Multiple Sclerosis is an
autoimmune disease of the central nervous system. What this means is that the
person’s own immune cells (white blood cells) are attacking the nerves of the brain and spinal column. MS causes inflammatory demyelination: it specifically attacks the myelin (protective coating) surrounding
the nerves and causes inflammation. Without the myelin, these weakened nerves
cannot carry messages well, and can even break. Basically, any function in the
body that is controlled by the nerves (which is all of them) can be affected.
Let’s try to break this down and explain a little more. The first question that came to my mind is “How?” The
blood brain barrier’s job is to keep larger cells from getting into the brain.
The cell walls of the blood vessels in the CNS are tighter than elsewhere in the body.
This means that there has to be a breakdown of the BBB in order for the large immune cells to get past it. I’m not quite sure yet what causes this to happen.
The second question is
“Why?” The immune cells develop along with the other cells of the
body. All cells have receptors (antigens) on them so that the immune cells will
know that they belong to that body and are not an invader. So, why are they picking
on myelin? It is thought that these cells may develop after the BBB has already
formed, so the immune cells don’t get the chance to become acquainted with them.
The immune cells, specifically the T-cells, are very good at their job. Not
only do they go in and destroy the “invaders” that they find, but they also call in reinforcements. Their call signals, called cytokines, help with both of these functions.
So, we have immune cells
where they’re not supposed to be and they’re attacking cells just because they don’t know them. But, why is this causing problems all-over the body? The answer
is in the way the nerves work. Think of nerves like telephone wires. A message is put in at one end and carried to the other. This
works in both directions, just using parallel wires. If there is interference
in one wire, it shorts-out. You may not be able to hear the person on the other
end, but they could hear you just fine. The body works the same way. The brain literally “short-circuits” and it either prevents the brain from transmitting or
receiving messages. The areas that have been attacked are called plaques or lesions,
and on an MRI scan they look like little circles that have been whited-out.
The good thing is that
the effects of this damage need not be permanent. Steroids can be administered
to quiet the immune response. The other drugs used to treat MS also work to activate
cells that will stop this response and try to strengthen the BBB. Some of the
myelin will repair its self, a process which can be aided by dietary changes or supplements.
The only thing that cannot be helped is broken nerves. Nerve cells don’t
usually grow back. Over time, multiple broken nerves will curl-up on themselves
and give the appearance of brain atrophy (shrinkage).
MS attacks women compared
to men at a ratio of 4 to 1. This could be due to a difference in hormone levels,
which is being investigated. Another reason for this belief is because of what
happens during pregnancy. For women with MS and some other autoimmune diseases,
the progression of the disease stops while pregnant. Of course, any damage that
has already happened will remain, but there will be no further attacks. This
is really good, since you wouldn’t want to be on the medication then anyways.
The down-side to this is that shortly after delivery, about two weeks later, the disease comes back full-force. This can be delayed or slowed my breast feeding, but not completely.
There are 5 primary drugs
on the market to treat MS. Some work slightly different from the others, and
they all carry their own side-effects. There are new drugs in clinical trials
at the moment, including some that can be taken orally. This is great news for
two reasons: 1) All of the current therapies are given via injection, either intramuscular (hurts like heck!), subcutaneous
(feels like a bee sting), or intravenous (IV-enough said); and 2) Over time the body developes an immunity to the medicine,
or the person may have a reaction to it, or it might just not work for that person.
Anyway you look at it, new treatment options are always good…and this makes all of us needle-phobics in the world
rejoice! Not to mention that the current “last” option is either
steroids in combination with one of the other drugs, or chemotherapy. I, for
one, prefer to not gain a grotesque amount of weight or lose anymore of my hair!
To sum all this up is one
statement, “MS is devastating, dehabilitating, and depressing…but there is always hope.”
To learn what I've dealt with personally,
read "My Story".