low dose naltrexone

Hi everyone,

I am from the MS board and the moderator there mentioned that there was someone here who was using LDN and having good results. I would love to hear about it if they have time to post. Thanks

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Have had relapsing/remitting MS since 10 yrs old. Secondary/progressive since 1995. Baclofen pump since 2008.
Plant your own garden & decorate your own soul instead of waiting for someone to bring you flowers.
Know that you are strong, worthy and can learn & endure.

Hi Popsie,

I have been on LDN since March 28.  The results so far have been good, I have not progressed any since my last update that PALady pulled up, I am holding!  Which means, I am able to do more, the pain level is more tolerable.  This weekend I had friends over for dinner which prior to LDN was impossible.  I sleep better at night!  Most days I am able to take only 3 pain pills vs. 4-5.  I no longer take Tizanidine during the day only 1 at night.  My quality of life IS better!  If you look at the research, LDN has helped many MS and Fibromyalgia and Crohns patients.  Chronic Pain results are now being documented but so far are looking good.

The Pharmacist Marcy told me that even if I do NOT get off PM, in my situation I should consider it a successful treatment!  As I have said in my other posts it is well worth the try, you will know within 2 weeks if it is working, the cost is about $38 per month for 30 caps.  Shipping is free! Dosage is 1 at bedtime.  I started at the 3.0 mg. dose, if I find that it is no longer holding me I can go to a 4.5 mg. dose. 

You can email me directly at edtdoc@aol.com

Patti

Thanks PAlady & Patti,

Thanks for the quick reply. I have just started using low dose Naltrexone (10 days at 3mg) and I have experienced three positives. My left leg which is usually very stiff is much softer at night I can curl up on my side which I could never do before. The other night I woke up cold so I decided to put on some socks. I actually bent over and could reach my feet which I have not been able to do for more than 5 years. This was really exciting for me!!!! This all happens at night I think because you take the naltrexone then and it gives you a spike in the night.

I have not seen any change in the daytime yet, though did think my walking seemed a bit easier. I live in hope of more. It will be a while before I can tell if it has halted the progression as my degeneration is often very subtle. I lost most of my smell & taste last year & my voice has started going so I would like to hang onto anything I have left.

NO negative side effects so far which is great.

Yes, Patti, I also sleep better and dream (nice dreams) a bit more which I enjoy. I will let you all know anything positive.

Hello Gretchen - I love to have a stalker, makes me feel like a celebrity!

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Have had relapsing/remitting MS since 10 yrs old. Secondary/progressive since 1995. Baclofen pump since 2008.
Plant your own garden & decorate your own soul instead of waiting for someone to bring you flowers.
Know that you are strong, worthy and can learn & endure.