I hear your fear and frustration. Unfortunately the doctor will have to tell you what it means since it would be impossible to figure it out over the internet. P.c.o.s. is no fun. When do you hear back? Can you call the doctor's nurse to get a report? Can your primary care help you with the pain? I hope you do not need surgery as well.
Alex
Iv suffered with this problem p.c.o.s for meany years now and its starting to get me down. I have a doctirs apointment on 30th january as I rang up today for my results and they said I had to make an apointment as the doctor eoukd like yo see me. Im just constantly in pain and it feels like my insides are twisting and feels like iv got pressure. :-( I just dont no whatvto do no more :-(((
Pain is no fun. Can you go to a pain clinic if nothing else?
Alex
I have stuff to take to help me with the pain. X
I hope you get relief from the pain. Keep pushing until you get an answer which makes sense. I wish I had a better answer.
Alex
Its just nice to talk to someone thats going or bin through the simler thing. Just gotta get these next two days out the way and im back atvtge doctors. Iv been told by people to go the hosputal but this tine round I feel scard for some reason.
I can understand your fear. I have Multiple Sclerosis (a neurological disease) and Stage 4 Ovarian Cancer. I used to hate hospitals and doctors. I have literally seen hundreds of doctors since I was two and the Multiple Sclerosis started. They are just people who studied medicine. I used to shake when doctors examined me. Now I realize they are there to help me. I try to learn all the staffs' names. The nurses and receptionists. It is a fun thing to do. It also makes you friends because people like it when you call them by name.A simple trick is to notice their name tag and use their name.
I am scared but I have learned courage is being afraid and doing something anyway.
I care and am sorry you are scared and in pain.
Alex
I have just recently been diagnosed with chronic lymphocytic leukemia (CLL) and they also found an enlarged ovary. I'm waiting for other tests on the ovary and one of two possible kinds of surgery...depending on what the ultrasound finds. So, I'm in the waiting stage myself.I'm really glad to have found this site so that I can talk with others like you girls. It's really difficult when we don't get all of the answers, which is so very typical of medical professionals. Thank goodness we at least have each other in this particular support group for help. I thank you and I will be there for you too as much as I can. I guess we will be back together fairly soon. Thanks, girls!
I much admire you fortitude. My daughter was diagnosed with MS at the age of 27; she' s 44 now.
Her father also had it, but died from a heart attack.
God bless you.