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Can I tell you a little secret?

I’m scared. I’m anxious. I feel a little like a failure…well a lot like a failure but we’ll get back to that in a minute. Thursday is the day we meet our second RE in the last 19 months. We just want a second opinion. Dr K.’s office says we can either go back on Lupron for another 3 months or have the worst periods ever and continue on that path until we are ready for IVF. At this point all my numbers are low. And by low I mean they are basically non existent. When I asked the nurse that works with Dr. K what to do next, like could we do a round of femara with a trigger shot and try on our own? Can we do the femara with trigger shot and then plan another IUI? I could hear the heartbreak in her voice because she said I’m sorry but the best thing you can do is to save up the month for IVF because no other is going to work for you. That’s when Russell brought up the idea of getting  a second opinion to see if they see something or have a different type of treatment that isn’t going to break the bank. What makes this harder is knowing nothing is wrong with Russell, thank goodness. His labs and analysis all came back extremely well and I am so grateful for that. But that means I’m the one that’s broken. And 13 months into a brands new marriage this is tough. I knew when we said for better or worse and sickness and in health  that phrase would ring so true over for us right now.

I know some people have asked about why we chose to see another RE (reproductive endocronologist) because Russell is all about asking questions. He is all about making sure we leave a meeting knowing every little detail before the paperwork has even come to our mailbox. I love that about him because in situations like we’ll be in I freeze and can’t think of anything to say. I just write down the answers and make sure we can discuss everything on the car ride home. We are also seeing another RE because I’m still in a lot of pain and I feel like I”m being heard. KRM is a great establishment with one of the highest live birth success rates. Dr. K. has been nothing but nice and straightforward with me and with Russell. But a second opinion never hurts because some doctors think more outside the box while others don’t.

I also don’t know if you all know this but Russell and I wanted to have 4 or 5 kids. In the very beginning stages of our relationship we would talk about how cute babies are and one day we’d have our own. Well Lena made her debut as a ‘Young’ about a week later. He thought I was taking her back but she was stuck with us and the other two that following. More about their stories in another blog. I got off on a tangent there for a second. My point is Russell and I have always wanted a large family. Now I’m not sure what we’ll have. We will definitely implant two maybe more depending on how we feel about it and see what happens from there. If somehow the universe will allow my body to make a few eggs we’ll let them become fertilized and freeze the healthy embryos in case we decide we want one more try at it in the future. Needless to say I’m sure you feel a little stressed reading this. This is what I go through on a consistent basis. Throw in some random questions like ‘why did Russell marry me know I have a disease that is incurable and children may not  be an option. And the am I pretty enough? Am  I good enough because with the way  I look and feel no man should have to look at it. But each time he says he loves me, he thinks I’m the most beautiful woman in the world and that children or no children we’ll be just fine as long as we have each other. Please send your positive vibes out for us this week and every week because infertility is bad but knowing it’s what you’ve always too is heart breaking.

Until Next Time

xoxoxo

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The little things make you realize how much you want a baby, but also how possible it could be for one couple and impossible for the other couple. I am 1 in 8.

I was watching one of my favorite shows, Eric and Jessie on E!. They were talking about whether or not to have a baby and if they’d try for another because they said it was easy for them. Her sister who was pregnant at the time said well how are you feeling? So naturally Jessie went to take the test. Eric walks in and is asking what they’re doing and he sees the test is negative. The next scene is the family hugging together saying it’s not meant to be this month. See that brought back so many emotions and I started crying. For those that haven’t caught on yet, crying is one thing I’m pretty damn good at.

But in all honest the memories of the TWW a few months ago were brutal. They were more than brutal. There were days that felt like they were drag on so slowly and we’d never get to test. Then test day comes and you don’t really sleep the night before because you’re so anxious you have to know. I am also a super type A personality.  I also remember wondering the entire time “are we pregnant?”. The first time I thought for sure because I was having some unusual cravings and then I was having a few pregnancy symptoms but the test came out negative anyway. That was more heartbreaking than my boyfriend in high school saying I was boring and he wanted to date someone else. It was more heartbreaking knowing my body couldn’t do it. Then the second time we did the TWW and I felt nothing. Not one symptom. No tiredness. No nausea. Nothing. And sure enough the test was negative. The feelings of loneliness and depression have been sinking in lately. The holidays are coming and I’m wondering what the next few months will look like. I’m working as much as can without wearing myself out but all I think about is when it’ll be our time. It’s funny (not really) but I’ve been told that if this the path I’m walking and being guided down then maybe God is saying I don’t deserve to be a mother. I think that’s rude and harsh but that’s her opinion so I’m deciding to leave that there.We’ll start the IVF process at the very beginning of spring after the holidays. I’m looking forward to continuing fighting and going through hell and back.

For now, it’s ovulation kits, timed intercourse, and trying some wives tales on how to get pregnant.

Until Next Time

xoxo

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That moment you realize no one believes you or your disease

I came to the realization that there are doctors, more specifically those who don’t fully understand what endometriosis is, and therefore think I’m faking my pain. It all started last Saturday at Kettering. I was in the ER for excruciating back and pelvic pain. I get back to a room where I wasn’t given an IV or anything. After a few minutes a lovely young lady walks in. I see she has a notepad and is in scrubs. So basically she’s a student learning for this shift. She sat down and asked the usual questions : why are you here? where is your pain? what has caused this pain? can you explain in more detail what endometriosis is? have you had surgery in the past? Tell me more about your surgeries. And this goes on and on and on and on because so many nurses have never heard of the term endometriosis before they encountered me. After sitting the room for over an hour, I’ve asked for water because I’m getting quite parched, they ask me to do a pee test. Now if I hadn’t seen what I did when I walked in maybe I wouldn’t be second guessing the reasoning  behind it all. And when the nurse came back into the room and said my sample was fine they just wanted me to make sure there wasn’t anything in my system. After that it was like here’s an anti-nausea pill and a shot of morphine and you get to go home now.

Here’s why I’m complaining. When a doctor can’t “see” pain it can be very hard to diagnose. But I feel like a lot of the time when things get too hard or their priorities shift they’re just like this girl needs to go there is nothing we can do for her. So now we are back at square one. I have an OBGYN appointment tuesday. As you can tell its 3am. I’m in more pain than you can imagine and the pain in my lower back is starting to spasm.

Until we have a day where information about endometriosis comes out and there is a cure or even a way to detect it, this is how endometriosis will continually be treated.

Until Next Time

xoxo

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My Mom Told Me to Stay off Facebook but…

Welcome to another late night post! The title of this blog is dedicated to my mommy. She saw that I got offended by a post going around social media. For those that haven’t seen the post it is an ultrasound of twins. People are posting that they’re pregnant only for the end of the caption to say we just wanted to say congrats to whomever is having these babies. It had been about the tenth time I saw the post and out of frustration I said it is really insensitive to post fake pregnancy announcements. Ya know, like the ones where everyone says they’re pregnant on April Fools Day, only for it to be a joke. Now after that I got feedback about my post, specifically from mommy. She said right now I’m too sensitive to be seeing things related to pregnancy so I should probably should stay away from social media. BUT we all know I have to play devil’s advocate here and now that I’m an adult I can (sometimes) go against what my mom says to do. (Although I could fail miserably while not taking her advice in the first place lol) She just understands what I’m going through, the serious amount of medication my body has undertaken over the last 18 months and the fact that it’s only going to get worse before it gets better. Anyway, I got some criticism saying that if we can’t find humor in some things then we’ll never be able to laugh at anything. So there are mixed reviews and my mom is just trying to protect me from getting my feelings hurt unintentionally by what one person posts. To be fair she is right. I’ve never experience a level of sensitivity like this. And for those who know me know I’ve always been a sensitive person but I feel like my emotions are a roller coaster. Not all days, but some days. There are days when I cry asking the universe why I’m not good enough for a baby. There are days when I’m angry or frustrated that I can’t get pregnant after 9 months of marriage. Then I just sit and wonder ‘why me’? I wonder if there is something I did in a past life to have to go through this now. Maybe it’s to make me appreciate the journey we are going on. AND speaking of journey’s, this Wednesday at 3pm I will be going to our IVF specialist for my Lupron shot! I have waited very anxiously to see what was going to happen. I’m so thankful for the nurses and Dr. Karnitis for doing everything they can to help us. From answering all my phone calls, voicemails, and seeing me when things seem to be a little less than urgent. I am blessed to have such an amazing support staff and although this shot is going to burn like hell it’s the very first step to take to get to IVF. This road is going to be long, expensive, and worth.every.penny. The day I get to create a life inside and hold my little baby Young for the first time will be amazing. I don’t even have words to describe that feeling now. All I can say is that feeling is a yearning. A yearning for someone I already know I love unconditionally. I have a yearning to hold them close to my skin, smell their sweet baby smell, all while delicately kissing each part of their face. Trying to become a mother is full of overwhelming, heartbreaking, hopelessness. But for us we can’t keep silent, even if people don’t understand. My goal is to just educate one person on how endometriosis can severely change the life of a young woman. So I’m sorry mom but I won’t be staying off Facebook because a message needs spread around the globe that women need more affordable healthcare for reproductive health. Infertility needs to be considered as a general service, instead of a specialty service that we no option but to pay out of pocket for. Infertility needs to be brought up because there are also women who can’t afford to seek treatment, therefore feeling lost. If I lose friends or lose supporters along the way through this, that’s on them. I’m on a mission and I Continue reading “My Mom Told Me to Stay off Facebook but…”

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Through the looking glass…

Have you seen the movie Alice Through the Looking Glass? Ya, I haven’t either. LOL But what I can gather from the title of the film is that Alice is going back to Wonderland to help the Mad Hatter. “Through the Looking Glass”, to me, is portrayed as looking at things or people from your own eyes. Have you ever just looked at someone and caught them at a very raw and vulnerable moment? To me, that is a through the looking glass moment (Now I could be totally wrong on how I’m using this phrase so please feel free to correct me if I’m wrong). This very thing just happened before going to sleep. I was going back into the living room to write and forgot I left the surface in our bedroom. I was being really quiet and I went in our bedroom to retrieve the surface but I see Russell eyes close, fingers laced together, praying. I can’t tell you what he’s praying for because he wasn’t saying anything out loud. But what I can tell you is I know he prays for me. He prays for our marriage, for our friendship, for our life together, for us to continually be as happy as we can be. For a baby. I know he prays for me to have peace because he knows there are plenty of times when I want to cave and just cry. There are moments when I’ve told him I don’t know how much more I can take. But looking at him in that moment was all the strength I need to keep pushing forward. Seeing him sending out positive vibes into the universe and praying for us to have our miracle baby, makes my heart so full. Knowing that this man is asking, begging, pleading for this month to be different gives me hope. He gives me the drive I need to keep going because there are so many days when emotionally I am not okay. I can’t tell you enough how much having him by my side has put many difficult and unexpected moments into perspective. The times when I’d ask “why?” or “when is it going to be our time?” or ” am I worthy enough to be a mother?” or ” am I being punished for something I’ve done?”. These questions are hard for anyone to answer let alone your spouse. The fear. The doubt that creeps in. All the negative emotions and thoughts that creep in every now and then are why I need him by my side. Seeing him take the time out of his day, even just for a moment to pray for us…. there are no words to describe that sight and feeling.

Going through infertility changes a woman…I’ve said this a million times before and I’ll keep saying that infertility changes everything about you. Infertility changes the way a woman looks at another with children, it can change the dynamic of a relationship, it can ruin friendships. Infertility has so many dark moments that seeing moments like Russell praying brings light into a very dark room. If there is one thing infertility has done it has brought us closer together. I feel like Russell and I are stronger and more connected than ever. I am glad I had this through the looking glass moment of watching him pray.

Keep stopping by for more updates on whats to come on your journey towards Baby Y!

Until Next Time

xoxo

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Plans That Do Not Go According to Plan

Do you ever just map out how your life or something really important in your life is going to go and then get really disappointed when things just don’t work out? Well that’s me; sting here at 1am with some very intense pain in my lower back and lower abdomen. I can never sleep so why not write a bit and try to calm down a bit to see if I can sleep? At least its thunderstorming so I can listen to that and be in peace.

Over the last year and half I’ve had plans of how everything was going to go. After surgery one in February 2016 I had a goal that I was going to get healthy and the endometriosis wouldn’t grow back (had I known then what I know now I would have just discarded all my plans). But as we all know March comes and so does surgery number 2. After March I decided I wasn’t going to focus on the negative and see how this “experience” would help me grow emotionally, mentally and physically. Well that didn’t work because I became very bitter and angry. Angry at the universe for giving me a disease that has no cure, no medication to control it and no way of knowing how bad it really its or how much of it has grown back without surgery. I cut myself off from my friends and even my family because all I wanted to do was be alone. I wanted to sit and think and really open my soul up to the universe and just try to figure out how to get out of the rut I was in. So I focused on our wedding, which was the best distraction I could have asked for. Planning our wedding was the most fun I’ve ever had! When August rolled around I had so much going on, I was finishing my year at Miss Captivating, in the final 8 weeks until we got married and then surgery 3 was scheduled unexpectedly. By this point I’d gained 25 pounds and just didn’t feel like myself. I had given up on looking good for the pageant because at that point there was no hiding the weight gain but I wanted to be present for that event and kind of shut my brain off that weekend. After surgery 3 we were in the clear (or so I thought). The final stages of putting our wedding together were going perfectly. Everything had been done and there were just a few last minute things to get for our reception. And the rest of the year went so well. We had consulted with my OB/GYN but for 3 months nothing. As newlyweds I knew that trying wasn’t going to be easy. Then out of nowhere surgery 4. The big one. The one that for me was the hardest. I think my body was in so much shock from the previous surgeries that it really had no recovery time; in 12 months I’d had 4 surgeries. In January I got really discouraged and we kept trying until this spring when we went to see Dr. K. at KHN. Ever since we’ve been going through this regimen and I’m hoping it works.

Last month was a true example of how things didn’t go according to plan. Last month I had my first round of Clomid, followed by a trigger shot and timed intercourse. And let me tell you that’s really awkward to hand your husband a schedule and say these are the days we need to try for a baby. We did exactly what the doctor and the morning I took a test I couldn’t look at it. I peed on the stick like you always do and then put it in the box. When Russell and I looked at the results, which was a negative, I broke. I never knew I wanted something so badly until that moment. At that moment I went back to bed and just cried. I realized then that this entire process is about not having anything go according to plan. I have to give up all my expectations because if I don’t I will continually be let down. This entire time I’ve had a plan but at some point I have to give everything I have to the universe and say ” Okay. I give my everything to you. You will bless us with a baby when you feel the time is right.” I ask the Goddess of Fertility for her help because I know she is looking over us.

Throughout this process I’ve had to learn how to love and let go. Let go of the baggage I’ve been carrying around. Let go of the negativity. Let go of this idea that having a baby later in life is a bad thing. Let go of the judgments I’ve placed upon myself. Let go of the what if’s. There are so many things that don’t go accordingly to plan but if having a baby means not sticking to any agenda, I’ll take it. We’re patiently waiting for our sweet bun to come to us. Until then, I’ll just keep writing and hoping we are making progress.

xoxo

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Mothers Day 2017

Please stop asking if I’ll be okay this Mother’s Day. Yes I understand the significance of the day and how I’m struggling to conceive myself. However, I am still able to spend mother’s day with my three awesome doggies and husband… after all I did become a fur-mama almost 9 years ago when I surprised Russell with Lena!!! Not to mention I get to celebrate my WONDERFUL, AMAZING, puts-up with all my shenanigans mother!

For me mother’s day isn’t about dwelling on what I don’t have but rather being thankful for what I do have. I have an awesome mom (and step-mom) that I am blessed to walk through life with. I think of the numerous times a day I call her to tell her the most random things. LOL. But for me Mother’s Day is about celebrating all mothers, including those who may not have children on earth but have children watching over them. You, sweet sister are still a mother, no matter what anyone else says. I believe this holiday will afford you the blessings and light you may have been looking for.

While our journey hasn’t been easy or as long as some other people I know, I do know that we are on the right track. Yes, I do have down days where I can’t seem to think my way out of what is going on; so I sit and let my emotions surround me and with every breath I take I feel how deeply my emotions are effecting me. Once some time has passed, I am usually able to get through anything. Which is why I don’t want anyone else asking if I’m going to be okay on Sunday. I want people to celebrate the amounts of achievements we’ve had this year. I want to celebrate being a strong woman, one in which is putting her body through the ringer in order to conceive a baby. I want people to understand that I have stage four endometriosis but that I won’t let it define me.

Now, please understand that I feel for any woman who has lost a child. I can’t imagine what that feels like. My hope for you this Mother’s Day is to remember them how they were, what they would look like and what their voice would sound like if they were to call you ‘Mom’. I know it sounds painful but in sad moments we can find joy. So find joy on Mother’s Day. Smile. Laugh. Cry happy tears. Be with your loved ones and know that they understand what you are going through. Life is forever changed when we lose someone we love. Milestone holidays become big days and days we often run from. Let’s not run from our fears but instead face them with every fiber of our being. Because at the end of the day in order to get passed a challenge we must go through it. We can not go through a challenge if we are not ready. Each woman is going to be different. Each woman may not agree with what I’ve said.

I don’t want to be asked if I’ll be okay for major holidays just because others have children and I don’t (right now). Mother’s Day is about celebration for me; fun memories; loving times. I hope when the day arises and you may not be feeling like getting out of bed, you remember the purpose of your being; to stay strong even when you feel like giving up.

Until Next Time,

xoxox

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Sweet Saturdays

So I haven’t had a Saturday off since my last surgery. I can tell you it feels weird and even when I had more corporate job I worked in the morning on Saturdays. (I always have Sundays off because I truly believe Sundays aren’t meant to be worked. And I sure love a good football or baseball game on Sunday!)

So we haven’t been up to much since my last post a few weeks ago. I’m stilling our IVF doctor and just completed my first round of Clomid! I can say that the hot flashes are the worst. And I can’t tell which ones were worse… the ones form Lupron or the ones from Clomid. I didn’t have many side effects, except for the occasional headache and I was able to manage those just fine. I had no nausea or vomitting like the directions said I could so that’s a good thing. I did feel a throbbing in my lower right side which the doc said would be normal as my eggs are hopefully getting bigger! AND we had 4 eggs when we started so hopefully on Tuesday when I go for my next ultrasound we will see some pretty good looking eggs.

I can say when all this started I never realized how difficult it would be. I just thought I would have surgery to treat the endometriosis and be on my merry way. I never realized what this disease could do to a person both mentally and physically. I guess you just never know what you are able to withstand until you are faced with adversity. I can say that our families and friends have been really supportive and loving during this time. As I mentioned in a post earlier this week, we do have a plan in place but I won’t be as open about our plan as everything else. Our plan is something we decided together and we’d like to keep it private until we are able to get pregnant.

Speaking of getting pregnant, did you know Russell told me he really wants a January baby?! I had no idea he wanted a winter baby until about a month ago when we politely asked if we could have one around his birthday…more specifically he said he wanted one with his Zodiac sign! I couldn’t help but laugh because I said you can’t request what month your baby is born in. He said he could and is adamant that we’ll have more than one and one will be a January baby. This just goes to show you that even throughout all this stress and heartache does come laughter, which is the best kind of medicine!

I hope you all have a wonderful Easter weekend and are enjoying this weather!

Until Next Time,

xoxo

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Endometriosis Awareness Month

All month long I’ve tried to think of what to write. For some reason the words are there but I can’t seem to formulate the right sentences to create a coherent blog post. Here’s my best attempt to put everything into words 🙂

March is endometriosis awareness month. I’ve been reading stories all month from women sharing their stories, their fears, their goals, and what they hope they can accomplish by sharing what they’ve been through. The stories I’ve read all vary from women who have just been diagnosed to women who have known they’ve had this disease for a few years or more. Then I read one where a husband shared his point of view on what it’s like to take care of someone with endo. The story was awe inspiring. For me it touched a special place in my heart. It made me feel vulnerable in a way that I started crying. His words were so sweet and kind. He was gentle when he described the way he cares for his wife daily. I think that’s something that most people who don’t have this disease realize. When a man decides to marry a woman with this disease, he is marrying someone who is going to be tired, sick, and have flare up’s so bad nothing but an ER visit can take away the pain. Naturally, when I was reading this blog post I thought of Russell. I think of every day when I have to tell him my back hurts, or the cramps are more than cramps. Ironically its been 365 days since my 2nd surgery… ya know the one where they had no choice but to take out my left tube and ovary. It was that hospital stay that I asked him “Are you sure you want to marry me? What if I can’t give you children?” It was in that moment of imperfection, laying in a hospital bed, so drugged and sick that he told me he loves me for everything I am and if we can’t have kids then we have each other. Ladies, the one thing I know about Russell is how much he wants a family. His desire to have a family is strong. When a man marries a woman with endometriosis he marries the idea that children may not come. I thank the universe for Russell every day. My husband is an endo husband. He takes care of me. He tries to make my pain go away and comfort me when I’m at my worst. If you or someone you know has an endo husband, hug them tight. They are hard people to find. They are like finding a needle in a haystack. Endometriosis can put stress on a couple. It can make you both for guilty. Us women feel guilty for our spouses because we are keeping them from a healthier person. At least that’s one of my biggest guilty feelings. I tell Russell all the time that he could have been with anyone else. The guilt of being sick all the time creeps in and makes me feel awful. I think that’s why I needed to read a story about a couple going through endometriosis, and the article being written by the husband was on point. He committed to being the best endo-husband he could be. He told the readers of how many heating pads they have and how it doesn’t take him long to heat them up for his wife when she has a flare up. He also talked about how he knows when to step in and tell his wife to rest and when he knows she can push herself. An endo-husband is a caretaker and without them us wives would be lost.

I want to thank my endo-husband. Thank you for baring with me during the last year. I know four surgeries was tough. Four surgeries were stressful emotionally, physically draining and mentally challenging. Russell has been there for the darkest days of my existence. He has seen my biggest fears with endometriosis. He attends IVF appointments to educate himself further. I also am thankful for my endo-husband because every day he tells me we are going to be parents and he’ll see me grow through motherhood. I’m thankful every second of the day for my awesome husband. I am thankful for the support, advice and love he has given to me in the last year.

Having endometriosis is debilitating, it’s frustrating but in the end endo is apart of me. I have learned and grown so much this last year and I hope that if you are following this journey I have taught you a little something about endometriosis that you didn’t know before.

Happy Endometriosis Awareness month March!!!!

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How are you feeling?

Do you ever just have something happen to you and you look back and see what you could have done differently to prevent it?

Well that’s been me for the last few days. To say I’m in some pain would be an understatement. I was finally able to change my bandages and look at my wounds for the first time. It’s definitely not what I thought it was going to look like. I thought since they went in laparoscopically my incisions wouldn’t be so bad, but I was wrong. Two of my incisions are quite large and my belly button has two more incisions with another small incision close to my left hip. The pain is constantly throbbing and my back almost always hurts.

Here is what they did to my body: Going into surgery I knew that my uterus was going to be reconstructed because it was somewhat damaged. However, my OB found that both my ovaries were conjoined, which were attached to my uterus, and my uterus was attached to my bowels. So basically all my parts were frozen together, giving me all these crazy symptoms when I was on my normal period. During surgery my left ovary and fallopian tube were so enveloped in scar tissue that they were damaged beyond repair. Once they took out my left ovary and tube it was time to take care of my right one. My right one wasn’t perfect, it had some damage that they were able to fix but in the end I am left with half of my right ovary and a fully functioning tube. (YAY) Of course after that was done the rest of the endometriosis was removed. From what I understand there was a lot of damage done an it was very hard to fix (surgery was 4 hours)but they got the job done which is all I wanted.

The main question I keep getting asked is this: How are you feeling? Well honestly, I have no idea. I’m out of work for two weeks if not three, I can’t do much of anything because of the amount of pain I’m in, and we only have a 25% chance of conceiving a baby the natural way. So the answer to “how are you doing?” is not so great. I feel like I have to say I’m fine or that things are going well because people don’t want to hear about the awful stress my body and my emotions are going through. There are plenty of times in the hospital that I cried because I don’t have all my lady parts. I cried for Russell because I feel like he is marrying someone he is always going to have care of. I wonder if I would have taken better care of myself if this could have been avoided. I wonder how I got so lucky by having someone love me as unconditionally as Russell. He is always willing to take care of me even on days when he isn’t feeling well or he’s having an off day. Sometimes I feel like he deserves to be with someone who is healthy and can do everything he wants to do. But I’ve come to realize that’s not life. Life is growing old with someone, taking care of them because you love them, being selfless in a time when you probably deserve to be selfish.

Finding out that I have stage 5 (extensive) endometriosis it felt like my world was falling apart. I felt like I was being kicked in the gut. Each day brings a new struggle. Each day a new emotion arises that I have to face head on. Today I am feeling overly emotional because I want a baby. I want to give Russell a family. I want to feel what it’s like to give birth to a baby. I want to be up all night feeding and changing diapers. But what people don’t understand is that this disease can rip those hopes and dreams away from a woman in a heartbeat. I want to be one the women who can beat this. I wan to be able to say I have “x” amount of children. It may take a while to get there but I have to keep faith that everything is going to work out. My plan for life has already been mapped and I just have to keep following it.

xoxo