Dealing with this brain tumor has been very taxing the last couple of months. It started with frequent headaches accompanied by black spots in my vision. This absolutely freaked me out and I was at my doctor’s office within the week, he then referred me to a neurologist who ordered a CT scan for me. The tumor is the size of a Penney and I now have to see an oncologist. They have ordered me to have chemotherapy as well as radiation. The chemotherapy makes me sick and nauseas but the medical marijuana that the Doctor prescribed has helped with my appetite. I have been lucky enough to keep my hair although it is thinner unfortunately my eyebrows are gone and I now have to draw them in. I’m very blessed with an employer that is understanding and
I will be talking about a time in my life that was not easy that i had to go through. When I was around age 5 my mom noticed a lot of twitching and blinking of my eyes she was worried and had no idea what it was, so she took me to the doctor. They said I had focal seizures, as a little kid you don’t really understand or know how to feel. But I could just remember my mom constantly worried about me. The reason behind me having these seizures, was when I was born there was a part on my lower brain that didn’t form so it left scar tissue and was causing them. But at the time we were still living in Texas the doctors tried multiple surgeries, but none of them helped so we moved to Tennessee for better doctoring. That’s when I started going to Vanderbilt and ever since then it’s been a journey.
My neurosurgeon, husband, daughter, and I agreed to a plan. On February 18, he will be removing the right side of my hardware from my skull down to C-2/3 where he will saw the rod in half and leave the rest of my fusion. The right side of my fusion has failed. While removing the fusion, he will be taking four screws out of my brain and one out of my neck. My fusion was placed nine years and two months ago; therefore, it has been in my body for a long time. He is leaving in the left side of my fusion, which is from my skull to C-5 because my neck is not stable enough without it. After he removes the titanium hardware, he will be taking a cadaver bone as well as removing bone marrow from my hip to rebuild my skull. He has to cut down the
Over the past four years, I have seen more doctors than an average person will see in a lifetime. From endocrinologists to neurologist, I have tirelessly sought medical treatment for multiple brain injuries I incurred at a young age. Through my personal struggle, I learned that there is limited treatment for concussions and traumatic brain injuries in the state of New Mexico. It has become apparent that there is a lack of treatment not only for brain related issues, but for all health issues in the state of New Mexico, especially in rural communities such as mine.
Hi! My is Ginger and I am 40 something (lol). I am married and have 4 children and 2 granddaughter & expecting another grand daughter in Oct. I am currently in grad school and I have just been diagnosed with ADD. How in the world can someone in their 4o's just find out they have adult ADD?
Recently I discovered that I have brain tumor. My surgery is scheduled in two weeks, unfortunately this requires an incision in my frontal lobe. This will cause loss of intelligence, personality, and behavior. I have Fourteen days left with a fully functioning brain, wanting to spend this time doing what I love made me decide what to do. In this two week period I will focus on family, friends, and some of my favorite activities. The first five days are going to be spent with my family at Smith Mountain Lake. Following the time at the lake I will rent a beach house and pack it full of my longtime friends. Lastly in the final days leading up to my surgery I will be in the mountains doing what I personally enjoy most. Overall I will be relaxing,
Over the past four years I have seen more doctors than an average person would see in their lifetime. From endocrinologists to neurosurgeons, I have tirelessly sought medical help to overcome multiple traumatic brain injuries I incurred as an early teen. Prior to these head injuries I wasn't exactly sure what I wanted to do with my life or what my future would encompass. The outlook I had on life prior to my head injuries has drastically changed through the course of my recovery. Although my road to recovery has been filled with hardships, disappointments, and pain, I have found a new direction filled with opportunity to advocate on behalf of others.
I don't know where to start. I'm 25, male, and I live in southern state. I suffer from epilepsy, depersonalization, depression, and hypothyroidism. I don't know what to do anymore...
Being a child with ADD I found school to be very challenging even at an early age. My first year of high school was a big leap from elementary and middle school. It was very hard for me to get use to the tests and work that were given to me. During that time I wasn’t sure what I wanted to do and that made it very difficult for me to really want to do well in school. Once freshmen year past I went on a trip to Europe which changed everything for me after that I knew I wanted to do something with international travel. I heard about a family friend who was involved in international business and how he got to travel everywhere and at that moment he was living in Brazil. To me that was everything and I had found my goal. I started to do better
It’s a struggle to get out of bed sometimes, I often just sit there struggling to comprehend the sequence of events which have taken place over the past year. I mean, I’m used to this now, its normal to me, but the fact that this has happened and that I am now ‘disabled’ as people would put it is hard to get my head around. And every time I look down I’m reminded of the pain and the struggle I faced, it’s a physical scar which links me to my grueling past, a physical and emotional journey.
I woke up to the sound of sirens, getting louder and louder each second. A state of panic filled my neighborhood. My heart dropped to my stomach as I watched my neighbor get strapped onto a stretcher and rushed out of the neighborhood to the nearest hospital. As I sat there, holding my neighbor’s two young boys in my arms, I realized that those sirens had awakened me and opened my eyes to a world that a child could not understand. In this single moment, I was maturing and preparing myself for adult-like responsibilities.
If I were a psychoanalyst treating disorders, I would deal with the behavioral aspect of the disorder. With the behavioral point of view, it involves a multitude of developments such as phobias, anxiety, and other various situations. I personally like the behavioral aspect the most because it starts by taking on a certain person’s fear with the same ways it was originally developed. For instance, say somebody has a social phobia and cannot handle being in certain places due to a large amount of people, this individual may love sports but will not go to events due to high volumes of people which results to watching all games on TV. I would simply start to figure out why this all began, then slowly bring in different solutions. One way could
An auditory processing disorder, is when your ears and brain don’t cooperate together, the ways in which the brain interprets sound through speaking and or sounds.
I loved your post. I completely do this all the time and I hoped your dinner turned out awesome. I do think didn’t think it was as humorous, some steps you could have taken to help with your preoccupation is responding, and being mindful of your coworker. You were off to the right start by asking her questions but I think you should have responded to her and it would have helped your mind not to wander. “Mindfulness is being fully present in the moment” (Wood, 2016). Even though you were hungry and dinner sounded wonderful, I don’t think you were fully present in the conversation. Great post.
The biggest obstacle that I have encountered in my ability to read and write are my learning disabilities. I’ve went through 18 years of my life before they were identified, and they have caused me so much frustration. I couldn’t understand why other kids could read out loud so well and I couldn’t. I couldn’t understand why it took me so long to read only a few pages of a book when other kids were at the end of the chapter. I had no idea why I couldn’t even sit down to write a single paper when other kids were doing their essays in a span of a couple hours.