Atsugi
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  • Its RHC4 not GM06...Yes i know its not good for my mental health but what can i do...when i have a non stop 24x7 twitching in my calves and feet...it can not make me calm...its now five months i am passing with this muscle twitch,,,Now dr told me for an emg, i know something is going wrong... :(
    Mr Mike don't angry please.I know you do not like me but please see it..i think there is hope..http://www.als-new-drug.com/
    Visit this site,,a new drug. They r giving it free...here a member of this forum also used it for nine months and he has some improvement ....
    Do u know about GM6? MAY BE IT WAS APPLIED 12 ALS patient...and there were some success.i read it from ny times
    Mr Mike,
    I do not know how to send you inbox message..in the repprt i saw 24 to 190 cpk is normal,i have 140..but is it considered as high as my age 30? Ncs and emg ate not same? In many website write ncs/emg as same function for nerve condition test..sorry for my bad emglish.
    Hi,I have visited neru with his prescribed test,,my ths t4 and diabetics normal,s.cbk also 140IU/L,,after shpwing these he told me to do mri spine and ncs and he said me to get admitted in hospital:(...is 140 cpk high?
    Hi Mike, I was hoping you would be able to answer, I know my symptoms say they point away from als, but can you answer would bulbar onset present as weekness in my finger, for the past couple of days my finger feels different like I don't have the same use when I type, just hoping for a little insight here, you have been so helpful
    Hey mike sorry if I offended anyone it wasn't my intent I apologize. I just have a lot of the same symptoms as a pal here and he has the respiratory onset like the progressive shortness of breath and tight ribcage stomach and back cramps I fear this may be it mate
    This was the message that I posted but didnt see a reply...Hey Mike, have not heard a reply back I am so confused when we post about symptoms and we very one says they don't match up to ALS yet I read other posts and see Peopl diagnosed with excess saliva or body wide twitching and swallowing issues I just don't know what to think or say when people say does not point to ALS yet other sites do, I guess i am just confused and super scarred
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