As strange as it might sound. Leprosy, tuberculosis, psoriasis, type 1 diabetes and MS might have one common fact — clofazimine. Clofazimine has been on the market for more than 100 years. Some brilliant people at Johns Hopkins have found out that clofazimine has some kind of interaction in our immune system. It would be too technical to go further into detail — but you can read more about this at the sciencedaily website.
Where do we go from here? All I can say on this matter is that I do believe that with all the good news I am reading tthese days that our live will get better. They will find the one medication that will be able to cure MS at one point. We just have to hang in there and hope that the ms cure will come in time for us to have a positive outcome, as well.
Try to have a positive outlook, as well. To me — every day I read about new studies in MS research is a good day. All we have to do is wait for the one big finding that will help us all. And who knows — this day might come quicker than we think.
So cross your fingers and take care.
This morning I woke up to this great news on my viigo blackberry newsreader. I thought I might share this inforamtion here on my blog so more and more people will hear about it.
The BBC reported today that MS stem-cell treatment as a ‘success’. A small study had been done to see whether stem cells could be a way to help people with MS. The study suggested two things
1.)stem-cell transplats may control MS symptoms
2.)and even better — may even reverse multiple sclerosis symptoms
Of course, there is always the ethic aspects and some people will always oppose stem cell research etc. But then there are people who believe that there is nothing wrong with stem-cell research and that we should do everything we can in order to save people’s life. And if stem-cells can be used to make our life better, than I wouldn’t mind these kind of treatments.
If you are interested in reading the rest of the article check out this link MS stem-cell treatment success.
When I read this post today on the internet I became very excited. Knowing that there might be a pill that could replace daily or weekly injections to decrease the amount of relapses sounds just great. I hate those shots — in fact this is the reason why I stopped taking them 10 months ago. And knoock on wood I had no major problems every stopping the medicine. But if I could have the option of taking a pill instead of the injection I would be more likely go back on my medication.
But what exactly is Cladribine. Cladribine is commonly used for leukemic reticuloendotheliosis. This mediciation is not given over a long period of time. So this could be the downfall for Cladribine as far as MS is concerned. We all know that MS will stick with us for the rest of our life. And this could mean that we will have to take Cladribine for a much longer period of time. And how about the side effects? Cancer treatment is known for heavy side effects.
But we should consider all aspects of this. Not only the side effects but also the (hopefully, positivs outcome. If taking Cladribine might cause me to be a little more fatigue but I won’t have to end up in a wheelchair than I would be very happy to try this pill. I guess, it all depends on what we would like to do with our lives. Even if it would mean that we would only get 5 or 10 more years good life without the use of a wheelchair or a walker. These 5 or 10 years of possible fatigue are better than what could happen to us if we wouldn’t feel that
Maybe this will be what we are all looking for.
Merck: New pill may work for MS
Thank you Merck
There is a big chance that the Wii Fit is not as good as people say it is. But all I can say on this matter is the fact that I have been using the Wii Fit for almost 6 months on a daily basis. I love my daily exercise. Of course, i have read the horror stories about the Wii Knee. But who cares? And who believes in this anyway.
Personally, I see the Wii Fit as a tool to keep me
3.) in a good mood
This is all I am asking for. And this is all I am getting. So why don’t you try it yourself?
Personally, I don’t write a Multiple Sclerosis log myself as I don’t always want to be reminded if my MS. But I can see that it helps people who have more symptoms. And for these patients it is essential to know what is going on, why it is going on, what has been tried to resolve the problem and was it successful or not. These are the kinds of information your neurologist needs from you if you see him or her at the next appointment. And I know that once I will have more problems myself — I will start the journal. No question about that.
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