Re: Dr. Bihari to write forward to Google LDN!

[Guest guest]

-I have been engulfed in this website for 6 solid days!!! HOWEVER I

need to know if for a fact there have been scleroderma users on LDN??

I have the more serious diffuse sclerdoerma. I have had one treatment

of chemo and NEED to know if I should start this LDN ASAP.

Cant someone take some time off the voting page and give me some

detailed concrete feedback regarding scleroderma? Can someone out

there save my life too so that afterwards I can spread the word ouh

here in Montreal Canada?> I do have a large network of key people

that could campaign LDN> But before I let the cat out of the bag, I

want to kno if my serious illness had been tested by others??

Please Please email me at MTLCUTE@AOL>COM

thank you

Marla

mtlcute@...

-- In low dose naltrexone , " Art Hansen " <rtee54@...>

wrote:

>

> Yesterday Dr. Bihari Called me. He had read the entire book and was

> thrilled with it. I asked him to please send any corrections to

> anything he thought was off, but he said he hadn't seen anything

> wrong.

>

> I asked if he'd be willing to write a 10 page or so summary of the

> current state of LDN knowledge to put at the beginning of the

appendix

> and he agreed to do so.

>

> He also honored me by agreeing to write a forward to the book.

>

> This is only the beginning, my friends. This is the year that LDN is

> going to break through to the public at large and really start

making

> a difference to the millions of suffering people it can help.

>

> Again, thank you all for your support and your help. Together we're

> going to make this happen.

>

> Warmest,

>

> Joe

>

> PS could one of you please post this notice to the low dose naltrexone

> group? Thanks.

>

[Guest guest]

In low dose naltrexone , "Conni Lawrence" <summerwind1@...> wrote:I

have scleroderma, crest syndrome and have been on ldn for almost 15

months. I also have sjrogrens, and fibromyalgia. I have to say that

within a week of starting ldn, I felt like: I had my life back, my body

was working correctly for the first time in a long time, and my fatigue

and pain were minimal. I work with many people that know me well, and

everyone wasnoticing how much better I was. I have a list I made

about a page long of all the things that were better and I need to find

that. > >> > Yesterday Dr. Bihari Called me. He had read the entire book and was> > thrilled with it. I asked him to please send any corrections to> > anything he thought was off, but he said he hadn't seen anything > > wrong.> > > > I asked if he'd be willing to write a 10 page or so summary of the> > current state of LDN knowledge to put at the beginning of the > appendix> > and he agreed to do so.> > > > He also honored me by agreeing to write a forward to the book.> > > > This is only the beginning, my friends. This is the year that LDN is> > going to break through to the public at large and really start > making> > a difference to the millions of suffering people it can help.> > > > Again, thank you all for your support and your help. Together we're> > going to make this happen.> > > > Warmest,> > > > Joe> > > > PS could one of you please post this notice to the low dose naltrexone> > group? Thanks.> >>

[Guest guest]

Dear Marla,

I just sent you some info on LDN and I forwarded what I had saved from our chat site regarding scleroderma. Please let me know if you have any questions or need any additional information.

My e-mail address is Aletha@...

My best, Aletha

[Guest guest]

Go here and read this about scleroderma:

http://tinyurl.com/6uqz88

In fact search 's entire site for scleroderma. Many stories and

info.

On this board if you'll performa search you'll come up with over 90

posts pertaining to scleroderma.

Art

--

>

> -I have been engulfed in this website for 6 solid days!!! HOWEVER I

> need to know if for a fact there have been scleroderma users on

LDN??

> I have the more serious diffuse sclerdoerma. I have had one

treatment

> of chemo and NEED to know if I should start this LDN ASAP.

>

> Cant someone take some time off the voting page and give me some

> detailed concrete feedback regarding scleroderma? Can someone out

> there save my life too so that afterwards I can spread the word ouh

> here in Montreal Canada?> I do have a large network of key people

> that could campaign LDN> But before I let the cat out of the bag, I

> want to kno if my serious illness had been tested by others??

> Please Please email me at MTLCUTE@AOL>COM

> thank you

> Marla

> mtlcute@...

[Guest guest]

On this site there are over 90 posts with scleroderma in the subject

line or in the post.

http://tinyurl.com/9q4rp5

If you'll go to 's site use the search feature which is near

the bottom of the home page and you should come up with a bunch of

stuff. Otherwise this is all the help I can offer you.

http://ldn.proboards3.com/index.cgi

Scleroderma is considered an autoimmune disease so LDN should be of

some benefit to you.

Art

--

>

> Hello Art;

> ? I was so happy to see your response. When i went to the site it

is the article from only Connie. There are not 90 testimonials.Please

write me back i I am wrong.

> Thanks Marla

> mtlcute@...

>

>

> [low dose naltrexone] Re: Dr. Bihari to write forward to

Google LDN!

>

>

>

>

>

>

> Go here and read this about scleroderma:

>

> http://tinyurl.com/6uqz88

>

> In fact search 's entire site for scleroderma. Many stories

and

> info.

>

> On this board if you'll performa search you'll come up with over 90

> posts pertaining to scleroderma.

>

> Art

> --

>

> >

> > -I have been engulfed in this website for 6 solid days!!! HOWEVER

I

> > need to know if for a fact there have been scleroderma users on

> LDN??

> > I have the more serious diffuse sclerdoerma. I have had one

> treatment

> > of chemo and NEED to know if I should start this LDN ASAP.

> >

> > Cant someone take some time off the voting page and give me some

> > detailed concrete feedback regarding scleroderma? Can someone out

> > there save my life too so that afterwards I can spread the word

ouh

> > here in Montreal Canada?> I do have a large network of key people

> > that could campaign LDN> But before I let the cat out of the bag,

I

> > want to kno if my serious illness had been tested by others??

> > Please Please email me at MTLCUTE@AOL>COM

> > thank you

> > Marla

> > mtlcute@

>