I can't wait to hear about other people's experiences.
I became excited about statins when I read that they help by stopping the inflammatory reaction on the myelin and that it could even regenerate some of the nerves. They even say that in spinal cord injuries, the recovery is better in rats takin statins. My neuro said 'Statins are for rats' but I didn't stop taking it, he had nothing better to offer me....
My name is Jill for those who don't know me. I am in Australia and I take Lipitor 40mg.
I am 30yrs and a bad cholesterol level and my doctor wanted me on Lipitor striaght away but I declined due to my age. My Neuro then spoke up and said that yes she believed it would help me. So I took the leap and am now on 40mg once a day. My doctor believes there is some research that has said that 40mg is the smallest dose that shows its most effective of lowering Cholestoral and for me the 60mag is very expensive. She thought the 10mg would be withdrawan from the market eventually.
I can honestly say that yes it has helped my MS. I feel quite Stable. I have been on it for 4 months now and although I haven't regained anything in the damage I have but for the first time in the last two years I feel "stable" and feel like I can keep it under control. I thought in the end it was a win win situation because it fixed my Cholesterol and it might help my MS. Always up for a drug that does two jobs in one.
I am going on 5 months free of any relapse and aiming 6 months. For those that think it must be my MS Meds - forget it I don't take any of them becuase they just don't agree with me. At lease the Lipitor doesn't have any side effects - well none that I have come across.
Lipitor'sPrescribing Information lists possible side effects including possible liver toxicity, skeletal muscle problems, and adverse drug interactions. I'm posting this because I believe that it's often of benefit for a patient to be aware of possible side effects of any medication they're taking. If you have specific questions on any of the issues discussed in the prescribing information, then you'll likely need to review them with your doctor.noddlebean wrote: At lease the Lipitor doesn't have any side effects - well none that I have come across.
By the way, it's great to hear the positive feedback on Lipitor and that you're finding it beneficial with your MS!
"I started with only 10 mg of Lipitor per day and people noticed that my balance was better. By the time that I took 20 mg, my kids said 'Mom, why don't you come skiing with us. I am now on 60 mg of Lipitor. My liver enzymes are still fine and I have no muscle aches.
It is not a perfect drug but I can't do without it. I like too much the little it has done for me. Carole"
while already. No results on human studies yet have been written up ywt but the studies are on going. I can only say how it helped me ( as described above) and I hope that the effect will only be better with time. Good Luck.
Whether I will admit it or not I guess I have just had 6 months of wellness. Gee thats a first for me.
The only negative thing to say about the Lipitor it can make you more tired or fatiqued - well for me anyway. Apparently theres an enzyme in the body Q10 which converts food into energy and it depleats naturally with age but there has been research thats shown that taking satin drugs speeds the process. I must admit I feel more fatigued than usual but its still better than having a relapse. You can take this enzyme in vitamin form from the pharmacy to counteract the effects. Apparently this enzyme is a good anti-oxident and good for the heart. Anyway apparently its a bit controversal this so my doctor says.
Also I am now wondering about LDN and taking it as well. As both drugs can effect the liver I don't want to push it with the liver. I thought taking the LDN would help with the fatigue side of things and general well being and the Lipitor being a anti-inflamatory will help with keeping the MS in line.
Anyway "on-forward" troops.
I just passed 8 months of relpase free. Well actually I am not sure if I have had one. My legs have been a bit stiff ove rthe last month but I am finding the cold has contributed to that. If it is a relapse its mild enough not to bother me. I myself feel I haven't had one - well not yet anyway - I feel that its keeping it at bay (Lipitor) or keeping it mild. I feel great though - Tried as and the Lipitor contributes to that but I would rather put up with the fatigue any day than some big relapses. I guess I wanna make it to 12 months and then I will be a believer that Statins do help. I feel they are already but I guess I need my own goal to reach. I feel like I have reached one lready.....
In any event, thanks to everyone who is taking statins and posting your status. Please keep it coming. I find the prospect very intriguing and, as I mentioned in another post to this topic, I'm meeting with Dr. Emmanuelle Waubant at the UCSF MS Clinic next week, who is one of the researchers on the trial of statins on folks like myself with CIS. Will let you know what she has to say.
http://www.nature.com/news/2004/040510/ ... 12_pf.html