Muscular Dystrophy

[Guest guest]

In my opinion, What would it hurt to try.

My sister-in-law has MD in her family.

Her sister has it and her brother died from it.

She could be a carrier so she and my brother

decided not to have children.

So like I said at the top, what would it hurt

and also,You'll never know till you try.

It's just like MS, You never know if something

will work until you try.

Good Luck.

ADJ

[Guest guest]

Dr. Bihari reports trying LDN on 12 kids. He got good results on 6

and

no results on 6. Dr. Gluck says that if kids are on steriods they

can't

take LDN since they work against each other.

I would suggest trying 1.5 mg/day first and progress up to 3.0 mg/day

after a few weeks and then 4.5 mg/day if there is no reduction of

symptoms. It has been my experience that you can take too much LDN

and

the symptoms will become worse rather than better.

If you do decide on trying LDN, please please report your results.

Arnold

[Guest guest]

Hi:

Does someone have Dr. Gluck's email address? I want to pick his brain

on LDN treating muscular dysrophy.

Dr. Pelofsky

[Guest guest]

ALS is not generally regarded as an auto immune disease either but I

know quite a few people deriving a lot of benefit from using LDN for

their ALS. Given how cheap and safe it is I'd definitely be using it!!

Even if it doesn't directly help the MD it was almost certainly give an

improvement in general wellbeing.

Aletha Wittmann wrote:

> As far as I know LDN would not be helpful for MD. Shame.

>

> * [low dose naltrexone] Muscular dystrophy

>

> Dear Group

>

> Can LDN be used for Muscular Dystrophy or is it not a auto immune

> disease. Would appreciate clarity on this.

>

> Regards

> Martie Hanekom

>

>