms. It did take about 3-6 months before I could really tell it was > >strengthening my system. I felt so much stronger emotionally. Bad news > >would not bring about symptoms. I felt fortified. Anyway, I am very > >thankful and wish this for everyone. Don't wait to try this treatment. It > >is much harder to reverse nerve damage and I really feel time is so > >important with ms. However, it is never too late to start. That is why > >some people have these dramatic improvements. Their myelin was not > >destroyed. No test can tell how much myelin you have on your sheath that >I > >know of. Sometimes a nerve is damaged just enough that it causes loss of > >sight but it can be rebuilt because there are the oligodendrocytes which > >are constantly working to rebuild in a regulated immune system. My point >is > >not even the top neuro knows what improvements are possible for each > >individual. A person can have an MRI totally filled with lesions and be > >asymptomatic,. Another can have a clean MRI and not be walking. Never >give > >up. The human body is capable of tremendous healing. Best, Kathy > > [low dose naltrexone] How many have been on LDN 2 1/2 yrs or > >more? > > > > > > > > Who all looking in has been on LDN no less than 2 1/2 years? For those > >who are at or over the 2 1/2 year mark, how long have you been on LDN? >Has > >LDN halted or slowed your disease progression and what illness or >illnesses > >do you take LDN for? > > > > I have been on LDN 3 years. LDN has halted my MS and Lupus >progression. > > > > > > > > > > > > > >_________________________________________________________________ >Don’t just search. Find. Check out the new MSN Search! >http://search.msn.click-url.com/go/onm00200636ave/direct/01/ > > > > > > Quote Link to comment Share on other sites More sharing options...
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