Father's Courageous Battle with ALS

[Tulio]

thanner - I read a few of your posts in the past and have to say you are taking this amazingly well considering your father was disgnosed with MSD (ALS). I also read his website and he's got a great deal of courage.

Did you get referred to a Neuro by your GP? Mine didn't even want to hear about it even though I visited her about 4-5 times in the last 4 months. Then I did some of my own research and took ALL of my symptoms into consideration and figured it could be yeast. So I'm giving it a go, and as I said some of the symptoms have already cleared and the twitches are about 50% less of what they were.

Anyway, I hope the weather in New Plymouth is better. I live in Wellington and summer is only just starting to arrive here (with the wind).

 

[olfjohnsmithgolf]

i know what you mean . i think at first we all worry but after seeing doctors, having test after test, spending money we just get tired of worrying and realize that its nothing to worry about just a screwed thing we have to deal with. hey at least its not ALS, cancer, parkinsons,MS, dibetes, tumor,blindness,etc etc i could be alot WORSE right. its just tough dealing with it at first our minds take over and anxiety kicks in. we are looking for answers to make it stop stop RIGTH now and thats not happening. the drugs they want to pump into you just make things worse. we need to find peace of mind and thats not easy but we must keep trying. i agree the internet hasnt helped me i think it made thigs worse. i spend to much time trying to self diagnose with no avail. oh weel time will tell. god bless all