My MS symptoms are somewhat mild. My number one symptom is fatigue and the majority of people with MS will tell you the same. This is not just your normal fatigue brought on by not getting enough sleep or after working a long hard day. This fatigue is called lassitude or MS fatigue. I also experience numbness in my right foot near my toes and body aches from head to toe. Mentally I have brain fog which is exactly how it sounds. I have a lot of lesions in my brain and it affects my memory, cognitive skills such as writing and my mood.
Lately I have been noticing sharp pains in my neck and spine. It feels like my nerves are backfiring and it hurts like hedoubleL. Thankfully the pain doesn't last very long and it's sporadic.
I know and feel that I am truly blessed. I have access to treatments that weren't availble 15 years ago. I used to tell my family and friends that if I had to choose between MS and other diseases such as cancer or lupus or sickle cell anemia, then MS would be my choice. God knows what He is doing and He has me in His hands. As long as I stay close to God, I will always be ok. He gives me strength that causes some people to wonder about me? People used to say, "I don't know how you do it", and I tell them that it's the God in me. Apart from Him then MS would probably have me feeling sorry for myself. But there are too many blessings in my life to focus on this disease and let it have me down all the time.
Friday, December 31, 2010
Monday, December 27, 2010
I have a question for my viewers. "When a person parks in a space marked for "Handicap", what should that person look like? Should they be in a wheelchair or have a cane? Is it ok if you cannot tell by looking at them or watching them that they be able to use that spot w/o you doing a triple take? Disabled parking is not just for the obvious. I have included a link to the DMV criteria for disabled parking in my state. NV DMV Disabled Parking I encourage people to read requirements by the DMV in order to receive a handicap placard or license plate. You cannot tell by looking at me that I am approved to use handicapped parking but I am and I do. At first, I actually felt bad and worried about what people would think of me. I don't always feel the need for it and on days like that , I use regular parking spots. I truly felt like I needed to explain myself or try to appear more visually impaired. I finally got over that because guess what, if a person is ignorant enough to stare at you like you're doing something wrong, you will probably end up in an argument with them by asking them if they have a problem. And for what? I know better than to stress myself out since for most people, ignorance is bliss anyways. So I have decided to keep it movin and go about my business. Then of course there are the people that know you a tiny bit so they feel comfortable asking you why you are parking there. I still haven't learned how to respond to that question w/o saying, "It's none of your business or why do you ask?" Cause if you knew me that well then you wouldn't need to ask me that question. I know for the most part that curiosity can cause people to forget their manners. If you are one of those people then I forgive you. Just take the time to educate yourself every now and then and maybe you won't need to know why someone is parking in a "Handicapped" spot when they are not in a wheelchair or walking with a cane. Let's all try not to be so simple minded.
Sunday, December 12, 2010
When I was diagnosed with Multiple Sclerosis at the end of 2007, my family was more afraid than I was. None of us knew anything about the disease or what the prognosis would be. I knew that my chance of having the disease was 50% by then because I started having problems about 9 months before my diagnosis. During one trip to the emergency room a doctor mentioned that she believed I might have MS. Once I heard that word, I went home and did as much research as I could on the subject. The only thing I knew about MS before that was that Montel Williams had it but I never gave it much thought until there was a possibility that I might have it myself. The first thing I wanted to know is, "Will this kill me?" I was very relieved to find out that most people with MS go on to lead a somewhat normal life and no it would not "kill" me. That was a relief. I am blessed to have a great circle of family and friends that support me. My husband and 3 daughters even learned how to administer my nightly shot for the first 6 months but the shots weren't keeping the disease at bay so I now receive my treatments via IV at an infusion center once a month. This approach is more aggressive because as an African American, MS is more aggressive for us. I will post more about that at a later time. My main symptoms are numbness in my right foot and periodically other areas below the waist, fatigue (more about that later as well), brain fog and muscle aches. This disease is teaching me a lot about life in general. I believe that God is using me in one of His mysterious ways to shed as much light as I can to as many people as I can reach and bring Him glory in the process. Not only that but "What doesn't kill you only makes you stronger right?" I believe that without a doubt just as surely as I know that there is a God in heaven who loves me.