Many of my friends and followers ask me,
"What's it like to live with Multiple Sclerosis?"
"What's it like to live with Multiple Sclerosis?"
That's a trick question because you won't get the same answer
from any two people living with MS.
Most people living with MS have remitting/relapsing MS,
that's me...
good times - bad times, good days - bad days, good hours - bad hours.
Exacerbations followed by periods of wellness or at the very least,
the lessing of symptoms.
MS is a disease in which the immune system eats away at the
protective covering of the nerves.
It is an unpredictable, often disabling disease of the central nervous system
that's disrupts the flow of information within the brain,
and between the brain and the body.
Symptoms range from mild to severe and are different for each person living with MS.
My symptoms are typical, pain being my number one problem.
I also deal with fatigue, weakness, numbness, spasticity, cognitive problems,
bladder problems and problems walking.
It would be awesome if I could transfer the numbness to my areas of pain,
of course, that is not to be.
Two less common MS symptoms I have are seizures and migraines.
Vision problems and optic neuritis are often one of the first symptoms of MS,
and are problems I have dealt with in the past.
There is no cure for Multiple Sclerosis,
but many treatments are available to slow it's progression.
but many treatments are available to slow it's progression.
I treat my MS and all the symptoms I have with medication.
The medications to treat MS work by suppressing the immune system,
therefore making me more susceptible to infections and germs.
The medications to treat MS work by suppressing the immune system,
therefore making me more susceptible to infections and germs.
This pretty jug holds everything I take daily.
The overflow goes here...
The colorful bins are filled to the top...
and
this is the reality of living with a chronic illness.
If you are interested, you can read more about MS here.
The National MS Society has some good information on their website.
I did not turn off comments, but no pity party please.
So many people ask me about my disease,
I wanted to do one informative post for everyone.
My life is not easy - but my blog is for sharing the happy moments,
and there are plenty of those to share.




