Huntington Disease Lighthouse Families

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Low Dose Naltrexone - OPINONS

Posted by Dece 
Low Dose Naltrexone - OPINONS
July 14, 2014 03:58AM
Dear All

wonder if you have any knowledge, experience, opinons on this ( by the way Im not looking to endorse or berate this product). I live in Europe and have state health care but this I would have to purchase this medication privately - which is not a problem.

My friends daughter has ME and fybromalgia and uses LDN has done for a few years - however in disussion with my friend she advised this helps AUTOIMMUNE diseases - excuse my ignorance would this be helpful with HD ( my boyfriend is at the early stages (CAG 46) age 43ys, has had signs for about 3 years; balance is off (can still drive), chewing a little laboured, memory impaired, anxiety can be high, hes functiong ie driving, housework, gardening, out with the dogs, etc etc and can focus well on one task at a time.

J is currently on NO medication - waiting to see specialist re this

thanks Dece



Edited 1 time(s). Last edit at 07/14/2014 03:59AM by Dece.
Re: Low Dose Naltrexone - OPINONS
September 11, 2014 09:20AM
I would also like to know about this. My Dr told me to dig around and I haven't really found anything regarding Huntington's. I live in the US and plan on asking my HD Drs but until then has anyone taken this and would you mind sharing you knowledge on it. My mom has MS and I see lots of stuff on that. My father, brother, and myself have HD. Thank you
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