Well sorry it has taken me so long to write this entry. My appointment was on Wednesday and it is just now that I can kind of get my head around what we were told.
I got the morning off work and Chris and I headed to the Queen Elizabeth Hospital in Kings Lynn. It is about 40 minutes away but they were the one that could get me in the soonest so that is where we went. We parked up the car (and had to pay to park!) and walked to the appointment. As we were walking down the corridors there were all these pregnant women walked past me and I couldn't help but feel like it was a bit insensitive to have the infertility office at the same place where we could be bombarded by everything we were hoping for but everything that was just out of our grasp. While sitting in the waiting room I looked around at all the posters of babies all over the wall, all the women rubbing their bellies, and through my whole wait I could hear babies heartbeats coming from the back rooms where they do the ultrasounds - it was a long wait.
Chris and I did finally get called back to see the doctor. He asked us several questions, very personal questions (I figured) and then said that they first rule out if it is a "mechanical" problem. He said he needed to do an exam (I figured that too). Poor Chris, has never had to deal with anything like this in his life. There was the exam table, and a chair by my head and two down nearer my feet. Chris went to sit on the ones near my feet and I firmly suggested that he make his way up nearer my head, "but I wasn't going to look," he says - I explained to him that I would just feel a lot more comfortable with him near my head.
*Warning
Girly Details*
see anything with this rubbish machine," and directed me to wrap the sheet around me and follow him to another room with a newer machine. Chris opted to stay in the room and let me go this part on my own. I got to the other room and he repeated the internal scan this time with a machine that looked like it was made in the current The doctor did a regular examination taking lots of swabs to test for different things. All the while telling me to "Relax" the most useless word at a time like that. Then he decided that he would want to do an ultrasound to see if there were any cysts. I figured I had had an ultrasound before when I wasn't well, so, that would be fine, I gave my permission. Then, to my horror I see him pull out a probe of sorts, it was at that point he told me it would be an internal scan. I will spare you the gruesome details suffice to say, the first part of the exam was a walk in the park. While he was doing the scan he looked quite concerned and said he, "couldn't tell anything with such a rubbish machine," and asked me to put the sheet around me and walk down the hall to another room. While in there the whole internal scan was repeated, but this time with a machine that looks like it was made in THIS century, not a few past. All of the sudden he started printed pictures like mad and asked the nurse to go get the head doctor. She came back in and said he would be right there so we just waited... in the middle of the exam we just waited for 5 minutes, then the nurse told us he was on the phone and she'd go check again... then we waited some more. Finally the other doctor came in and looked at the screen and confirmed what the other doctor had suspected -
endometriosis caused by 2 cysts. He asked me to head back to the other exam room and wait.
I went back in and got dressed and waiting for the news. Cysts, from what I've heard are easily treated. But then, that is with American health care... NOT the
NHS (nationalized health care -- JUST SAY NO!). The first doctor explained it like this, "You have two cysts - one that is 5 cm on your left side and one that is 2 cm on your right side. There is some blood in the one on your left and this cyst is causing your
endometriosis. We will have to do surgery and because you are heavier, it will be an in-patient surgery. The wait for this surgery, if we put you on the list now, is 12 - 16 weeks. After this surgery (and maybe during, depending on how well it goes) we will need to inject dye into your Fallopian Tubes to see if the cysts have made
adhesions, causing them to close up and not release an egg. If we cant do it at the same time, you'll have to be put on a waiting list for this."
Enter head doctor... he says, "Because you are heavy we will not operate until you loose 2 stone (upwards of 26 lbs.) We will give you hormones to stop they cyst from getting bigger, set up an appointment in 4 months and then we'll see how you are doing. If you are loosing the weight we will THEN schedule you for surgery and put you on the waiting list. You see, the
NHS wants value for money , they wont operate or help anyone unless it is 'worth their money'."
Tear my heart out....
The doctor sent us on our way to make an appointment for September - problem is, there are no available appointments in September, so now we are into October.
So that is how it went, now would you like to know how I feel?
I HATE that the problem could be easy to fix but, because we use the
NHS they wont help us right now.
I HATE that we are looking at, a min. of about 2 years before we can even TRY.
We are not telling people about the fact that I have to loose weight (and by people I mean people near us), the last thing I need is people analyzing everything I eat.
I, somehow, am going to have to get used to the fact that for a while a baby cant be in our life plans and that makes me really sad. I don't know how I am going to do get used to it. I also have to become less
sensitive and realize that people
don't say things just to "rub it in my face". I
don't want people to have to walk on eggshells around me.
We have had several people who we've told us miracle stories of people who had cysts who had babies... we know, we know... but it wont be us, the problem is too big right now and to be honest it isn't what we need to hear.
Adoption was always something we considered, but with the laws for immigrating a child to America that, right now, is not an option.
We were going to foster care, but I got a phone call today and the woman said that until we have a 2 bedroom place (read: more money that we don't have) we will never be approved.
And to be honest... all I want right now is to be in America, with my family and friends, but I am stuck here and it looks like unless there is a free house we could move into, and a job waiting for us - this is where we'll be for the medial treatment - and here I'll be childless, lonely and missing home.
I know that is quite negative, but it is going to talk a while to see the positive.