RE: Re: Digest Number 6308

[Guest guest]

Thanks ,

I am taking calcium & magnesium & will increase it as

you suggest. Have eliminated gluten and do monitor my Vit D. Will

also investigate the others.

Trish

From:

low dose naltrexone [mailto:low dose naltrexone ] On

Behalf Of bren_ldn

Sent: Saturday, 21 August 2010 5:21 PM

low dose naltrexone

Subject: [low dose naltrexone] Re: Digest Number 6308

Trish, take 1000mg of magnesium and 1000mg of calcium before bed, L-Taurine.

Also consider getting some magnesium oil and soak feet as per instructions on

jug or google search the magnesium oil. Have your vitamin D level checked. Try

eliminating gluten from your diet and see if that helps also.

, LDN user 7 yrs for chronic progressive MS

=================================================

>

> I have had SPMS for 15 years & RRMS for 45 years and have seen the

following

> Improvements over the last year since taking LDN:

>

> 1 Flexibility of leg, at first only in the middle of the night

> (after taking LDN at 9pm) now all day as well - can kneel for the first

time

> in 15 years

>

> 2 Improved strength and balance of left leg, can stand balanced on

> both legs for the first time in many years (not very well). Combination of

> improved flexibility, strength & balance has lead to improvement in

mobility

>

> 3 Regained 80-90% of smell and taste which I lost nearly completely

> for 3 years

>

> 4 Improved co-ordination of left hand. When I first regained it a

> few months after I started taking LDN I could type perfectly. Then I lost

> it due to allergic reaction to LDN & now I have the improved co-

ordination

> but weakness of hand negatively impacts on the co-ordination. Little &

ring

> finger the weakest.

>

> 5 Have totally regained normal speaking - I had been gradually

> losing both the strength/projection of my voice for the last 2 years.

> Raising my voice and even talking was often an effort - now I am told not

to

> talk so loud!

>

> 6 Choking - much, much improved had hardly any in last few months

>

> 7 Pins & needles and flares of pain like being jabbed with a needle

> - none in last five months

>

> 8 No colds/flu & no bouts of sinus (which used to be a constant

> problem & lead to exacerbation of MS - LDN boosts immune system)

>

> 9 Bladder improved

>

> 10 Feel really good/cheerful (LDN releases endorphins)

>

>

>

> BUT I have had to stop LDN because of severe spasms keeping me awake all

> night. I have been off LDN for a month (still spasming) and I have started

> LOSING some of the benefits. The following has happened - flexibility

&

> mobility much less, post nasal drip returned, some choking, loss some of

> sense of smell, pain flares in toesL

>

>

>

> Two months later I am still spasming but am taking 2.00 mg of LDN

> transdermally once a week which stops the sinus, choking and pain flares.

> It has also proved the spasms are caused by allergy to LDN as the night I

> take it they are much, much worse. As I have been dealing with multiple

> allergies for years I know that as long as I persist I will deal with this

> one too.

>

>

>

> LDN is magic just persist & be patient & you will see it too BUT

if you are

> at all allergic I would strongly recommend you take it transdermally -

> transdermal has benefits too :

>

> 1 immediate absorption

>

> 2 do not need to take it with food

>

> 3 easier to adjust the dose up or down as you need

>

>

>

>

>

> All the best

>

> Trish

>

>

>

>

>

>

>

>

>

> I have been taking LDN for about 2mth now and started on a low dose of

1.5mg

> and now I'm taking 3.0 mg and I think it will be @that dose for a while. I

> have very vivid dreams everyday with LDN. Is it doing anything for MS, not

> sure. Any feedback is greatly appreciated.

>

> Sent from my BlackBerry device on the Wireless Network

>

> _____

>