I am new to these boards. I am a 55 year-old male and I have been advised by my doctor that I may have ALS. The main symptom, of course, is muscular weakness, which has progressed very rapidly during the last 2 months. I lift weights and I estimate I have lost about 5% strength during that time. In addition, I have lost about 30% strength on my right arm. Since I lift weights, I keep an account of the amount of weight I lift as well as the number of repetitions I perform.
Last month, I had complained to my family doctor about strange sensations on the top of my head. While my head did not hurt, the right side of my scalp felt tender even though I had not injured myself. He suggested an MRI. The MRI came back with some "spots," which he described as common and that they might not mean anything. His diagnosis at that time was neuralgia. However, he also mentioned MS as a possibility. This last time when I informed him of my general and asymmetrical loss of strength, he also mentioned ALS. I have been referred to a neurologist, so I have to play the waiting game. I have no other sensory changes that would indicate MS. Although I know that fasciculations without loss of strength can mean anything, I have suffered from such twitches for years. Perhaps, the loss of stength has been gradual over time, but I was not able to measure it until now. Since I have no other explanations for the loss of strength, I fear the worst. Thank you for reading this and please let me know what I should look for during the neurological exam or the type of questions I need to ask. I live in a small town, so I will not be seeing an ALS specialist.
Last month, I had complained to my family doctor about strange sensations on the top of my head. While my head did not hurt, the right side of my scalp felt tender even though I had not injured myself. He suggested an MRI. The MRI came back with some "spots," which he described as common and that they might not mean anything. His diagnosis at that time was neuralgia. However, he also mentioned MS as a possibility. This last time when I informed him of my general and asymmetrical loss of strength, he also mentioned ALS. I have been referred to a neurologist, so I have to play the waiting game. I have no other sensory changes that would indicate MS. Although I know that fasciculations without loss of strength can mean anything, I have suffered from such twitches for years. Perhaps, the loss of stength has been gradual over time, but I was not able to measure it until now. Since I have no other explanations for the loss of strength, I fear the worst. Thank you for reading this and please let me know what I should look for during the neurological exam or the type of questions I need to ask. I live in a small town, so I will not be seeing an ALS specialist.