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When I decided to do tx, my wife and I both agreed that if the sides were too hard, I would quit. So, if you decide to quit, so be it. It's your decision. But, if there is anything I can say that would encourage you to keep on, let me say it. You are 27/48, meaning there are more behind you than in front of you. I assume since your dr has you going, that you cleared (or log 2 dropped) at 12 weeks, so the stuff is working. Think of the sides as the dragon putting up the fight of its life because you are out to kill it. Hang in there, Dallas.
My sides got worse in the last couple of weeks, too. Perhaps you have a virus or flu on top of it. My PA thinks that's what happened to me. "Just because you're in treatment doesn't mean you can't get sick."
SENDING ALL THE GOOD ENERGY I CAN.....
KIMMY
If not thats ok too...but give it another day. HUG to YOU!!
...I felt like throwing in the towel the first few wks but things have gotten much better for me since. In fact, I told my husband I was going to need some rewards along the way if I made it through tx. Got my 12-wk reward last week; a new ring. YEA! What a great husband I have.
...I did #13/48 this past Friday. You are so much further along than me. Hope you can hang in there but will totally understand if you don't feel you can. We'll support you whatever your decision.
... Good luck and hope you feel much better over the next few days.
This tx is probably the hardest thing I've ever done in my 47 years and I've had some struggles, like everyone else going down the road of life does.
I looked at my wife and kids -- they need me -- how could I quit because it was hell? I thought of all the good acts I am committed to doing in this world before I go and that kept me going on. I thought of those who don't respond to tx, those that don't make it and died. I kept going on for them. Win for humanity so we can rid people of this damned disease. Everytime I read of one of us that gets their SVR I rejoice. I don't know anyone from this board offline but you people are like a family to me and when one of you wins we all win. I thought of all those patients that came before the peginterferons were around, and the monotherapy folks, that paved the way for us to succeed. Their memory demands justice. All of our individual fights against HCV is a way of honoring them.
Don't give up. Keep fighting. It is life you're fighting for. You're sure no loser -- no one going through this tx is a loser. They are people with a lot of courage and that is you.
You or your doctor don't know if your sides will get easier but from everything I hear and have been through during 48 weeks of treatment sides do come and go.
Get through today.
Maybe tomorrow the sides will let up.
Try some extra vitamins they sure helped me.
Tom
Man I am losing my hair like crazy also that is tough on my ego. That was one of the main things I had going for me, but oh well it's only hair as for the other sx's please ask your dr for help. I have wanted to quit many times and the most recent is that at 24 wks I was not clear but at 30 u/l. Man that really got me down. But with the help of the people here I am trying to stick it out. Please try and hang in. There are people here in maybe a lot tougher places not to make light of what you are goint thru.
Hang tough you can do it.
Peace
Bob
So sorry to hear things aren't going so well for you right now. You're one of the people here that have been my biggest inspiration & given me the strengh and attitude I needed to get this far.
Whatever you decide to do, I'll support you all the way as will everyone else on the Forum....it would be a shame if you quit as you've come so far...but with everything else going on....TOTALLY understandable.
Keep your chin up Dallas...we love ya!!!
Sending lots of love & hugs your way
Louise
Tom
ambush :)
Are you taking something for pain? For depression? Please be ok, we newbies need you.
hello, a month ago i had just finished shot 53 in 49 weeks and thought i had only 3 to go..my doctor suggested that i go an additional 2 months because it took me 16 weeks to test negative.i was crushed and upset..i had experienced very mild physical sides but had headaches constantly and major depresion and brain fog and severe lack of focus plus the fatigue...in 49 weeks i only missed 2 days of work...i was so anxious to stop...i found this forum and listened to many people to hang in there and go for it because this may be my only chance to kill the dragon...i kept reading theses threads and realized im not alone.my doctor is very aggressive and im thankful for that...i have now to date done 57 shots in 53 weeks,but with so much support from here and digging down deep to remember why i started this hell was to kill this dragon for good i am now anxious to do my next seven shots ....hang in there ....this fight is alot mental, adjust and dig down deep. but i do understand being ready to stop all together...we are not alone and have a great support system here.we can do it
good luck and god bless us all
Hang in there honey, berlynn
Love, Peace and Happiness
remember dragon slaying can be very hard work but i know you are up to it. Us dallasites have some real grit in our craw and I want you to use it and keep going. In the mean time i will pray for god to either give you more strength or to take some of the sides away.
I don't know what else to say or anything else I can do.
oh yes I will also ahve my wife put you on her prayer list and I will add you to our list at church. hang in there dallas tough(oak cliff tough even).
Sambone
P.S. If you keep going i will slice a hunk of green cheese off the moon and send it to ya!!! HAHAHAHHA!!!!
i also have leukemia and plan on starting the interferon at the end of feb. my geno type is 4, stage 3 liver dmg with cirrosis.
as far as i can find out you and i are the only ones posting here that have both hepc and leukemia.
i already have many of the sides that one would expect from treatment and haven started yet.
but what are our options dallas? ? we can give up or fight.
i choose to fight.
i might be a bit luckier than you in a few things though, i'm
a trauma tec in an er and the wife is an icu nurse, so we have access to a bit more help than most.
i have found that haveing my wife hang an iv of lactated rinngers with multi vitivitamin a couple of time a week helps
with my symptoms, of course most people dont have a wife thats a nurse and access to iv fluids, so i'm very lucky there.
but are you hydrating enough? ? from other posts i have read here that seems to be one of the best ways to deal with the sides.
not meaning to pry but do you have a port for your leukeamia treat? if so ask you dr. about iv fluid therapy it helps me so far.
as i approach my treatment date( should get it today when i go see my dr.) i will keep you posted as how i am doing, but hang in there dallas we can beat the dragon.
take care and i will offer prayers for you(pagan ones if you arent offended).
Starla
I WILL BE DOING INTERFERON 3 TIMES A WEKK FOR 48 WEEKS, I KNOW THIS SEEM TO BE THE OLD WAY OF DOING TX BUT THE CHIEF OF HEPATOLOGY AT TULANE UNIV. IN N.O. THINKS WITH ,Y OTHER PROBLEMS THIS IS THE BEST OPTION FOR ME (NONE OF THE GASTRO GUY'S IN AREA WANTED TO TREAT ME BECAUSE OF THE ITP, THYROID, ADRENAL GLAND, AND LEUKEAMIA).
THE DR IS WORKING CLOSE WITH MY ONCOLOGIST FOR MY TREATMENT AND ACTUALY I WILL BE RECIEVING TX FROM ONCOLOGIST, BUT GASTO GUY WILL BE OVERSEING TX.
I'M LUCKY IN THAT I HAVE A TOP NOTCH ONCOLOGIST THAT I WORKED WITH FOR 15 YEARS BEFORE HE WENT INTO PRIVATE PRATICE SO I KNOW JUST HOW GOOD A DR. HE IS.
DALLAS ARE YOUR GASTRO AND ONCOLOGIST WORKING TOGETHER ON YOUR CASE?
I HOPE YOU ARE HAVING A BETTER DAY TODAY AND PLEASE KEEP US POSTED AS TO HOW YOU ARE DOING.