Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I have many lesions showing up on my MRIs in my brain and one "suspicious" lesion on my spinal cord. The spinal cord lesion is what prompted them to do the MRI of my brain. I have no symptoms that involve my lower extremities at all. My issues are with balance, vision and my upper extremities. So far, none of my issues are debilitating and I will do my best to keep it that way. I am taking one of the CRABS, but am working with another doctor, in another town to get started with LDN, because what I have read about it is very promising. However, not promising enough for my neurologist's comfort.
I agree with Larrymontana's statement, "Doctors would love it if they could identify the extent of your disability from an MRI." This nurse would love that, too. It sure would make treatment and prognosis a whole lot easier to figure out for myself and others.
Please try to stay as positive as you possibly can. Take care of yourself in the way you know how and with the advice of those you trust to advise you. I do realize that is much easier said than done, but it is very possible. There are many people here on this site that will be there when you want and/or need!
Taking one of the CRAB drugs should reduce future damage, (progression), but they don't usually help with the symptoms. Sometimes the CRAB drugs help set the body in motion for healing, and it is possible for symptoms to decrease. I have had slight improvement with a few of mine, but that could very well be a part of the relapsing and remitting process. No one really knows for sure. Once I get started with LDN, I'll try to share how it goes, but LarryLDN and Larrymontana both already have first hand information. LarryLDN has years of journals that share excellent information for anyone wanting to read it.
There is much known and little known about MS. Until the scientific world discovers something they deem provable and beneficial through their methods, we all have to go through "trial and error," with or without them. It is not an easy road, but it can be navigated. I have found DS to be a wonderful source of support and information. Just be careful and as safe as possible with the trial and error you choose.
Take care and good luck with whatever you choose to do to help yourself. Dont forget we are all here!
Rebecca
http://members.tripod.com/~ThJuland/axon-disability.html
Since we don;t have any hard evidence of exact correlations, we have to go on common sense much of the time.
If you have a relapse that included a lesion in a specific area and have lost functions where that are of the brain controls, than its hard to deny any correlation at all.
I do think that it is more common when there is actual axon loss, and or the brain cells are dead. Hope that made sense!
I made some major spelling errors though and wish I could edit! LOL
I would be happy to be corrected (with some Journal citation). Fact is that you could have one smal barely noticable lesion and be severly disabled or have a brain that looks like a Christmas tree and be in great shape.
Yes I've heard that some Docs believe lesions on your spine are responsible for motor difficulties but mine are in my brain and throw off my balance. And even given that I don't believe there is any published study that draws a corresspondence between location and or size of lesions and disability.
Much of what we as patients believe is based on common sense, so I wouldn't only rely on medical journal, as because just as something hasn't beenfully proven, much has also not been DISproven completely either - we are all still learning.
I do believe that lesions certainly CAN correlate, as I said before.
I will never believe that brain damage would not affect our abilities...
For various pains we get, do not discount the over-the-counter patches they have everywhere now. The menthol is quite effective in masking the one pain that is worse.
I use ice to help some things and less frequently, heat. Aleve has been a big help to me--especially taken three time a day. I try and stay positive by helping others. Good luck! Jane in Indiana
you can have minor flare with many lesions
sometimes i wonder--whats the use of a mri-
but guess they are necessary--i am in a bad flare since nov--my recent mri showed no active lesions
but guess what did show up? A STROKE! oh my! problems problems PROBLEMS!
Get a second opinion.