denise5700
Greenlighter
- Joined
- Aug 8, 2017
- Messages
- 1
Hello. I am new today and I just need to find an outlet for everything that is going on in my life. First off, I have very high anxiety which is being exacerbated by things that are happening lately. Within the last few years I have resigned from 2 jobs because of extreme bullying. I seem to encounter very abusive people everywhere I go and they make my life very difficult. I am very friendly, perhaps a little too trusting of people and a little sheltered. I am not a wordly type person who can express herself well I tend to be a little on the Asperger's side and over the years have learned skills so I can be more sociable and blend in etc. I do prefer to be quiet, alone most of the time but do like to company, however I do not have anyone to get together with at this stage in my life, just a few groups from church etc. I have had learning disabilities all my life and do not retain things very well that I learn. I have few interests and it is very hard for me to travel or pack, organize, plan things due to sensory processing issues (long term in my life). I suffer from fibromyalgia also.
I recently was referred to a neurologist for a MRI of the brain. I was concerned about MS but I do not have it according to several doctors. However, fast forward 3 years I am having a few balance issues. Nothing too serious but it started with tottering but it has progressed along with some spatial issues. If I put my hand out to pick something up there seems to be unwanted movements. It is not a smooth and fluid action like it used to be. I have always been unsteady on step ladders and avoided them. I feel the balance issue started a long time ago. I saw signs of it but it became more pronounced 3 1/2 years ago. I went to the doctor again and she referred me for neuropsychological testing which is next week. However, a new neurologist who I had never seen agreed with the MRI and said he didn't think I had MS but he said I had bilateral parietal atrophy and the MRI was repeated last month. The results are the same and he said it hasn't progressed. I went for an EEG and it was negative. I was referred to a neurologist for balance issues and he specializes in movement disorders. He said, if anything, it was very subtle. Of course, I didn't do much of it in the exam room so I had to demonstrate all the things which have been happening lately. I took a brief RX for Buspar and noticed some of these symptoms and discontinued it, however I forgot to mention this to him as there has been so much going on. I also have borderline low iron from an hematocrit and took an iron supplement and it is okay now. Low iron can cause you to have a staggering gait which I have had.
Well, I do research on line and find out that bilateral parietal atrophy is associated with early onset Alzheimer's and it will spread into the frontal regions of the brain. I was absolutely shocked. The neurologist didn't mention this to me and I know I have to do the neuro testing first before they can diagnose anything. When I saw the movements disorder neurologist I mentioned this and he confirmed it. He hasn't diagnosed me yet either but said in his notes that it is in the parimeters of early onset Alzheimer's, PCA or corticobasal syndrome. I just remembered last week that I had a MRI about 15 years ago for a worker's comp case where the neurologist told me that it was fine but my brain was small but not to worry because it doesn't affect intelligence. He didn't elaborate and I didn't know to ask back then about focal or generalized atrophy.
Since I have had these problems all my life with comprehensive, learning disabilities, low executive skills etc. my question is perhaps the parietal lobes didn't develop fully from childhood? I am almost positive that this is the case. I really do not think I have Alzheimer's because I am not experiencing any memory problems. My frontaltemporal lobes are fine, tightly packed they said. I am absolutely terrified. I can think of nothing else. I am having nightmares. I am having flashbacks from these horrible jobs where these women bullied me and practically could have had me fired for nothing but I managed to resign just in time. I am very detail oriented, conscientious and dependable. I feel I threaten people, if anything. My job performance absolutely had nothing to do with my symptoms. I work part time. I know I have to wait until the testing has been done. I feel confident it will be okay but then does it account for learning disabilities? I have never been able to draw very well. The three dimensional boxes and moving lines around to make shapes is impossible for me. I could never do it along with other things. But, other things I do fine with. I am so scared. I am not working right now so that gives me more time to worry? Is it possible to have undeveloped parietal lobes? I did ask if perhaps they could not have fully developed. They weren't sure but said it looked like atrophy. I am 57 years old, with the first current MRI done in 2014 - no changes, which is good. So, can anyone give me any information that perhaps will calm me down? Thank you very much for reading my post.
I recently was referred to a neurologist for a MRI of the brain. I was concerned about MS but I do not have it according to several doctors. However, fast forward 3 years I am having a few balance issues. Nothing too serious but it started with tottering but it has progressed along with some spatial issues. If I put my hand out to pick something up there seems to be unwanted movements. It is not a smooth and fluid action like it used to be. I have always been unsteady on step ladders and avoided them. I feel the balance issue started a long time ago. I saw signs of it but it became more pronounced 3 1/2 years ago. I went to the doctor again and she referred me for neuropsychological testing which is next week. However, a new neurologist who I had never seen agreed with the MRI and said he didn't think I had MS but he said I had bilateral parietal atrophy and the MRI was repeated last month. The results are the same and he said it hasn't progressed. I went for an EEG and it was negative. I was referred to a neurologist for balance issues and he specializes in movement disorders. He said, if anything, it was very subtle. Of course, I didn't do much of it in the exam room so I had to demonstrate all the things which have been happening lately. I took a brief RX for Buspar and noticed some of these symptoms and discontinued it, however I forgot to mention this to him as there has been so much going on. I also have borderline low iron from an hematocrit and took an iron supplement and it is okay now. Low iron can cause you to have a staggering gait which I have had.
Well, I do research on line and find out that bilateral parietal atrophy is associated with early onset Alzheimer's and it will spread into the frontal regions of the brain. I was absolutely shocked. The neurologist didn't mention this to me and I know I have to do the neuro testing first before they can diagnose anything. When I saw the movements disorder neurologist I mentioned this and he confirmed it. He hasn't diagnosed me yet either but said in his notes that it is in the parimeters of early onset Alzheimer's, PCA or corticobasal syndrome. I just remembered last week that I had a MRI about 15 years ago for a worker's comp case where the neurologist told me that it was fine but my brain was small but not to worry because it doesn't affect intelligence. He didn't elaborate and I didn't know to ask back then about focal or generalized atrophy.
Since I have had these problems all my life with comprehensive, learning disabilities, low executive skills etc. my question is perhaps the parietal lobes didn't develop fully from childhood? I am almost positive that this is the case. I really do not think I have Alzheimer's because I am not experiencing any memory problems. My frontaltemporal lobes are fine, tightly packed they said. I am absolutely terrified. I can think of nothing else. I am having nightmares. I am having flashbacks from these horrible jobs where these women bullied me and practically could have had me fired for nothing but I managed to resign just in time. I am very detail oriented, conscientious and dependable. I feel I threaten people, if anything. My job performance absolutely had nothing to do with my symptoms. I work part time. I know I have to wait until the testing has been done. I feel confident it will be okay but then does it account for learning disabilities? I have never been able to draw very well. The three dimensional boxes and moving lines around to make shapes is impossible for me. I could never do it along with other things. But, other things I do fine with. I am so scared. I am not working right now so that gives me more time to worry? Is it possible to have undeveloped parietal lobes? I did ask if perhaps they could not have fully developed. They weren't sure but said it looked like atrophy. I am 57 years old, with the first current MRI done in 2014 - no changes, which is good. So, can anyone give me any information that perhaps will calm me down? Thank you very much for reading my post.

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