Pegasus in dallas
Common Questions and Answers about Pegasus in dallas
pegasys
Not in Dallas but I'm in killeen...lol also I'm 23 but we do have on thing in common I'm having a baby girl as well!!!
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 ?
HI selmaS, thank you so much for being so helpful. We live in Dallas. Although we are seeing PD neurosurgeon, would you please provide a Dr. list for Dallas? There may be one them who's a PD.
In addition, where can we go to test if my son has EDS? Since opening dura is an option, according to what I read hear, it's necessary to know if the patient has EDS?
Is there anyone's kid here that has the same experience (open dura)? It sounds very scary. how's the recovery and result?
Karen Lee, also with Presbyterian Hospital Assisted Reproductive Technology (ARTS) in Dallas, and got pg in the first cycle with twins! I did meds and IUI, no IVF, but they are awesome! Dr. Lee is so cool and a genius. Her profile page is http://www.dfwivf.com/fertility-specialist-lee.html
Let me know if you have any other questions about Dallas, or doctors here. Happy to help!
One of the reasons I want to change doctors is because my current doctor in Dallas has made me do FOUR urine screens in as many months. I have no idea why they are doing this to me. Each time the screen was fine, but for some reason they keep making me give them urine. It's a really big hassle. I know they have strict rules about how to administer the strong narcotics, but I personally think that 4 drug screens is outrageous.
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.
I was recently diagnosed with a large cyst (5cm) on my left lobe and 2 small cyst on right. Both benign. My questions is I have a constant sore throat and pain in neck and also indigestion/ in stomach every time I eat. I am convinced its my thyroid issues. The endo doc decreased my Liothronine from 37.5mgcg to 20mcg because of side effects. The last thing I want is surgery.
Do others her experience these stomach pains/nasusea/sore throats.
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.
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?
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