Re: One year on LDN and Marie

[Guest guest]

To and Marie,

both of you are proof of long term use (longer than me anyhow) and

safety, results and positive outcomes with LDN - Marie, your MRI

result is fantastic, and I hope your neuro accredits it to LDN, same

with all neuro's - they need to support it's use for MS and put their

comments and patient's results on a section/page of the LDN

Organisations website. Then, at the same time, all other conditions

will follow, with the success stories, in making it easier to access

from the medicos. This is more concrete support than anectodal's

alone dont you think?

BOth of your results are very encouraging. Good on you!! and

thankyou for your prayers.

Friday

- In low dose naltrexone , " Marie Deady " <Mardea@b...>

wrote:

> Hi

> Congradulation on your victory. I just realized that yesterday

(June 3rd) was my one year anniversary with LDN too. I am also doing

good. My spasms are much better and have been able to cut my spasms

medication in half. But I had an MRI and they saw no progression in

my disease. That was the first time that they saw no progression. I

am so happy about that. Please let us know how your MRI turns out.

Good Luck

> Marie

> ----- Original Message -----

> From: Doherty

> LDN chat ; MS watch chat ; Spotlight LDN

> Sent: Thursday, June 03, 2004 9:16 PM

> Subject: [low dose naltrexone] One year on LDN

> Hello fellow MSers!

>

Just wanted to let you all know that I've been on LDN for exactly one

year this Memorial Day weekend. This time last year I could barely

walk without pain and stiffness. At one point I couldn't even wear

shoes or socks Now there are days when I forget I even have MS. (I

also take collodial silver, calcium aep and digestive enzymes). So

for those of you just starting LDN please hang in there. It may take

a while but I honestly believe in it. I am not 100% healed but am

doing so much better. The only problem I have are stilll some

numbness in my legs and feet that are still s-l-o-w-l-y subsiding. I

plan on getting new MRIs done this summer and will update you all.

Please stay positive, LDN works very slowly but it does work. I am

praying and thinking of all of you as I read all your messages.

>

> Your friend,

>

[Guest guest]

Hi Friday,

You know the strange thing about doing so good, I don't think that my neuro even thinks that the report from the MRI has anything to do with the LDN. He wasn't for the LDN to start, so I had to have Dr Bihari prescribe it. Now that I am doing so good, I think that he thinks that I will eventually get worst. I will prove him wrong. My GP is impressed though. She is very excited to hear my progress when I see her. Wishing you the best.

Marie

----- Original Message -----

From: Friday

low dose naltrexone

Sent: Friday, June 04, 2004 9:12 AM

Subject: [low dose naltrexone] Re: One year on LDN and Marie

To and Marie,both of you are proof of long term use (longer than me anyhow) and safety, results and positive outcomes with LDN - Marie, your MRI result is fantastic, and I hope your neuro accredits it to LDN, same with all neuro's - they need to support it's use for MS and put their comments and patient's results on a section/page of the LDN Organisations website. Then, at the same time, all other conditions will follow, with the success stories, in making it easier to access from the medicos. This is more concrete support than anectodal's alone dont you think?BOth of your results are very encouraging. Good on you!! and thankyou for your prayers.Friday- In low dose naltrexone , "Marie Deady" <Mardea@b...> wrote:> Hi > Congradulation on your victory. I just realized that yesterday(June 3rd) was my one year anniversary with LDN too. I am also doing good. My spasms are much better and have been able to cut my spasms medication in half. But I had an MRI and they saw no progression in my disease. That was the first time that they saw no progression. I am so happy about that. Please let us know how your MRI turns out. Good Luck> Marie> ----- Original Message ----- > From: Doherty > LDN chat ; MS watch chat ; Spotlight LDN > Sent: Thursday, June 03, 2004 9:16 PM> Subject: [low dose naltrexone] One year on LDN> Hello fellow MSers!> Just wanted to let you all know that I've been on LDN for exactly one year this Memorial Day weekend. This time last year I could barely walk without pain and stiffness. At one point I couldn't even wear shoes or socks Now there are days when I forget I even have MS. (I also take collodial silver, calcium aep and digestive enzymes). So for those of you just starting LDN please hang in there. It may take a while but I honestly believe in it. I am not 100% healed but am doing so much better. The only problem I have are stilll some numbness in my legs and feet that are still s-l-o-w-l-y subsiding. I plan on getting new MRIs done this summer and will update you all. Please stay positive, LDN works very slowly but it does work. I am praying and thinking of all of you as I read all your messages. > > Your friend,>