Complaining research

Common Questions and Answers about Complaining research

complaining

I wish people stop complaining about what questions other people post... Either read it or don't! answer it or don't! I know this may seem hypocritical cuz i am doing the same thing right more but whatever! Don't read mine either!

Thanks for the link. It is a lot of information. I do agree with the findings. The doctors here need to get on the ball . We need help and fast. There is so much research that needs to be done. I hope and pray it will be done soon rather than later.

So since I found out I was pregnant I've been looking on craigslist and eBay to help me find used baby things to buy for the baby, we're on a budget but I want to be able to get my baby what he needs without depending on other people and ever since I started doing that my bf has been complaining.

Why is it that science and medicine research so much on synthetic chemicals and such yet all these natural items: primerose,cinnamon,aloe era,cumin,etc.... That many of us read on pregnancy website for induction for example haven't been researched the heck out of them? There's so many natural item that by now and how technology is and our advanced medicine that we don't know all about them.

Greetings doctor I am actually doing a research paper on HIV for school and with so much info online from one end of the spectrum to the other I figure I would ask a specialist directly a few questions so here it goes... 1-with testing now a days would you consider 6-8 weeks conclusive? 2-do you believe rapid tests are just as reliable as lab based? 3-do you feel oral rapid tests are just as good as blood? 4-what are the most common symptoms you see with onset of HIV?

I know somebody posted where to go to find out about the research that is going on, and what clinical trials we may be able to get into... but my brain isn't working today and I can't find the post. Somebody please give me that web site. I'd really appreciate it.

Gene therapy has potential, not to recreate lung tissue but to reduce the airway inflammation that results in emphysema, be it smoking-induced or other. Research is underway on gene therapy but the results thus far have been very disappointing. The adaptation to chronic residence at high altitude has been studied extensively. You are correct in stating that bigger lungs have nothing to do with it and that has been well known for nearly 100 years.

is there a research group one could participate with, study and analyze past, present and future findidngs/options? i have been outbreak free for years and am almost certain i recently had my first outbreak in january - and they won't stop. i think the following has provoked the virus, as well as disable the latency stage: a. i took a strong proton pump inhibitor in january for my gerd - within a week i had a broken tail bone and rash of blisters across the bottom of my back.

Found out he was cheating on me the whole time he was complaining about me not sleeping with him. He's gone, I'm better off, living the stress free life!! Happy and single!!!!

LOL! Thanks Ladies! I keep trying to remember, it will be all worth it in the end! Lord, what we endure to bring our children into the world.

Mods - could you please explain where to post on HepC issues because one forum is "Hepatitis Social Community" and the other one is "HepC". I've been on the "HepC" one but had two messages moved to the social community one today. Don't know why. I think it would help all of us, NOT that I'm complaining because these forums are a lifeline - a REAL lifeline - but could some clarification be given to us? Thank you.

For all the "regulars" that have indicated an interest in public access to the research papers that Dr. Kutryb and I are doing based on these websites and also the problems with multifocal IOLs use this link. Cut and paste in your browser. http://www.revophth.com/index.asp?page=1_14244.htm John C.

Due to chronic pain and unable to walk and stand and a variety of other symptoms, I finally got an MRI of my lumbar (I've been complaining of my pain in my sacral though) and they found a tiny CFS cyst. The neurologist suggested Syringomyelia but when it didn't go higher into my thoracic he said it wouldn't be causing me any symptoms (I'm in a wheelchair from pain) and I was fine.

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