On 28 Mar 2007 19:11:04 -0700, "jelato" <jelato@gmail.com>, in message
ID <1175134264.909067.179750@y66g2000hsf.googlegroups.com>, in the
newsgroup alt.support.hepatitis-c wrote:
>Hi, I have a friend who has been in hep-c treatment for the most of 3
>years. For all this time his medicine has been about the same. I dont
[quoted text clipped - 10 lines]
>area if you know doctors here. Do you all have any advice? Thanks so
>much.
Sounds like something is wrong if on tx for three years. I have heard
of someone who found the virus hard to shift doing two years but that
is very unusual. Although I only know what I read on here about
Infergen, I don't think I've heard of anyone doing more than one shot
per day - though others may know different.
The bit that concerns me is the apparent obstruction to getting a
second opinion. Any decent doctor should welcome that.
Rages and not keeping it together is not at all unusual with treatment
though. The side effects can be pretty crappy. Sometimes an anti
depressant can help though I never went down that route myself.
Some doctors are pretty awkward with keeping patients informed but
will co-operate with another doctor. Could it be a procedural problem
with the second opinion? Maybe the second doctor has to be seen so
that he/she can request the patient's notes?
dBo - 29 Mar 2007 21:16 GMT
I stayed very proactive from the moment I was diagnosed. My doctor had
no problem whatsoever with sending me copies of all my bloodwork, lab
reports, xrays or anything else I wanted. I was having blood work done
every two weeks due to severe anemia etc and if I didn't have any
given results in writing within a week, I just dropped by and asked
the secretary to print me up a copy for my records. (I'm in New
England area) I educated myself and when we met, I was able to discuss
my questions intellegently, and he was clear right up front that I was
"doing my homework", and he was patient while I made him repeat
everything 10 times, and wrote it down,because after all, my brain had
sh.t the bed, on treatment....
. It was important to me to carry copies of all this stuff with me
everywhere - in the event I became ill, or was in an accident or
something I wanted all that information on my person! Personally, if
my doctor had refuse to give me my own records I'd have found another
doctor rel quick, but that may just be ME.
greyhackles - 29 Mar 2007 23:59 GMT
>I stayed very proactive from the moment I was diagnosed. My doctor had
>no problem whatsoever with sending me copies of all my bloodwork, lab
[quoted text clipped - 13 lines]
>my doctor had refuse to give me my own records I'd have found another
>doctor rel quick, but that may just be ME.
You sound like you could be my long lost brother :-)
Aside from me actually doing weekly blood tests for the last 37 weeks of my
therapy, you could have written my medical diary while on therapy.
If you wanna see something really OC on the topic, check this out:
http://home.comcast.net/~greyhackle/therapy.htm
Be sure to click on the Chart buttons at the bottom :-)
btw, the "liver pain" the last few months turned out to be a bit of
diverticulitis in my ascending colon. Lousy coincidence as it had me at wits
end at the time...
Cheers
/greyhackles
jelato - 30 Mar 2007 01:40 GMT
> >I stayed very proactive from the moment I was diagnosed. My doctor had
> >no problem whatsoever with sending me copies of all my bloodwork, lab
[quoted text clipped - 34 lines]
>
> - Show quoted text -
Hi thanks to everyone for your advice. I will talk to him tonight to
see what his dose of intergen is and how many times a day he takes
it. The anti-depressants didnt seem to help, but he uses Lyrica for
nerve pain, and he says it is wonderful for his depression. Go
figure.
Jack Black - 30 Mar 2007 10:12 GMT
The attached link seems to be advocating at least 12 months treatment for
geno 1. This is new to me. I'm 1A and I'm just finishing a 48 week
treatment. Is this current practice now? Damned if I'm going to do another
month at this point.
Jack
>>I stayed very proactive from the moment I was diagnosed. My doctor had
>>no problem whatsoever with sending me copies of all my bloodwork, lab
[quoted text clipped - 34 lines]
>
> /greyhackles
greyhackles - 30 Mar 2007 15:03 GMT
>The attached link seems to be advocating at least 12 months treatment for
>geno 1. This is new to me. I'm 1A and I'm just finishing a 48 week
>treatment. Is this current practice now? Damned if I'm going to do another
>month at this point.
>
>Jack
48 weeks is the standard for g1s. Some folks can't help but round that up to
"a year" when discussing it, but it's still 48 weeks.
You're a done dood ;-)
Cheers
/greyhackles
Tell him to DEMAND a copy of his records, and run--don't walk--to another
doctor. If what you're saying is accurate, the whole things smells really
bad.
> Hi, I have a friend who has been in hep-c treatment for the most of 3
> years. For all this time his medicine has been about the same. I dont
[quoted text clipped - 10 lines]
> area if you know doctors here. Do you all have any advice? Thanks so
> much.