Guest guest Posted April 26, 2004 Report Share Posted April 26, 2004 Here goes - I'm completely wheelchair dependent. Balance, what's that? Even with grab bars in the restroom, I have a difficult time getting up, and I can't stand up very straight - abdomen muscles are weak. I am in some type of pain constantly, burning, tingling, numbness, pressurre. At times, it is worse than others but always there. Not complaining. Just stating a fact , and there isn't anything that can be done. I still have tremendous stiffness and spacticity. I'm on Keppra, but it hasn't made that go away. I believe it helps somewhat, but not a whole lot. Sometimes my legs are so weak that I can't make a transfer. I'm trying to figure out if that is the Keppra or what. Yesterday, my legs were so stiff that my 270 lb friend (a man) had a hard time getting my (110 lb) leg to bend! That is stiff! I had Optic Neuritis to begin with that lasted a long time. It's gone now. I think Pregnenolone, DHEA, and bee venom had a part in that. It was gone way before I started LDN. Since starting LDN, bladder urgenct is probably 75% - 80% improved, thankfully. Fatigue is not as bad as it used to be. I still get tired, but not as bad. I'm about at day 170 of LDN (alternate 4.5mg and 3mg w/calcium carbonate filler), and I don't intend to stop now. My mood is better, and that's worth something! I do bee sting therapy too, and I know for certain that the bees give me much needed energy. It seems to mix fine with LDN. YHope this helps! Marcie (PPMS) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2004 Report Share Posted April 26, 2004 Wow, yes everyone, that helps alot, i hope I get to read more on this topic, its still abit early yet, but I must say, Marcie. your situation is so close to mine, minus the pain though. I hope in particular, YOU continue to post your progress on LDN - I uderstand completely about the stiffness and i've had heavy people even sit on my legs trying to bend them to get me into the car - I also dont stand upright, i always lock my knees back to prevent colapsing - much to my physio's horror cause she hates it when i lock my knees, but hey, its not her that falls over everytime i try to do it her way - and isnt it difficult trying to stand AND pull up or down clothing? So, how long exactly have you been on LDN? Friday (keep smiling) , gees we ppl with MS are intelligent arent we? > Here goes - I'm completely wheelchair dependent. Balance, what's that? Even > with grab bars in the restroom, I have a difficult time getting up, and I > can't stand up very straight - abdomen muscles are weak. I am in some type of > pain constantly, burning, tingling, numbness, pressurre. At times, it is worse > than others but always there. Not complaining. Just stating a fact , and > there isn't anything that can be done. I still have tremendous stiffness and > spacticity. I'm on Keppra, but it hasn't made that go away. I believe it helps > somewhat, but not a whole lot. Sometimes my legs are so weak that I can't make > a transfer. I'm trying to figure out if that is the Keppra or what. > Yesterday, my legs were so stiff that my 270 lb friend (a man) had a hard time > getting my (110 lb) leg to bend! That is stiff! > > I had Optic Neuritis to begin with that lasted a long time. It's gone now. > I think Pregnenolone, DHEA, and bee venom had a part in that. It was gone way > before I started LDN. > > Since starting LDN, bladder urgenct is probably 75% - 80% improved, > thankfully. Fatigue is not as bad as it used to be. I still get tired, but not as > bad. I'm about at day 170 of LDN (alternate 4.5mg and 3mg w/calcium carbonate > filler), and I don't intend to stop now. My mood is better, and that's worth > something! > > I do bee sting therapy too, and I know for certain that the bees give me much > needed energy. It seems to mix fine with LDN. > > YHope this helps! > > Marcie (PPMS) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2004 Report Share Posted April 26, 2004 ---My doc faxed the script to Skips for 4.5mg and no one ever mentioned 1.5mg to start out. I found the local pharm was good but I really didn't feel better till I got the meds from Skip--The local pharm was really not a componding pharm. In low dose naltrexone , " Bev " <bbjtwo@c...> wrote: > Hi Steve, > Did you have any problem with Skip wanting you to have just 1.5mg with your > first perception? That's what he told me he would do...I wanted 4.5 so I > went to a local pharmacy...think I should change to Skip's? > > Thanks, > Bev. > > > > > > > > > > > > -------Original Message------- > > From: low dose naltrexone > Date: Monday, April 26, 2004 09:30:08 > low dose naltrexone > Subject: [low dose naltrexone] Re: Physical Disabilities per individual with > MS > > ---I'm on 4.5mg that I get from Skips (Originally had a local > pharmacy compound it but definate differance from Skips), I noticed a > strange sensation (a warm sensation) in my legs which have been numb > for 10 years, after the second day! After the first 2 weeks noticed a > sense of well being, mental contentment, and my symptoms started ever > so slowly to get better. Been on LDN for almost 5 months now and I am > still seeing improvements every week! I't's great! > Steve > > > > > > In low dose naltrexone , YUK713@a... wrote: > > Steve, I would like to know about how long were you > > on LDN when you first noticed that it was working for you? > > And what dose are you on? > > ThankYou > > > > Quote Link to comment Share on other sites More sharing options...
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