Re: Marcie where in West Texas do you call home?

[Guest guest]

Hi!

I'm just outside of Slaton, which is about 15 miles SE of Lubbock! Right on your way to Amarillo! We did have a 'White Christmas', but I can't say that I liked it. Makes for a big mess as it melts! Funny how it seemed the coldest weather was in a line from Hobbs, NM to Plains and on east towards Snyder. Would have thought that the Panhandle would have been colder.

LDN has been good for me. I have seen some improvement, and considering how progressed I am, I'll take whatever I can get! Bladder issues are the most improved. I sleep much better. Not as much numbness and tingling. I do take Keppra for spacticity. My legs are so very stiff. I did Avonex for 2 years in the beginning. It did nothing for me. Baclofen didn't help me, and I didn't/don't want to risk losing ang strength. Detrol didn't help my bladder issues. I take good vitamin/minerals, a couple of supplements, LDN & Keppra. That's it. I try to eat healthy. TRY! Easier said than done! I was diagnosed in 1997. I have been in a wheelchair since Nov '99. No fun!

I hope has good results with LDN. It's, in my opinion, what people should try first thing! Keep us posted!

Marcie

In a message dated 12/27/2004 10:13:39 AM Central Standard Time, pigeon2003@... writes:

Hi Marcie, saw your post about being in West Texas. I am the mother of a daughter living in CA with MS and we are waiting for her consultation with Dr. on the 30th for a script of ldn. I am in Midland, Texas, but we lived for a short time in Amarillo. How long have you had MS and what have you tried and how is the ldn working for you? We are keeping our fingers crossed that it will help our daughter, . Hope you had a good Christmas; it was very cold here, and we almost had a "white" holiday.

[Guest guest]

Hi ,

Raelene and Friday are both in Australia too. They both are on LDN. Just be sure to take info from the low dose naltrexone.org website. I wish you lots of good luck! Hang in there!

Marcie

In a message dated 12/28/2004 6:59:44 AM Central Standard Time, monica_wall2000@... writes:

hi marcie! my name is monica and i have ms ive had it for 5yrs now, in in relaps, remitting ms, i heard so much about neltrexone that im eager 2 try it, because i am a new comer 2 this drg i dont know much about it , ive done a bit of research, but im still searching 4 more. i live in perth western australia and at the moment the holiday session mucks all the drs and hospitals around until everything opens up again in another weeks time, which is a bumer, all i can do at the moment is get my info on it, so if u now anything i would aprechate the info, thank-u 4 your time monica