Using LDN for MS

[Guest guest]

I want to give you a little warning. I had a very similar initial reaction when

first starting LDN with very similar symptoms. I began to feel much better over

the course of about 3 months. In the following 3 months after that, I began to

get much worse.

If this happens to you, it could be indicative of a systemic bacterial infection

such as Borellia (Lyme Disease) or any number of its coinfections (Babesia,

Bartonella, Erillichia, Mycoplasma, etc.).

If you find yourself getting a lot worse after feeling better on LDN, you much

get properly tested for Lyme disease. Only IGENEX labs in California properly

tests for Lyme. If your doctor tries to use Quest or LabCorps to process your

Lyme ELISA and Western Blots, find a different doctor. Only IGENEX tests the

correct bands.

I'm very pleased to hear of your progress with LDN, but be on the lookout.

Wishing you well.

- KenC.

>

>

> Hi Everyone,

>

> Thought I should write and let you know what has happened to me since I

started using LDN. I was fortunate in finding a doctor who was willing to

subscribe LDN for my MS.

>

> I was diagnosed with MS 6 years ago. I thought I had a pretty good control of

MS, didn't seem to have any serious effects (to my mind). I have subsequently

found out that a number of problems that I have had is a result of my MS. I

have had cramping and pains in my legs and feet for a number of years.

Developed numbness in my fingers. Finally went to my doctor and confirmed that

these were symptoms of MS. Also found out that the memory problems that I have

been having over the years is a result of MS. Also the fog that I felt was in

was also a symptom.

>

> Anyways, just to let you know, I have only taken 3mg of LDN for 4 days now and

I can confirm that the pain in my feet and legs are gone. The numbness in my

fingers is gone, as well as the fog I was experiencing is also gone.

>

> When I started taking LDN I was skeptical that it would work for me. I

thought that I would be one of the few that it wouldn't help. Imagine my

surprise when after the very first day, my feet no longer felt cold and had no

pain. And day after day the pain that I have had in my legs is completely gone.

I no longer feel fatigue and tiredness when I get up in the morning. I feel

more alive that I have felt in such a long time. I feel like myself again.

>

> Anyone who is considering taking LDN and is skeptical about taking it, I say

" Give it a chance. It may surprise you. " just like it did me.

>

> Everyone has such inspirational stories that it makes me feel good that I

found this.

>

> I was so impressed that I went to my Local MS Society Chapter to let them know

what I've found out. I gave the web site www.low dose naltrexone.com so that they

can do their own research. My personal opinion is that I think everyone with MS

should know about LDN and how it can change your life. This is an alternative

to CCSVI which is not available to me where I live, while LDN is.

>

> Just thought I should let you know how in just a short short time LDN has

changed me.

>

> Thank you.

>

[Guest guest]

Thank you for the encouragement and support. I will continue to monitor and hope I don't have any issues down the road.

Sorry about getting the address wrong. Yes it should be www.low dose naltrexone.org. Will keep that in mind if I tell anybody else.

Thanx again.

[Guest guest]

My MS was LYME and CO-Infections! I wasn't thinking LYME when I first came here, I was thinking MS.

Sorry, have been out of the loop for a while.

LDN helped me figure it out, and my 4th LYME test (done through IGENEX)

Still wonder if all of these could really be LYME and CO-infections related (sorry to repeat again):

www.canlyme.com, symptomns..........

"Many Lyme patients were firstly diagnosed with other illnesses such as Juvenile Arthritis, Rheumatoid Arthritis, Reactive Arthritis, Infectious Arthritis, Osteoarthritis, Fibromyalgia, Raynaud's Syndrome, Chronic Fatigue Syndrome, Interstitial Cystis, Gastroesophageal Reflux Disease, Fifth Disease, Multiple Sclerosis, scleroderma, lupus, early ALS, early Alzheimers Disease, crohn's disease, ménières syndrome, reynaud's syndrome, sjogren's syndrome, irritable bowel syndrome, colitis, prostatitis, psychiatric disorders (bipolar, depression, etc.), encephalitis, sleep disorders, thyroid disease and various other illnesses. see Other Diseases and Lyme...Relationship "

Good luck to all of you trying LDN! May you get some, if not more, of the same positive results I have!

BRAD, the Angry Engineer (and LYMIE). But I am not a doctor! And I am taking antibiotics again in 2011 with my LDN.

Don't ask me, ask Gabbi www.withatwistoflyme.org How does a teenager, or a child, deal with being told it's all in their head, it's not LYME, when it's not all in their head? Was hard enough as an adult!

From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of cleremond2000Sent: Wednesday, April 13, 2011 2:13 PMlow dose naltrexone Subject: [low dose naltrexone] Re: Using LDN for MSImportance: High

I want to give you a little warning. I had a very similar initial reaction when first starting LDN with very similar symptoms. I began to feel much better over the course of about 3 months. In the following 3 months after that, I began to get much worse.If this happens to you, it could be indicative of a systemic bacterial infection such as Borellia (Lyme Disease) or any number of its coinfections (Babesia, Bartonella, Erillichia, Mycoplasma, etc.).If you find yourself getting a lot worse after feeling better on LDN, you much get properly tested for Lyme disease. Only IGENEX labs in California properly tests for Lyme. If your doctor tries to use Quest or LabCorps to process your Lyme ELISA and Western Blots, find a different doctor. Only IGENEX tests the correct bands.I'm very pleased to hear of your progress with LDN, but be on the lookout.Wishing you well.- KenC.>> > Hi Everyone,> > Thought I should write and let you know what has happened to me since I started using LDN. I was fortunate in finding a doctor who was willing to subscribe LDN for my MS.> > I was diagnosed with MS 6 years ago. I thought I had a pretty good control of MS, didn't seem to have any serious effects (to my mind). I have subsequently found out that a number of problems that I have had is a result of my MS. I have had cramping and pains in my legs and feet for a number of years. Developed numbness in my fingers. Finally went to my doctor and confirmed that these were symptoms of MS. Also found out that the memory problems that I have been having over the years is a result of MS. Also the fog that I felt was in was also a symptom.> > Anyways, just to let you know, I have only taken 3mg of LDN for 4 days now and I can confirm that the pain in my feet and legs are gone. The numbness in my fingers is gone, as well as the fog I was experiencing is also gone.> > When I started taking LDN I was skeptical that it would work for me. I thought that I would be one of the few that it wouldn't help. Imagine my surprise when after the very first day, my feet no longer felt cold and had no pain. And day after day the pain that I have had in my legs is completely gone. I no longer feel fatigue and tiredness when I get up in the morning. I feel more alive that I have felt in such a long time. I feel like myself again.> > Anyone who is considering taking LDN and is skeptical about taking it, I say "Give it a chance. It may surprise you." just like it did me.> > Everyone has such inspirational stories that it makes me feel good that I found this. > > I was so impressed that I went to my Local MS Society Chapter to let them know what I've found out. I gave the web site www.low dose naltrexone.com so that they can do their own research. My personal opinion is that I think everyone with MS should know about LDN and how it can change your life. This is an alternative to CCSVI which is not available to me where I live, while LDN is.> > Just thought I should let you know how in just a short short time LDN has changed me. > > Thank you.>