off topic

[Guest guest]

Hi Dudley,

LOOKING GOOD!! You look great and do not look 69 years old!!

Best,

[Guest guest]

Nice to have face, with the name!

Have a Happy and Healthy Day,

Kopera M.H.

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________________________________

To: cancercure ; germanfriends ;

LDN_Users ; mscured ; nursing2

Sent: Saturday, September 12, 2009 9:12:32 AM

Subject: Off Topic

Hi Everyone,

I was at a luncheon a few days ago, and someone with a digital camera snapped

the enclosed photo of me. Thought you might care to see it.

With best wishes,

Dudley Delany

http://profiles. yahoo.com/ dudley_delany

[Guest guest]

>

> Hi Everyone,

>

> I was at a luncheon a few days ago, and someone with a digital camera snapped

the enclosed photo of me. Thought you might care to see it.

>

> With best wishes,

>

> Dudley Delany

>

> http://profiles.yahoo.com/dudley_delany

Who's that handsome fella?

[Guest guest]

I know you can't use these 2 medicines together, but has anyone tried cell cept?

f you have what was your experience with it. I have been on ldn 3.0 mg for 3

years and my mri's continue to get worse, and my disability progresses. I have

SPMS 5 years.

My nuero said we have to stop the progression.

any words of wisdom? thanks

keith

[Guest guest]

, in addition to diet, supplements and LDN, I get the Dr. Klenner Protocol

Vit. B1 and Liver Injections. I don't know WHAT kind of MS I have, as I only

went to the neuro once for diagnosis. Didn't see what else he could do for me,

since I wouldn't take drugs, so I just never went back.

I was dx in Sept. 07 (at 53). I did start going downhill initially, so I

presume I have PP, like my sister a had. But since diet and everything

else, things have started to turn around. Right now I am feeling good. I

stopped using my cane, altho I still ride the electric carts at Walmart (I think

I just enjoy riding around rather than walking those big stores). I am back to

working (retail) 11 hours a week. The tremor in my hand is now negligible.

I don't know to what to attribute it, but I don't really care, either. As long

as something is working.

One thing I think did make a difference was when I shifted all my supplements to

incorporate everything I could think of for circulation (based on the CCSVI

theory). My arms used to go numb when I slept; since my supplement changes 3

mos ago, this has stopped (yippee!).

If you want to email me off-list for info about Dr. Klenner protocol, or the

supplements I take, please feel free.

Hang in there!

Beverly

>

> I know you can't use these 2 medicines together, but has anyone tried cell

cept? f you have what was your experience with it. I have been on ldn 3.0 mg for

3 years and my mri's continue to get worse, and my disability progresses. I have

SPMS 5 years.

> My nuero said we have to stop the progression.

> any words of wisdom? thanks

> keith

>