I read your 2008 post and your story was very much like mine. Pain the moves around, fairly sudden onset. May I ask how you are doing? Were you ever diagnosed?
Hello mam, I have posted a thread yesterday, Suspecting misdiagnosis after 10 years, but haven't received any comment. I really need to know the experience of people whether I am misdiagnosed or not ? I am new to alsforums & don't know how to spread my thread to other members. please help me to get comments from experience members. Thread link: http://www.alsforums.com/forum/do-i-have-als-als/20125-suspecting-misdiagnosis-after-10-years.html
I saw you are located in Oakland Co., MI. I am in Sterling Heights, (Macomb Co.)
I struggled with a possible ALS diagnosis for over a year and then possible MS for 6 months. I have both upper motor neuron signs like spasticity and an abnormal babinski reflex and also lower motor neuron symptoms like weakness, fasciculations, and atrophy.
I can no longer walk unaided and have lost the use of my left arm and hand. (I am typing this with one hand).
I finally became my own doctor and found a Lyme Doctor in Michigan. I had my blood drawn and sent it to IGENEX.
In June 2011, I tested positive for lyme and began oral antibiotics. I have received no results and am scheduled to receive a PICC line tomorrow. I will be receiving the antibiotic Rocephin.
hey sweet lady,were have you been hiding?
saw you dropped in on me.........but no message!
hope you are doing ok and your beautiful family.
dont be such a stranger...........take good care.caroline