i just wanted to add, ive been extremely moody im not myself at all, im 44 yrs old male have two children and wife, when i try to explain to the doctor whats going on with me
all they want to do is cover up with the drugs, ive been threw alot of changes the past ten years, im currently on lunesta because of sleeping problems, now i cant go to sleep without them " just xxxxwonderful " somtimes the concern really gets to me
i find myself going in the bathroom crying myself calm, i wish doctors wouldnt push
drugs on people and get to the real problem. just my thoughts on it
would love to hear feedback
the past year ive been having continuous mucle cramping, sometimes in both feet at the same time
in both triceps same time, my left tricep constantly tightening as if i were flexing. any specs will help
I have the same early symptoms of my brother. I have had to EMG"S in the last year. The first Neuro. dx me with BFS nad Peripheral Neuropathy. The scind specialist I went to in july, saw the twitches with his on eyes. He said I needed a Thyroid, Magnesium, Calcium test. I had my GP do the test.she even added the Lyme test. They all came back normal. As did Timothy's. So I don't know from here. I am not going back until something drastic changes. I am on meds for th Twitching and Cramping. Zanaflex and Clonzepam and Loratab when needed. I awoke during the night last night with severe spasams and cramping in my left foot and calf. A normal thing lately. And cramping in mu upper arms.
I hope you get yours under control. Nerves will cause a lot of strange things.
Good Luck!
Lorie
No cramps. Just the twitch, anxiety is a factor I am just hoping it's not a bi-product. Did you say you had the same symptoms as your brother or as me? Have you had an EMG?
I have no doubt this disease is caused by environmental toxicity and it's also affects us through out diet.
My brother Timothy has ALS. I also started having the same symptoms 1-1/2 years ago. No dx for me. Timothy had symptoms for 7 years before the Neuro's. suspected ALS. 2-/2 years dx.
I can tell you with Tim's experience and other ALS patients I know. there is no specific time line for any one person to be dx. Try to stay calm, nerves only make it worse. I could be BFS or Nerves or something minor. The bright side is you don't have Atrophy. Are you having Muscle Cramps?
Here to help,
Lorie