
This is important but I have a lot on my mind that seems more important than my teeth. People close to me know that I have been going for Nemours MRI’s and they have shown some scaring on my brain. What has resulted is a meeting with a neurologist who has pointed me in the path of having MS.
After watching some videos and doing some reading about the subject I feel more and more that this is indeed what I have. When I lost the sight in my one eye last spring this was an episode, Optic Noritus. When reading about women who have MS, a lot of them have said this was the trigger that let them know they had MS. Also…woman with MS also experience facial pain and find it difficult to be intimate. Other things that can be effected is the bowls, feeling in the legs and arms, feeling fatigued and tired…and so much more.
See what happens is in the brain we have this casing around our nerves and when you have MS your white blood cells attack the casing and eat away at it…these nerves travel all the way down to your spine and can impact the nerves affecting all parts of the lower body including your legs. These things are answers to so many of the physical concerns I have been having over the last 2 years. Learning this information has made me feel relief because now I know I’m not crazy but at the same time sad because there doesn’t seem to be much to cure it. I know it’s important for me not to get sick because when I am my body will eat away more at the casing around my nerves, it’s complicated to explain but I am just trying to understand it myself.
So all signs are leading to this, often to have a diagnosis you need to get a spinal tap and this might have to happen but we’ll see what this next MRI determines. We want to see if more scaring has flared up..The Neurologist says it is good that I haven’t had another episode since my eye, but I think I have had some small episodes like my leg spazzing in the night and about 2 years ago having horrible pain in my tail bone whenever I sat down …this lasted for almost a month. Back many years ago I had brain fluid behind my eyes and experienced blurriness in my vision and had a lot of headaches…these may or may not have been related but I am getting the results of the MRI I had done back in 2002 to see what showed up then.
I am not sure what to do about things at this point, Some people with MS have had an episode and lost their eye sight forever, some have become unable to walk but trained themselves through therapy to walk again..some have few episodes and it’s not as severe. This is obviously what I am hoping for. I will find out more information from my Neurologist about getting on injections once a week …I would have to do this for the rest of my life but it helps prevent episodes, and the severity of the episodes. I have to do a lot more research and I am sure I will become an expert eventually but I am hoping for a cure so I can feel normal again. I have been reading a lot of forums and people have some really terrible experiences…I know I have Kyle’s undying love and support and I have family who loves me and A God who is always there so I know I will be okay. It’s a lot to think about and it’s something that can be treated and handled so I will just take it one day at a time and see what happens.
SO, this is what is on my mind I, just had to get it off of my mind for a little while. I appreciate everyone’s love and support. You guys Rock and I love you.
1 comment:
Heather, this news is so sad, yet you are so positive. I don't know how you can keep so optimistic - keep it up!
Know that we love you. And what happened in 2002 - I had no idea. You need to let us know what's going on!
We'll be praying for you. I'll also pray your baby teeth will come out without too much hassle. Mouth pain is soooo painful.
Love you girl
Heidi
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