Well i am new here not really i have been following the board since February and it has helped me learn a lot. I am Asian (not many I notice here who cares) and I work as a web designer. I am on the over weight side but I am pretty sporty as I play tennis a lot. Unfortunately during winter in Canada I dont get to exercise much and I gained more weight and one day I realised while holding the fork my left finger would tremble it did freak me out and I work with computers a lot and noticed that too when I was using short cut keys when I press down my left fingers would shake. It was scary and then I fell sick with severe gas that would cause palpitation especially if I was lying down on the bed I mean it felt like I was going to have a heart attack at times. Anyway I went and did a blood work they found that my Hpylori level was pretty high in 68. I also had a mild CPK level of 212 which i had no idea what it was and doctor did not bother about it much. So he put me on the HP Pac One of the worst medication I ever took and think if I ever get Hpylor again I will never take this medication. I had to take Moring and Night 4 tablets. When I took the first dosage I still went to play tennis that day cause I did not really feel any weakness or anything from the medication.But the next day my right hand fingers were stiff with pins and needle and it hurt a lot. i had to squeeze my fingers or put in hot water to get relief. it was so scary I broke down almost.I could not even tell whether this was the medication or i might have injured myself from playing tennis but I still continued the medication. I had strange shakes on my body even lying down my head would shake or if I am sitting lets say like people meditate position my back would move up and down automatically!!. This things freaked me out. My hand stiffness would come and go and somedays nothing at all. Then of of course by end of Jan this year came the worst. I was going to sleep and my body was jerking every time I would fall asleep as they call it restless leg and from there full blown twitches all over my body calf arms shoulder and tingling sensation on my feet like electric current a lot. And yes Mr Google put my anxiety off the roof with ALS thing and it wasnt really the twitches part that freaked me out it was the hand part more
And also the last retarded symptoms I got was sweaty feet which I never in my life had. My hands are dry always.Coming to this site did relax me a whole lot as for for my condition now. I dont have the shakes when I lie down and my twitches are not like thousand like some of you have they few here and there much less than what it was. I uped my Vitamin B12, Magnesium and Vitamin D. The B12 helped me with the shakiness when i used short cuts on the computer.But I dont think my hands are getting better cause now if I play tennis I realised my fingers hurts a lot after the game even at night time I have to use heated mediction cream on my hand and wrap it my cloth so I can sleep if not it just hurts badly. And the worst is when I am around people especially difficult clients who can give me a hard time I feel my fingers hurts like hell and at times my legs feel wobbly also.And yes whatever this is is winning me over with severe depression, the people I love the most are being hurt as I push them away, I am going to be 29 in 11 days. I am a very simple boring person, I dont smoke or drink and its very hard to talk to someone about my symptoms cause they just dont get it. Sorry for the long boring post and wish everyone a healthy week ahead. TonyPeople can spend 8 billion dollars on a garbage to find out how the universe was created but cant look into this type of serious deadly condition.
