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Jennifer Gerics
- LDN
Here's a post from someone using LDN for MS (she's responding to someone in the "MS Overview" discussion):
It has been a while since I've written on this site. I'm the angry daughter of a progressive MS patient who was diagnosed with MS myself. I am really sorry to hear about your sister and remember the frustration. I can honestly say that I truly understand what it feels like now. When you cannot provide for yourself and have to count on other people to do basic tasks for you it is NO FUN! You feel like a burden to those you love and useless to society.
I have been in your position and now her position. I know that trying to be patient with her is an over used statement for you, but that is my advise.
I also want to let everyone know that I have started LDN treatment. AND.........I FEEL GREAT!!!!!!!!!!!!!!!
No more spasams, numbness or fatigue! You would be crazy not to try this treatment. After all, what do you have to loose?
Before I started taking LDN, I was on several medications:
-Trazadone
-Welbutrin
-Rebif
-Immitrex
-Ritalin
-Flexril
-Topamax
and also tylenol or motrin for pain
After I started taking LDN, I no longer take ANY of these medications. It is true that medications have side affects. Maybe some of the meds your sister is taking is making her do and feel the things she is. I know that I was unhappy with the side effects I experienced with the meds I was on. I hope everything works out for you, as I am sure that it will.
On a lighter note, I am proud to be another LDN success story. Hopefully my path with MS will not follow my relatives. I can only cross my fingers and take every day as it comes. With LDN, I feel like I am able to have a more positive outlook for my future.
Wilburn in Ohio
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