Leg Pain

March 23, 2007

Thank you for this, precious , we are happy that your foot pain is gone.

Sending......love Lea

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~`

Re: Re: Leg Pain

,

I HAD that those burning feet and all my joints.... OUCH

I did the foot baths every other day and took lots of magnesium/calcium/vitamin d in a liquid form..... Plus a good vitamin daily.......

I have good news.......... IT IS GONE!!!!!!!!!!!!

Good Luck

God Bless,

~

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November 30, 2007

Hi Leeka,

Because LDN tends to initially worsen MS symptoms (especially spasticity), the

recommended starting dose is 1.5 mg for the first month, 3 mg the next month,

and then 4.5 mg thereafter.

This site has information about dealing with MS-related spasms:

http://tinyurl.com/3xjll9

For information about treating MS with LDN, visit

http://tinyurl.com/grpm9

For information about dealing with Lyme disease, visit

http://tinyurl.com/2y4n3w

With best wishes,

Dudley Delany

dudley_delany

[low dose naltrexone] leg pain

I started LDN about two weeks ago. For the first few days I had improved

energy, but then

the exacerbation of leg pain with continual cramping kicked in. What has anyone

done to

help with this? How long does it usually last? Since I went off pain meds to

take LDN, i am

just taking supplements and herbs for pain. I suggested to my doctor to reduce

my

presctiption to 1.5 mg for the first month, but he thinks i should just stick it

out until it gets

better. I've started at 3.5 mg. I thought I was having issues with spasticity,

but after a

neurological exam my doctor said I am not and prescribed an anti-depressant and

told me to

just take tylenol. I was on vicodin before the exacerbation and now of course

I'm not taking

it. I'm back in bed and going out of my mind.

I'm interested to know what others have found helpful? Thanks to all in this

group who

helped me find a doctor to prescribe LDN.

Thank you,

leeka

diagnosed with M.S., Transverse Myelitis, Fibromyalgia, C.F.I.D.S., Lyme and

Babesia.

December 1, 2007

Hello Leeka55, This is the first I have responded in this group. I

have been diagnosed with MS in 2000 and started with Copaxone, till

it put me in the hospital and bloated my entire body kept having

relapses and going backwards, then I fired that doc; got another one

that put me on Rebif and tons of pills, relapses kept on and in and

out of the hospital, the flulike symptoms would not stop week after

week, so after doing a lot of research asked him to put me on LDN and

he wouldn't so once again I went in search of another doctor. Finally

found one and got on LDN about a year ago at 3mg. Now my legs are

paining me a lot, my balance is still bad and last week I got the

shingles of course it set in on my worst leg. I totally understand

about the leg pain and added shingle pain to it. Only can take

Tylenol right now and it does not touch the pain. They say do not

take any aspirin with the shingles, dont know why, sorry for rambling

on, cant sleep now and read your email so I thought I would respond.

Sure hope you will feel better soon.

>

> I started LDN about two weeks ago. For the first few days I had

improved energy, but then

> the exacerbation of leg pain with continual cramping kicked in.

What has anyone done to

> help with this? How long does it usually last? Since I went off

pain meds to take LDN, i am

> just taking supplements and herbs for pain. I suggested to my

doctor to reduce my

> presctiption to 1.5 mg for the first month, but he thinks i should

just stick it out until it gets

> better. I've started at 3.5 mg. I thought I was having issues with

spasticity, but after a

> neurological exam my doctor said I am not and prescribed an anti-

depressant and told me to

> just take tylenol. I was on vicodin before the exacerbation and

now of course I'm not taking

> it. I'm back in bed and going out of my mind.

> I'm interested to know what others have found helpful? Thanks to

all in this group who

> helped me find a doctor to prescribe LDN.

> Thank you,

> leeka

> diagnosed with M.S., Transverse Myelitis, Fibromyalgia,

C.F.I.D.S., Lyme and Babesia.

>

December 1, 2007

Hi ,

I suggest you increase your nightly dose of LDN to 4.5 mg.

In regard to your shingles, you may find the following information about

colloidal silver (CS) of interest.

CS, which should not be confused with colloidal silver protein (CSP), is a

natural, non-toxic, broad-spectrum antibiotic that consists entirely of tiny,

submicroscopic particles of silver suspended in distilled water.

CS is colorless, odorless, and tasteless, and in laboratory studies has been

shown to kill more than 600 known pathogens, including viruses, bacteria, and

fungi. Pathogens find it extremely difficult to develop resistance to CS.

CS has been called " the wonder cure that time forgot, " because it is by no means

a new developement. It is sold extensively on the Internet, but is much cheaper

to make your own, which you can do for pennies an ounce.

Some people with shingles claim that taking CS has been of tremendous benefit to

them. See, for example,

http://tinyurl.com/257dag

For more information about colloidal silver, visit

http://tinyurl.com/2fd7xs

There are a number of pain-killers compatible with LDN listed at

http://tinyurl.com/2p57xv

With best wishes,

Dudley Delany

dudley_delany

[low dose naltrexone] Re: leg pain