Multiple Sclerosis and Low Dose Naltrexone 4

[PaulAandAlethaR]

Stacy, I am so glad you are doing well. My husband had the same quick effects and no side effects. He has been on for 5 years and still doing fantastic. You are right, it is horrible that LDN is not a first line of treatment for MS. It is simply criminal. My husband surfs, works and does as much as he did before he was diagnosed. We are so greatful to have found LDN, and it has stood the test of time. All my best, Aletha

[Masriboy1985]

it started with my whole left left leg going numb starting from lower back then right foot numb, then i got better that i started feeling my left leg and i feel that it is back to normal except the left foot, my right foot is almost feeling normal with partial numbness

11 days ago my right face went numb. prior to that, my left face went numb but not as much as my right one then it started going back to normal. so my left face is back to normal then my right one went numb as if i am durgged

[Masriboy1985]

i personally think these doctors make money from pharmaceutical companies when they get a person started on one of those medications. I found out it would cost me 600$ a month with insurance with only 30% reduction. i found the reduction rate online. All the neurologist said to me was that it would keep the immune system from attacking the myelin. after that i didn't go back to the neurologist and canceled my next appointment.

[Masriboy1985]

on the first day i went to my neurlogist he said i believe you got MS from the symptoms and i would like to talk about treatment.

He gave me four packages of different medications. all were either daily , every other day or weekly shots and very costly.

next week i went to do spinal tab, and draw more blood work

third week he said one of the proteins in spinal tab is positive and other is negative and he would like to talk about choosing a treatment.

[BrytaPlanka]

Hello Stacey! My aunt got something about a year ago that make feel pain all the time, clinch her hands, have back pain, extremly soar and have trouble walking. The doctors doesnt know what it is, but it can be MS. I am going to recommend her to check out this LDN thing! Im sure she will be very happy when she watch your videos! Thanks alot for making them! =)

[Stacy9286]

I am so happy to hear that. I am looking forward now to the days ahead. I am glad to hear you are doing so well

[savingbeauty]

Thanks for the video. LDN is miraculous. From total paralysis attacks to no attacks since 2006. No side effects, no needles and almost no cost!

[Stacy9286]

vern...Thank you for your support but mostly thank you for being such a good friend and a wonderful resource for MS and tysabri info.

[vbeachy]

I am so happy for you Stacy and, can I say? Impressed. Not surprised, I guess...just impressed.

I do regret that Tysabri didn't do anything for you but I am SO GLAD LDN is working great guns for you! Thank you Stacy!

[Stacy9286]

I am so glad my videos are helping and I will keep speaking my mind about the nuerologist

[mwwestiii]

So glad I saw this Stacey! I'm on day four of LDN 1.5 (for two weeks then 3.0 then 4.5) so right behind you. Did Tysabri for 16X to no apparent benefit stopping two months ago. Also started 4AP a month ago which is working well. After seeing your 3.0 results I can't wait. As an MSer for over a decade now, the more I learn about LDN the more it makes me mad that this drug is suppressed by many neuros.