yugioh pegasus vs yugi

My boyfriend likes playing yugioh -.- idk why out of the years we've been together he's never mentioned it or played it. & he plays with his big brother.. well the last couple of days hes been playing for hours & doesn't spend much time with me & it pisses me off.

Just a simple question....i know if one decides to go another round of tx if one relapses, one should switch to the "other" interferon,which for me would be the pegasus...is there a static out there statingthe difference in SVR outcomes between the two in relapsers?...

i also watch foods i shouldnt eat and if i do eat them its only a lil bit, i dont drink pop that much maybe a can every few weeks, I bowl almost every saturday i go to places to play card games (Yugioh mostly yes im a geek lol.) and im not that much of a sports person due to ashma and heat dont mix so yeah. So does Anyone know what i should do?

I am 22 yr old and i have hepatitis c genome 3 and i am taking pegasus\once weekly and ribavirin since 19-6-08 my question is have i to do weekly CBC or I can do every 2weeks before the injection ?

I was pissed when my hubby left me to play yugioh cards lol he was paying no attention to me! I sat him down & talked about it & he started changin that.. its not the same as your situation but sit him down & talk about it & if he doesn't wanna listen tell him you're trying to save your relationship & if he doesn't want to, to let you know & if he does tell him he needs to start communicating more.

Pegasus and Dr. Lupo, I have almost the exact same thing. I have a multicystic nodule on my left thyroid and every now and then i get a pain in my neck followed by a minor sore throat and some hoarseness due to a cough i usually only get when it flares up. I recently have been getting an upset stomach almost everytime i eat and i thought it was due to my acidic levels.

Hi, I'm new here, and my husband is in his 10th month of treatment. Just had his second transfusion, and he isn't bouncing back. They upped his procrit, and he has had to stop taking ribavirin again. He's still on a half dose of pegasus and his viral count is undetectable. His doctor said he hated to pull the rug out from under him last visit, and it looks like I"m going to have to take him before his next visit. I think he may need another transfusion soon.

Will the Pegasus work without CoPegasus, I'm getting alot of side effects, I cant sleep and itchy rash's, I can handle the Pegasus alone but the Copegasus makes me feel bad. My liver function test are normal. Has anybody gotten rid of the hep without it?

I have had ascites but it is now under control. My hepatologist has ordered Pegasus and Ribo for me. He says that I only have a small window for treatment success (which he says is probably very low 20-40% if that) and I am wondering whether it worth going through the side effect and complications. I also have a long standing history of dysthymic disorder/personality disorder. My Rx is ready for me to pick but I am reluctant. Any comments.

Just got my Pegasus and co Pegasus.Was hoping just for just the Pegasus, But there was a study that said non responders faired no better than responders on there study. Why this applies to me I do not know. I am a relapser. This cost the insurance company big money. Any Ideas? At stage 4 i have no time to wait. Have had the same issues getting into the studies. Relapser. Life can be hard at times.

I I will be taking pegasus soon.can my wife be subjected to any of the drug through oral sex with me ?not a joke question.

Since every patients profile is different, their metabolisms differ, they drugs they take differ….so the complexity of helping vs. killing them is very real. Since some inducers have been observed creating 100 fold increases in plasma levels, it is imperative that the patient NOT attempt to improve the synergy of any drug without the knowledge and approval of his or her physician.

After 3 weeks post pegasus/ribivarin (48 weeks responder so far) still suffering with rash, body aches, migraines, insomnia. My energy level is improving but is not great.

Hi I am Viktoriya.First week of treatment with PEGASUS and COPEGUS -feel very bad :fever, headaches, body hearts like- flu but stronger,feeling dizzy. Is it getting better after first week??

I am soooo annoyed with the fact that my bf is 26 years old and plays yugioh cards. He plays every single day and even goes to tournaments! He takes it so serious and is so passionate about it that i dont know how to tell him how much it annoys me! I hope he stops by the time my baby comes. Its just so childish to me!! He even talks about it on the phone with me and i get so mad and he just dosent know how bad i hate it!! Should i tell him??

Which one would you all recommend she go on, the Incivek 12 weeks plus Pegasus 48 or the 44 weeks Victrelis plus Pegasus 48? I think the Incivek has a few more sides but a better success rate. Is that true. Do patients with a lot of Incivek sides normally improve after the 12 weeks? Any info to help in the choice would be great.

6 million and started with Pegasus and Ribovarin Therapy at third month my pcr become –ve I left the treatment after 24 injection but after 35 days of breakthrough when pcr become +ve I started the treatment again . now I getting Pegasus and Ribovarin Therapy . my question is that at this moment I have taken 28 injection .

I am about to start Pegasus and Ribovarin Therapy for the second time. My doctor said that I may not have been on this Pegasus and Ribovarin Therapy long enough the first time. I did it for 11 months. would be interested to here opinions of what myi chances are of the treatment being sucessful this time around. I was really suprised that it come back. The first time I did the treatment I became anemic and looked like a ghoast until I was able to start procrit.

Yugioh pegasus vs yugi

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