Let me preface my twitching onset: I'm a 26 year old male. I had never really had health anxiety until I had a doctor tell me I may have testicular cancer early this year in January. It really put me into a full on panic mode. I was cleared of having cancer, but literally the day of the Ultrasound I began having chest pains which set me into a whole new state of panic. I went to one of my GPs (i have one I can just pop into without an appointment) and was complaining of chest pains and it felt like I could not get a full breath. They gave me a shoddy lung capacity test and told me my lungs were only outputting about 60% of air lol, so that put me into even more panic for another month. Went to a pulmonologist and found out my lungs were perfectly normal. So all in all I had about 5 months of unnecessary health anxiety which prompted my twitches. I was told I had likely developed GERD from all of this and was put on Omeprazole which seemed to curb the chest pain.So, I started twitching initially on my right ear in April, then it moved to one arm and then the other and by May I had widespread twitching. So I've been full blown twitching for about 5+ months: all over my face, head, arms, legs, arches of feet, stomach, chest, back, etc etc. Initially I was having hand pain that accompanied all of this, mainly pain in the finger tips which would get insanely painful after lifting or moving anything. I went to a GP 2 months ago for the twitching and was told I had very low vitamin D levels, so I've been taking vitamin D. He didn't refer me to a neuro or try to perform any strength tests (guessing the thought of ALS wouldn't have even entered his mind and really didn't enter mine either at the time). I also have this thing going on where my muscle movement is very unsmooth. If I sit in a chair and left my heel off the ground then try to return it to the floor, my ankles/legs shake uncontrollably as they go back to the floor. I get a similar thing with my flexing/deflexing of biceps though it is not nearly as prominent. My neck muscles do something similar. I posted a video of that in a BFS Questions thread.A month ago I started reading this website and it prompted me to look at my tongue. I noticed my tongue is pretty much twitching all the time and that I can't feel any of those twitches. Either I can't fully rest it or they're real twitches. Even with that information, I was still sort of "over" my twitching and I wasn't really very concerned anymore. However, a few weeks ago I started having to clear my throat daily and that sort of set me into full on fear mode of Bulbar ALS
. I feel like I constantly have to clear my throat/cough so I can speak correctly. Now, just this last week my tongue has begun to fissure along with the twitching. I had one crack open up (half an inch long) a few days ago and now I have a second starting right by it. I'm not sure if a cracking tongue is a bulbar ALS symptom but it is sort of scaring me that it is some sort of muscle loss/atrophy. I can still do everything I can think of and speak normally and swallow normally as far as I can tell (though I've stuttered my entire life so it is not like someone would tell me if I sounded funny
). If I rest my tongue in my mouth as much as I can, I get rapid twitches on the surface of the tongue. If I stick my tongue out or put it to use in any way then my tongue looks like a box of worms. Fully stretching my tongue actually reduces the twitches since It is likely more difficult to see anything and the muscle is being fully used.I made a short video even though I know no one here can really tell me anything about my tongue twitching. I guess it just helps to get stuff in the open. I'm finally make a neuro appointment tomorrow as I've been putting it off for over a month and just need to get it done.Video is basically: Tongue at rest, tongue slightly extended, tongue showing fissure. Sorry for the poor lighting and video quality
. For whatever reason, I can't find a render quality that is as good as how I took the video, so the twitches are a bit more blurry/harder to see. It is also a bit harder to rest my tongue and shoot the video, but the surface of the tongue looks about the same either way.Tongue video formats:WMV - MP4 - Thanks for any thoughts.


