Hep C Post tx long term sides 2003

I am  not sure have this, but I everyone of the symptoms. I was 1A genotype and went through  8 months of Peg-Intron
and obtained a SVR in 2003. Treatment almost killed me. I had a heart murmur that got worse and I had horrible side effects including ever since.

I have mobility problems of the esophagus, severe GERD, memory loss and loss of my motor skills, both gross and minor. I now have lots of balance and coordination problems. Normal MRI. I fall all the time now and I am a disaster in the kitchen. I always spill, drop things and trip over my own feet.I had neurological defiects for about a month before I quit treatment.

Loss of memory, especially sort term. I can't write or spell anymore. I don't know what to do. No one believes that I got these problems from the Peg-Intron. I KNOW THEY ARE WRONG!!

I now  have chronic fatigue, deprssion,anxiety, agoraphobia and social withdraw. I also have mild overall edema that no one can explain. I feel much worse now than I did before tretment,lol.

My life ***** now! My son asked me if I was sorry I went through the treatment, and honestly I couldn't give him an honest answer. I only wish someone had told me the possible long term effects, so I could have made an honest decision" treat" or "not to to treat" My became hypothroid in the first 8 weeks.

I don't know if I have this, but I do have many of the symptoms.
I became permantey disabled after the treatment.

I used to be a high risk ultrasound tech.I am unable to work now.

[Heiferly]

Which form of dysautonomia do you feel you have the symptoms of?  

Do you have orthostatic symptoms (symptoms that appear or worsen upon standing but resolve or improve upon lying down)?  How is your blood pressure?  Heart rate?  Do you know if they change significantly between lying down or sitting and standing?