Sunday, December 27, 2009

Option B

When reading over that last post, I realize it is crazy-long. So, I present option B: A recap of the recap:

This year sucked.

The end.

12

With New Year's quickly approaching, I have been reflecting on the past year and wondering, "what did this year mean to me and what did I learn?" Because, y'know... that's why everything happens, right? To learn? Although it turns out that there are actually 12 months in the year, my year seems to have consisted squarely of 2. When I think of 2009, I am thrown into a deep saddness. I feel incredibly guilty that although many wonderful things happened too, I am so focused on the negative that I feel that that is all that occured. I am positive that 2009 was the worst year I have ever experienced. Let's recap:

January:
We went to Disneyland on a family vacation. We were having the time of our lives until I succumbed to my addiction and peed on a stick. Uber faint line. Happy? or Sad? Hmmm, guess we'll find out.
When we got back, I entered beta hell within hours of getting off the plane. Depressing numbers all around.
February:
Miscarriage #2 within only 10 months of my first. It was a great way to start the year.
March:
Celebrate my 9th anniversary with DH.
April:
Perfect ovulation. Day 14. Too bad I was still in my 2 month "probation." My RE won't let us try until 2 complete cycles have passed after a miscarriage.
May:
LJ turns 7. We celebrate by getting her the cuttest birthday present ever. A rex rabbit. Actually, I celebrated a bit much and got one for myself too. I couldn't resist. They are just too adorable!
June:
No ovulation for me. My car is "out of commission" until we can save what seems like a million dollars to repair it. So glad I'll be couped up all summer for lack of transportation.
July:
Still not ovulating. I have now slipped into the seventh circle of hell and begin fighting a depression to put all others to shame. I am no longer sleeping, I have no energy, and I am feeling like a worthless individual, in addition to the world's worst mother and wife.
August:
Still super depressed. 3 pregnancy announcements in 1 week. 2 of which were my SILs. LJ goes back to school (I miss her.)
September:
I have a miraculous ovulation... FINALLY! We go forward with IUI #7. This makes me much happier than I have been for months. Happy enough to not really be too bothered with another pregnancy announcement by a SIL.
OCTOBER:
May very well be the worst month of my life. Beta hell ensues. A total of 9 draws (beginning at 13, ending at 790) and 3 ultrasounds. Progesterone injections everyday, 3 discussions with REs/OBs all ending with "you are going to miscarry." Morning sickness from hell, all knowing that it probably was all for not. The ending of the month was spectacular. A ruptured fallopian tube with severe hemorrhaging, and me being forced to allow a doctor that I had never met before to end my baby's life. I know... he wouldn't have survived anyway, but now I feel like I LET it happen. I am just now starting to remember things from that night that I am sure my subconcience was trying to hide forever. My pleading with God to let it all be a dream, to please let me have my baby, and apologizing profusely to the child I would never meet. Good times.
NOVEMBER:
Recovery is not easy for me. I am in a lot of pain although the Dr. insists that I "shouldn't be." More ultrasounds with the stranger Dr. and his reassurance that everything is fine. My beta dropped to 55 after surgery, so I should be back to normal in "no time." Then normal shatters. My beta begins to rise again, and that night I am back in the ER with a severely distended abdomen, and a small amount of pain. 6 hours later, I am in an ambulance being taken to a better hospital for another laparoscopy to repair my right tube, AGAIN. Diagnosis: Persistent Ectopic Pregnancy. I leave the hospital after a double dose of Methotrexate. Lucky me.
December:
Medical bills eat Santa's budget, and family parties steal my Christmas joy. I am astonished at how insensitive family can be. I really thought "I don't want to talk about it" was a pretty clear declaration. Apparently inquiring minds want to know, and will not settle for a teary plea to leave me alone. 3 SILs all happily sporting a pregnancy glow, while I feel like the black hole of the family. My RE put me on birth control that steals what sanity I have left and leaves me going through maxi pads like crazy. All the begging in the world will not convince my RE that I can do another IUI my next cycle, or that I can do without the birth control. The medical cloud is lifting and I am starting to remember more and more that not only was this horribly traumatic for my body, but that I LOST ANOTHER BABY. One that I am told again and again "would probably have been a healthy pregnancy if it had implanted in the right place." I know that those words are meant to be encouraging and give me hope that the "next time" I can do it. But instead, it leaves me incredibly sad. Another failure. This time my body murdered my baby. This was not my baby being "genetically abnormal", or that "something just went wrong with the embryo's development." This was caused by MY body.

Last week I met with my RE again. We discussed our plan for the new year which consists of an HSG sometime around the 10th, followed (hopefully) by an IUI in late January or early February. I will again be on the progesterone injections, and if God be willing and I manage to get pregnant, heparin injections twice a day.

I am so ready to move on. I can't bear the thought of another year like 2009. I don't think I would survive it. There was just too much heartache, so much of which I will keep to myself. I have so much more bottled up inside that I want to let out, but know that it will just come out as more rambling that makes no sense to anyone but me and make me sound even more unappreciative of the things that I DO have. I can't handle anymore. I feel so guilty for being so focused on the negative things in my life, when I have so much to be grateful for. My daughter and husband are the only things I have to live for. They are the only light I have left.

I guess some good did come out of December. I was finally able to get a referral to a counselor that specializes in infertility. Let's hope she can handle me. I am really looking forward to meeting with her.

On to 2010. May it be a year full of all the wondeful things that I thought I'd never get a chance to experience again, and to all of you who deserve your Happily Ever After's even more than me. I owe so much to all of you that have been here for me through everything. You know who you are. I am eternally grateful for your comments and emails. They mean soooo much to me.

Best wishes to you all.


Sunday, December 13, 2009

Booooring

I just wanted to let you all know that yes, I am alive. I just don't have anything to write about. My RE put me on birth control pills (because it's SO likely I'll get pregnant on my own *rolls eyes*) for this cycle and at least 1 more. I then have to go in for another HSG before we can get back on the TTC bandwagon. So, in short... I'm in limbo. Sleepless, frustrating, hormone induced limbo.

I can't wait for 2009 to be over. So long, worst year EVER!

Oh yeah, and if you were wanting to see the surgical pics from my ectopic, here is a link:
http://picasaweb.google.com/ItsJustMeim/Ectopic?feat=directlink
They are not for those with sensitive tummies. You've been warned.

Thursday, November 26, 2009

Thankful

Happy Thanksgiving, Everyone! I hope you have a wonderful holiday weekend and that the turkey isn't the only thing that will be stuffed by the end of the day.

In light of the occasion, I thought it appropriate to list a few things that I am grateful for. I know that I am blessed beyond measure, but it never hurts to try to recognize those things in our lives that make us happy day in and day out.

My short list, including the things that I am MOST grateful for:

DH - He has given me my 2 most precious titles; Wife and Mother. Eternity truly isn't long enough to spend with this man. He holds my heart and nurtures it everyday. I love him with every ounce of my existence.

LJ - No one can make me smile like she does. She is brilliant in every way, and makes me proud beyond measure. There are no words to express the love I have for her, and no greater blessing.

My inlaws (brothers, sisters, and parents.) - Even though I sometimes get frustrated, I must give them credit where credit is due. They have taken me in as a part of their family so completely that it is hard to believe that I am "just an inlaw" to them. I know that when it boils down, any one of them would walk through fire for me. Not many people can say that. I am so thankful for the love that they show me. I love each of them so much.

My friends - Both IRL, and here. I have felt so much support in all that has happened. Since my second surgery, I still haven't had to make a meal for my family. My friends and neighbors happily volunteered to bring us dinner for the last week, with plenty of leftovers to tide us over through lunch the next day. We have been served with the most dignity and grace imaginable. We have felt so loved. Although most don't really "get it", they do what they can to lighten our burden. We have been so deeply touched with kindness from all directions. To all of YOU -- thank you for always being here. It helps me more than I can ever tell you to know that you all understand, even if it is on a different level. Everyone has different experiences, and yet we are bound together with a single thread. I feel so blessed to have been welcomed into this community, although we all agree that it sucks to be here in the first place.

I hope you all have such a wonderful day today, and that the celebration happily lasts all weekend. We all have something to be thankful for, no matter how big or how small. I am grateful that I am able to recognize my blessings, and thank God for them everyday. Thank you for being one of my blessings. I am sincerely grateful for each of you, and for the friendship you so readily supply. Please let me know if I can ever help any of you, in any way. I am glad to do it. Whether it be a late night stressfest or just a virtual hug, I'd be happy to be your "person."

Happy Thanksgiving!

Saturday, November 21, 2009

Moving on...

I think this might be over. I don't want to jinx anything, but I'm feeling pretty good. I was scared to death for the methotrexate, but so far I haven't really had any major side effects other than mild headaches and nausea.

I didn't really post a lot of details because, well, I don't really know them all. So here's what I do know: (It looks like a lot, but it really isn't. I am full of questions)

*On Tues. morning at about 2 AM, I called nurseline to see if the pain I was having could potentially be caused by me ovulating in my recently operated-on tube. The nurse went through a "check-list" of symptoms if you will, and threatened to send an ambulance if I didn't go to the emergency room ASAP, or call 911. By 2:30, I was at the local ER

*By 3 AM, Dr. Dumbass (sorry, there's really no other way to put it) had ordered a CT with contrast, and insisted I chug what seemed like a gallon sized mug of lemon flavored fingernail polish remover. It was delish!

* 5 AM, still no sign of the Dr. or the nurse to update me on what was going on. I was FREEZING, because I was in the room closest to the exit, and it was quite drafty. Now would be a good time to mention that there was NO CALL LIGHT!

*5:30 AM, I am taken in for my CT. I am done about 10 minutes later and wheeled back to my igloo.

*5:50 AM, Dr. Dumbass comes in with my results. He tells me that there is a "significant amount of blood and free fluid in my abdomen" but that he isn't trained enough to know if it is old blood, or if I have re-ruptured. He recommends that I follow up with MY doctor later that day, or tomorrow at the latest. He then seems to second guess himself and asks for my Dr.'s contact information. I gave him the info for my RE, and he exits to call him.

*6:00 AM, Dr. Dumbass comes back and says that Dr. Peterson would like to see me today for 2 reasons: 1. My beta is continuing to rise, and 2. There shouldn't be this much blood in my abdomen so long after my first surgery. My body should have absorbed anything left over from my first go around. I ask him if I need to go out to the clinic, or if I should meet him in the hospital. Dr. Dumbass explains that I cannot be released on my own accord because I am at significant risk of "bleeding out", so the ambulance will be there to transport me within 30 minutes.

* I stop noticing what time it is, and call DH. He is at home with the Munchkin, and doesn't think anything too serious is going on. He was pretty upset when I told him I was waiting for an ambulance to transport me out to the U, I think he realized a lot sooner that I did the seriousness of the situation. By the time he got there, the ambulance was waiting. They let LJ ride out to the hospital with me because we knew that once I arrived there, she would not be allowed to stay. No one is allowed in the hospital that is under the age of 14. (we SO broke that rule...)

*Once we arrived at the U, I was brought to my room and prepped for surgery. Blood was drawn, my IV was replaced (more on that later...) My RE came in and went over the plan with us. He said that he was 90% sure that he would have to take my tube. I had a mild breakdown and begged him to leave it in. He wouldn't budge, but told me that he would call DH after they opened me up and could get a better look at the damage. He said that they would wait and let DH make the decision once they were in there. This is about the time that I lost my freaking mind.

*Things get pretty blurry, but I remember my brother in law being there, and he and my husband giving me a religious blessing. I then threw a fit and insisted that they let LJ rid on my gurney with me down to surgery, where I would say goodbye and let my brother in law take her home with him. Once we got down to surgery, they had to change my IV (AGAIN; this was my 3rd) and the anesthesiologist explained what they would be doing. I vaguely remember kissing a tearful DH and them wheeling me away. I don't think I even remember getting to the OR.

*We're going to skip the waking up part, because it was probably one of the worst memories that I have the privilege to carry with me for the rest of my life.

* I was taken back to my room where I was told that I almost bled to death... again. My body had gotten wise to this fact at some point in the previous 2 1/2 weeks and had taken measures to prevent it from happening. The omentum (I still don't know how to spell that) had moved forward and surrounded my fallopian tube tourniquet style and had slowed the bleeding. Once my Dr. and his minion of medical students had seen the damage in my abdomen, and the omentum around my tube, they called for extra blood and another IV was started in my NECK!! They were sure that I was going to bleed out, so they started the extra line to be able to get fluids and a blood transfusion in me quickly if they had to. Luckily, the bleeding was controlled and they were able to use suction to clean up my insides. They cut my tube length-wise and flushed it in both directions with saline. The Dr. had kept his word, and called DH and told him what they had found. At that point, he was positive that he would have to take the tube. DH told him that we trusted his judgement, and to do whatever he thought was best. We were stunned when he informed us later that he had saved the tube. He said "for good or for bad, we saved the tube." (At first I was really relieved, but now I'm not so sure how I feel about it. I'm nervous that it will scar up, and I'll have this issue again.)

*Later that night, an oncology nurse came in and gave me my methotrexate shots. I had one in each hip. They made sure to give me some Zofran for nausea before the shots, and I think that did the trick. It wasn't horrible at all. I am still not experiencing anything horrible. Just minor headaches and a bit of nausea from time to time, although I've read online that it can take a few days for the full affects of the drug to kick in.

*On Wednesday, my Dr. came in to release me at 8:30 in the morning. We didn't actually get to leave the hospital until close to 6 pm. The resident and my Dr. were arguing over which medications I could have when I came home. The final outcome was that I could come home with ibuprofen, zofran, and iron. No narcotics. (I'm still kind of pissed about this. I have 5 holes in my abdomen, and they expect me to be just fine with ibuprofen. Sadists!) My Dr.'s reasoning was that I am still at risk to have this happen again (at least until my betas drop to zero) so he doesn't want any medication to "mask" the pain that could be caused by another rupture. I understand his point, but man it would be nice to be able to move without cringing!

*My blood counts are still low, so I will be on iron for the next 30 days, minimum. I have to go back in every Tuesday for repeat betas to make sure my levels drop. I am not to take any vitamins or folic acid for a month, and because methotrexate (MTX) is a chemo drug, I have to avoid large groups of people, or places that I may be more likely to be exposed to illnesses. Apparently MTX is an immunosuppresant.

Okay, I think I have you all caught up. I have a follow up appointment with my RE on Dec. 1st. He has promised to give me pictures of the laparoscopy. I have them from the first surgery, so it's only fitting that I have pics to complete the series. I have debated on whether or not to post them on here, but I think some people might be a little queasy about it. You'll have to tell me your opinion. Is that something that you would be curious to see, or am I better just leaving it to your imagination? I still have a ton of questions about this whole thing. It all happened so fast that I don't think it all sunk in. It's hard for be to believe that my life was THAT jeopardized when I didn't feel that bad. I think I just need a play by play. I will be glad when I get the operative reports and pathology findings. My RE did mention that between both surgeries, he estimates that I lost about 2.5 pints of blood into my abdomen. I'm not sure how bad that really is... guess I'll have to go ask Dr. Google.

I'm pretty sure I'll post again about my experience at the hospital. They nurses (other than the first demon-woman that I had kicked out of my room) were amazing. They gave me a bereavement package that included a little crocheted blanket, booties, and hat, as well as a baby-sized brass ring. They were very kind, and I will never be able to thank them enough for their compassion. I am so glad that I was transferred to their hospital. I think they helped me begin to move on. They recognized my baby, and made me feel like it was okay to do so, regardless of how far along I was. I truly am grateful to them.

Please let me know if you have any questions, or can think of anything that would be good to ask my Dr. about. It all still feels very surreal. If I wasn't bruised from hell to breakfast, I might doubt it ever happened! (maybe I'll post THOSE pics! You've never seen bruises like these before! I look like a junkie!)

Again, thanks for all of your comments. IRL, I feel very alone in all of this. It is so nice to feel your support day after day. You are all very amazing to me.

Tuesday, November 17, 2009

Back in the hospital

So, here I sit, an inpatient at the University of Utah Hospital.

I ended up in the emergency room last night because I started bleeding again, and had some pretty decent pain going on. They did a CT scan with contrast. That's all it took

The next thing I knew, I was in an ambulance being transported to the U, and into the care of my RE (who btw is the Head of Obstetrics and Gynecology here.) I was hemorrhaging again, and my hematocrit was falling.

Again, they were able to save the tube, but this time not without cutting. I don't have the details of most of what they did, other than that the omentum (sp?) had saved my life. It is a fatty layer, that sits in your abdominal cavity. It had moved to wrap around my fallopian tube to "save my life", according to my RE. I haven't seen the pictures yet, but DH said they were really awful. My insides looked like they blew up.

Right now I am feeling pretty good other than some excess CO2 that is molesting my shoulders and chest... but the pain is managable. I am waiting for a methotrexate shot, and then I will be going to sleep. I haven't been asleep (other than surger, which TOTALLY doesn't count) since 7 am on the 16th. I am TIRED!

I will update again later. I'm sure the methotrexate will have a story all it's own. OH, FUN!

Monday, November 16, 2009

The Nightmare continues...

My beta rose today.

CRAP!