Constellation pegasus for kids
Common Questions and Answers about Constellation pegasus for kids
pegasys
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 curious so I went to Klinghardt's web page and searched "Group Constellation Therapy" and only came up with "Family Constellation". Maybe you can try searching his web page and come up with something.
Although I visited ophthalmologist for this question I was not persuaded that Pegasus would not interfere my Uveitis negatively. On the other hand, hepatologist told me that I may take corticosteroids if my Uveitis gets worse.
I saw the post by Willy50 in this thread http://www.medhelp.org/posts/Hepatitis-C/HCV-Clinical-trial/show/1414377 .
So please does anybody knows something about this? I mean corticosteroids plus Pegasus ?
I feel like I have been hit by a truck migraines hot cold just a daily hangover on steroids. I am a non responder to Pegasus and switched after 4 months and have been on infergen for almost 2 months. It is working and I feel blessed just wondering how other people get by when it feels like you just can't get a moment of relief getting up to grab my son from getting into things is a challenge. I'm ready to give up please help on how you made it through....
I don't go to the doc for another 10 days but I've been doing some checking and I'm not sure if I'm gonna be able to pay for treatment. I have transitional medicaid and it pays for 3 scripts a month. But I don't know if there's any limitations on what scripts it will pay for. Has anyone here been able to get on any government disability programs like through social security or through the state? Does anyone have any info on programs to help pay for meds?
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.
The nausea and stomach pain is not typical for thyroid cysts/nodules -- however trouble swallowing, neck pain, cough, and hoarseness may be due to the cyst. Would consider treating with an antacid (eg zantac or pepcid AC or prilosec OTC) - as acid reflux would potentially cause all your symptoms.
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?
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.
Zaydin is nice. Also a new one for you : Jaxyn...
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.
I am going into week 3 of my treatment for hep c,I'm currently on pegasus,ribavarin,and incevek (telapravir) anyway my queston is I usually take it 10 in the morning and 7 or 8 at night. And I wanted to know is there a time limit for how many hours apart?cause the bottle just says one in the morning and once in the evening.anyway let me know.
This feeling made my chest wall feel tight and constricted and made me feel like I could never get a good deep breath of air, and all the time my chest felt as if it had a weight inside of it. This symptom lasted for about 6 weeks, and then started to improve (but not go away completely). When the improvement started, I started feeling very lightheaded constantly and disconnected from my surroundings. I will have headrushes and vertigo spells where it feels like I may faint briefly.
This feeling made my chest wall feel tight and constricted and made me feel like I could never get a good deep breath of air, and all the time my chest felt as if it had a weight inside of it. This symptom lasted for about 6 weeks, and then started to improve (but not go away completely). When the improvement started, I started feeling very lightheaded constantly and disconnected from my surroundings. I will have headrushes and vertigo spells where it feels like I may faint briefly.
I would see a doctor about these symptoms if I were you. There are many ailments that can cause this constellation of problems and really can't be diagnosed without appropriate testing.
hello all,
i have a question regarding ARS, i know that symptoms do not mean nothing but can just one symptome like fatigue for 4-5 days be ARS?or normally is a constellation of symptoms?
Seeing that there not doing any more trials in my area for Sofosbuvir I am now looking at Faldaprevir.Is anyone on a current trial with that right now.Also if you failed treatment with Pegasus,Riba and telaprevir would I still be able to do it?
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.
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