hmj82
Member
- Joined
- Jul 9, 2015
- Messages
- 13
- Reason
- Learn about ALS
- Diagnosis
- 00/0000
- Country
- US
- State
- PA
- City
- Pittsburgh
Hello,
First off I just want say how courageous all of you are who have been diagnosed with this terrifying disease. I truly appreciate your feedback on my symptoms.
I'm a 33 year old male. My symptoms started off at the beginning of June with weird head pains/sensations. It felt almost like zaps that would occur for a second and then move to another spot in my head. It wasn't extremely painful more annoying but I've never felt them before in my life so after I couple of days I went to my PCP. My PCP thought it was just a migraine so he told me to relax drink water and take Aleve. After a week of not feeling better I saw him again which at that point he scheduled a brain MRI. I got the results a week later that there was no sign of cancer or tumor but there was some spotting noted so he referred me to a neurologist. During the past couple of weeks, I've had muscle twitches in every part of my body just about and also had intermittant migratory pain which almost felt like nerve or bone pain. I've seen the neurologist twice now and done NCV's on my arms and legs and an EEG which were normal and gotten bloodwork (CBC, ANA, SED rate, Lyme, Vit. D, THY, and Metabollic) which were all normal. Over the past week, I've developed really bad dry mouth and difficulty and painful swallowing. My neuro has told me that she thinks it's just stress and anxiety. Does this sound like ALS? I've read the stickies and some of it sounds like it and some of it doesn't. I just wanted your opinion.
Like I said above, I really admire everyone who is struggling with ALS so please don't take offense to my post I'm just really worried at this point as I haven't felt much progress in 5 weeks.
First off I just want say how courageous all of you are who have been diagnosed with this terrifying disease. I truly appreciate your feedback on my symptoms.
I'm a 33 year old male. My symptoms started off at the beginning of June with weird head pains/sensations. It felt almost like zaps that would occur for a second and then move to another spot in my head. It wasn't extremely painful more annoying but I've never felt them before in my life so after I couple of days I went to my PCP. My PCP thought it was just a migraine so he told me to relax drink water and take Aleve. After a week of not feeling better I saw him again which at that point he scheduled a brain MRI. I got the results a week later that there was no sign of cancer or tumor but there was some spotting noted so he referred me to a neurologist. During the past couple of weeks, I've had muscle twitches in every part of my body just about and also had intermittant migratory pain which almost felt like nerve or bone pain. I've seen the neurologist twice now and done NCV's on my arms and legs and an EEG which were normal and gotten bloodwork (CBC, ANA, SED rate, Lyme, Vit. D, THY, and Metabollic) which were all normal. Over the past week, I've developed really bad dry mouth and difficulty and painful swallowing. My neuro has told me that she thinks it's just stress and anxiety. Does this sound like ALS? I've read the stickies and some of it sounds like it and some of it doesn't. I just wanted your opinion.
Like I said above, I really admire everyone who is struggling with ALS so please don't take offense to my post I'm just really worried at this point as I haven't felt much progress in 5 weeks.