"Who has believed our report?
And to whom has the arm of the Lord been revealed?" Isaiah 53:1
Brain Fog. What?
Get link
Facebook
X
Pinterest
Email
Other Apps
I experience this one every day. I guess this is my
new way of living. I haven't done any research, all I know is how I
feel. Brain fog played a major factor in being unable to work.
The Gift of a Relationship Ruth and I have chosen to put our trust in Jesus not man. When people are faced with a life time of hardships, many will turn to religion, but religion is not the answer, a relationship with Jesus is. I believe that we must develop a relationship with our creator. Religion only gives us guidelines to live by, because religion in no more than rules and regulations to live by. A relationship on the other hand will occupy every part of your being. Relationships are intimate, up close and personal. An intimate relationship with Jesus is no differences from what we have with other closest friends and family members. The only difference is the way we get to know Jesus; through his word ( the Bible ). He already knows us: “ I knew you before I formed you in your mother’s womb, before you were born I set you apart ” Jeremiah 1:5 . In life people can and often do let us down, things change. Someone might say their willing but when it comes time...
I believe that prayer is a vital part of a successful marriage, because I invite Christ into my marriage to shape each of us as He desires. It is not up to me to change and shape my husband, it is up to Christ, after all He knows so much better than I do. I believe I can bring good to my husband through prayer. Prayer for his integrity, his strengths, his weaknesses, his walk, his work – for every aspect of His life.
I don’t always feel like smiling, or doing the things I know to be right. I don’t always feel peace & joy. There are moments I feel like crying, I feel like I’m about to break or my earth is about to shake. The harder I try the worse it gets, and failure is on my back. I had rough mornings in which turns into rough days which ends as a rough week. But in those times, I press on. What and how I’m feeling is a part of living life with MS, but I won’t allow it to STOP MY LIFE. I refuse to park here. I’m going to release these feelings back to the pit of hell. I won’t always feel and sometimes I don’t look like I’m fearfully and wonderfully made, BUT I AM…… “I praise you because I am fearfully and wonderfully made; your works are wonderful, I know that full well”. Psalm 139:14
MS Itch has me feeling like I'm in "The Itchy & Scratchy Show". MS is Itchy & I'm Scratchy! I was reading this article about the MS itch. I don't know what site I was on. My point is, I would not call it an itch. My experience is, it feels more like a burning sensation. So uncomfortable that it feels as if someone is holding a match to my skin. Yes, I scratch because it's bothersome and I want the feeling to go away. I only get this feeling in my legs and feet. One day I felt so uncomfortable that I told myself I was going to cut my legs off & call myself shorty. 😊 I have to make lite of it all because I do not want to be moved by my circumstances. I do have some relief; I use medicated cream. The cream helps for about 6-8 hours or so. “The angel of the Lord encamps all around those who fear Him, And delivers them. Oh, taste and see that the Lord is good.” Psalm 34:7...
I was watching the news in reference to the Government shutdown. This lady was on there crying because with no pay, her and her son will be homeless. Point being, it is a lesson in it for us all. In one way or the other we will be if not already effected. Lesson being, God is my Provider; it's all just stuff. God wants all of us to lean & depend upon Him. "For kings and all those in authority, that we may live peaceful and quiet lives in all godliness and holiness. This is good, and pleases God our Savior, who wants all people to be saved and to come to a knowledge of the truth." 1st Timothy 2:2-4
Early in the diagnosis of MS a friend told me that she was having a problem with button up shirts and I didn't understand so I just listened to her story. My point is, today, I GET IT! It takes me 30 minutes to button my shirt; 45 or so just to zipen my coat. I can't be that person that says, I can't do it. I have to try!
Timeline speaks about PPMS & exercises that can be done to increase cognitive behavior skills. However as I said before, I feel that disease is disease. MS or something else. The activities that are suggested: Stay act ive Get adequate sleep Play memory games Write Play puzzle/problem solving activities Get organized Read daily Check medications Counseling Timeline also says that lifestyle choices have big effect on a person’s condition. I try to do all activities that’s suggested. · I’m not as active as I would like to be. If you have a disease that effects your mobility, how active can one be? · Sleep-YES · Every day I play games and/or use my problem solving skills. · Write-I try to blog every day, but I can’t write with a pen/pencil. Handshaking make for bad penmanship. ...
After receiving a small glimpse into the diversity of others diagnosed with MS; I realized one thing, MS does not discriminate. The fury of MS can be unleashed on anybody; at anytime, no matter who you are or your walk in life. After analyzing it all, my first thought was WOW. I also thought about Mathew 5:45 where God says, “That you may be children of your Father in heaven. He causes his sun to rise on the evil and the good, and sends rain on the righteous and the unrighteous.”
I never seen anything like this before in my life. MS is the lonest, the most expensive, the most complicated and I can go on forever. I never experienced anything like this before. Right now, I feel like I'm the only person in the world. I feel like nobody cares and if they do, well, they don't understand. With MS, to not understand or to not care is the same thing. Because with both, one can not relate to the MS patient. Speaking personally, that is what anyone with a chronic disease need, someone to understand and have the ability to relate to the disease and all the obstacles that come with it. I think I'm overwhelmed. Sometimes I think too much. However I saw a quote that said "Sun is alone too, but still shines." That made me smile and remember that God said, “In the same way, let your light shine before others, that they may see your good deeds and glorify your Father in heaven.” Matthew 5:16 Even though some don't understand or whatever t...
I was talking to my niece today & she asked me, what did I have plan for today? I had to explain to her that with being diagnosed with MS, my days are based on how I feel. If I don’t feel it, I don’t do it. The only thing that I do even when I don’t feel up to it is, get the Tysabri treatment. (Read more @ Tysabrihcp.com ) . This medication does not change the way I feel. It does what it is designed to do and that is slow down the progression of the disease. Once I understood that, I could deal with getting it better. On most days I feel fatigue, pain, pens & needles feeling in my feet. The pain is never in the same place. It could be in hands, feet, legs, back, head, eyes, face or whatever MS decides to do on that day. I like to use the terms that MS is sneaky and unpredictable. I never know what I’m dealing with. In not knowing what I’m dealing with concerning this disease; however I do know who kn...
Comments
Post a Comment