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Deterioration in MS and LDN...

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Hi, all.....

I just joined the list and have enjoyed reading some of the positive results some of you are getting with LDN.

My mother has had chronic-progressive MS for about 25 years now and has just entered a nursing home. I was wondering if LDN would be of any use to her or if it would be worth a try -- in anyone's opinion? I feel that anything is worth trying at this point. She is very deteriorated, and I don't mean just numbness, spasms, and fatigue. She has no trunk balance, is in bed or a wheel chair (propped up), has no use of her right hand (it's flaccid), has a foley catheter and no bowel control. She is now having problems swallowing. She does have all her mental facilities though, so it is even harder seeing the body going like this. Of course most doctors have given up on her, so I am taking on the quest to bring back or stabilize some of her weak areas. (even looking into apitherapy)

I am researching all I can, and came across the LDN website for the first time yesterday, and thought that it was worth a try.

If any one has an opinion or maybe knows of someone who has severe symptoms like my Mom and has been helped, I'd love to hear them!

Thank you!!

Angie in FL

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