Accept it…

Accept it…and then challenge it! About 5 months ago I said enough is enough.   I was miserable.     How can you be miserable with a beautiful baby in your arms?  Well… part of it is you keep saying to yourself, “what the hell is wrong with me; I have everything I’ve ever dreamed […]

Why am I begging? 

If you follow me on Facebook or basically any other social media I have probably been driving you nuts with my post lately.  I’d apologize but I can’t because it is just that important.  My Husband and I have been fighting for over a year now for Congress to pass legislation to allow the VA to provide IVF coverage to our wounded Veterans.  I know other couples that have been fighting for over 6 years for the same thing.  Year after year this gets put on the back burner.  Year after year it is voted down or taken out.  Every precious year during our child bearing years is quickly passing us by, while we wait for Congress to decide how they “feel” about IVF and other fertility treatments.

Congress- WE DO NOT HAVE TIME!  44% of Maryland’s Post 911 Veterans are in their prime child bearing years.  When you hit around the age of 35 fertility discussions start to become different.  My Husband spent 2.5 years at Walter Reed recovering from significant injuries that he sustained in Afghanistan during his first deployment in our Army’s Infantry.  Kevin lost his leg and suffered extensive injuries to the rest of his body.  He also lost a testicle that resulted in a significant decrease in fertility.  Every test and doctor we have seen has said the same painful words, we will never have children on our own.  We were told that we would be covered through the DOD if we did IVF while he was active duty.  A perfect time to bring a child into the world… between surgeries and a very unstable situation… NOT! We made the responsible decision to hold off on having children until our life settled and we were ready. Since we waited, we lost coverage for IVF treatments that we needed.  The VA cannot provide IVF treatments to any Veterans, including those who need it because of a war related injuries.  After Kevin retired the VA ran every test, looking for options because they desperately wanted to help us.  Unfortunately they had to tell us that they were unable to help.  Why? Because our government placed a ban that prohibits the VA from providing the treatments.  The funny part is, the DOD is able provide it.  Why is there a difference between the two?

When we met with members of Congress we were hit with some pro-life issues.  Apparently pro-life is not an issue for DOD even though the IVF is provided the exact same way.  IVF is as pro-life as you get.  We are starting life, we are trying to have a family, not end it.  I’m not sure why our veterans are being hit with these questions when all they are asking is to start a family and to have a more normal life.   It is unfair and unethical to make them feel anything other than supported when trying to pursue their dream of having a family!

Our life will never be normal because of war.  Parts of my husbands body are somewhere in Afghanistan and the 2.5 years he spent recovering he will never be able to get back.  Does he regret it… no, he doesn’t.  His Mom had to live with him for about 2 years to care for him through over 30 surgeries.  Now he is medically retired.  He is going to school for his Bachelors degree.  He is ready to be a Dad.  His Mom, who had to wonder if her son would survive, is ready to hold his baby-her Grandbaby.  This is what normal looks like for so many.  All we are asking is for a piece of normal, to be able to be parents.

The reason I am pushing so hard for support now is because Congress will soon be going on break.  If this is not voted on as a yes, more years will continue to pass and more families will be faced with trying to figure out how to have a family.  Like I said before, many of these soldiers are in their child bearing years now, they do not have time for this to take longer! Our wounded service members deserve better.  The ultimate goal of recovery after a war injury is to go on with life as normal as possible, to make the person whole again.  By passing these bills we are helping to make these men and women who already gave so much, whole again.

If you have children, look at them and ask yourself what you would do to bring them into this world if you had to do it all over again.  That is all we are doing.  Our baby is not due until August, but we know the love for her is immeasurable because we have and will do anything to bring her to us.  We will also do anything we have to make sure other people in our situation do not have to feel the way our Government has made us feel.

Please help us by sharing with Congress your thoughts.  We welcome you to use our story.  There’s over 2000 known cases of Veterans who now face infertility because of war injuries. Let’s stand up for these people and help change their lives.  So often we hear “thank you for your service” and we know the people mean well but a true thank you is to help fight for these men and women.  The link I am going to post is a quick and easy to write your representatives requesting that they support these bills.  You do not even have to look up your representatives, they do it for you!  You don’t even have a to type the letter, it is done for you (although you are welcome to add and change things).  You simply put your name and address and it is done!  Something so simple could change the lives of so many and would truly be a meaningful “thank you for your service” for so many!

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Click here to let your voice be heard!

Transfer Day! Officially PUPO!

We are officially PUPO!  This typically stands for “Pregnant Until Proven Otherwise” in the infertility world.  However, I decided to change it to “Pregnant Unless Proven Otherwise”.  The word “until” seems too negative to me; like eventually I will get the phone call that we are not pregnant.  I like the word “unless” much more.  To me this word means that it may not happen.  That I may not get the phone call that I am not pregnant.  Unless means that I have every reason to believe that I will get the positive phone call; and if we do not get that phone call, we will cross that bridge at that time.

This morning we watched our embryo get placed back into its home.  It is now in the blastocyst stage.  Our little embryo is even starting to hatch!  Before I started this journey, I did not realize that humans do

hatch!  This has to happen in order for it to implant into the uterus lining. In two weeks, we will get blood work done.  This will help us if our embryo has survived.

We appreciate all the thoughts and prayers during this time!  The next two weeks will be difficult to get through but we have hope!  Kevin and I choose to be public about this journey in an effort to educate as many people as we can about something that impacts 1 out of 8 couples.  In someways being public is very difficult.  I am still sad sometimes that we will not get the cute surprise pregnancy announcement like most people do.  I also know that if we receive not so happy news in two weeks, it will be difficult to go through that publicly. However, we decided that the impact we can hopefully make is worth it.  We also hope that anyone going through this knows they are not alone.  We want to break the silence that so many feel they must live in while suffering from infertility.  Infertility is a disease that is represented in both men and women equally.  1 out of 8 couples suffer with it.  Our story is just a glimpse into this world and we hope it brings the issues to light.

We will keep everyone updated!  Keep the prayers coming for Baby Jaye and pray for a BFP (BIG FAT POSITIVE)!

This is an actual picture of our embryo!  This picture was taken today; before it was transferred back! It is starting to hatch as you can see on the left side of the picture.

This is an actual picture of our embryo! This picture was taken today; before it was transferred back! It is starting to hatch as you can see on the left side of the picture.

Emotions are high, hopes are higher!

Yesterday was our first appointment with Shady Grove Fertility.   I spent hours researching infertility and some options we may or may not have.  I thought that would help me prepare for everything the doctor was going to say.  It didn’t.  I wasn’t prepared.  I felt like a deer in headlights.  I have no idea what all of the acronyms they throw out mean and I found myself frustrated.  We had to fill out a ton of paper work after the appointment.  It was like purchasing a house… with much tougher questions.  First, we had to decide if we would want our remaining embryos frozen after our first transfer.  Sure…  I think.

Then, there was this question…

“What do you want us to do with you embryos if something happens to two both of you?”

WHAT? I didn’t prepare for that question. It actually never crossed my mind that it would even be asked.   We will have frozen embryos just waiting for us to use them.  If one of us passes away, the embryos’ still belong to the living person.   This just makes me feel weird; I am making plans for my children before they are even conceived.  I don’t know how I feel about it.  I am trying to understand that it is okay to do this.  I am thanking God for giving us such brilliant people who will make it possible for us to have a family.

Then the question, “if you do not want them anymore can we do research on them or if they die what do you want us to do them the remaining tissue?”  Um… okay, it will help other people out right?

Who has to make decisions like this?  Why do we have to?  Why can’t we be like other people who can get pregnant naturally? If he wasn’t injured, this wouldn’t have been an issue.  I hate these questions and I feel bad for feeling them but… I feel them.  Kevin does not deserve to feel like this is his fault, because it is not his fault in the least bit.  I’m very much in love with him and I wouldn’t change a thing.  I know he feels guilty sometimes, but he shouldn’t.  If all of these things didn’t happen, I’m not sure that we would have been brought together.  So I will take the good, the bad, and the ugly because I found true honest love.

Then I think about all the exciting parts of the beginning of a pregnancy and it makes me a little bit sad.  Announcing to your husband that you are pregnant and the excited look on his face, what beats that (besides obviously his face when our child is brought into this world…man I cannot wait for that moment)?  Telling your parents that they are going to be Grandparents, telling your siblings they will be Aunts and Uncles, has to be an amazing feeling.  We won’t get that, people will know we are trying to get pregnant because I will be giving myself shots and going to never-ending doctor’s appointments.  It doesn’t seem like something that will be easy to hide from everyone.  There will be no surprise.   I feel like during the two-week wait I am going to be stared at day after day, everyone will be waiting to see if it worked.  Then we will sit in a doctor’s office and they will tell us if it did work.  If it didn’t work, what do I say? What do I do?  If it did work, it would change everything for us.  More than likely, it will work and all will go well.  I’m trying to stay out of the world of “what ifs”, that world is terrifying and a waste of my time, but sometimes we all visit that evil world.

I know this will get easier to understand and deal with over time.  I’m so thankful that we decided to look into this now; so we have plenty of time to get comfortable and knowledgeable before the actual IVF procedure starts.  It is just hard right now.  Sitting in the doctor’s appointment, hearing things I did not understand, and thinking how I am going to get all of this straight is very overwhelming.  I’ll be okay, we will be okay, and our future children will be okay; I just need to work through the confusion.

I’m excited to start thinking about the real possibility of Kevin and I having a family.  I know he will make an amazing Dad.  I cannot wait to look at them and hopefully see his smile, eyes, and overall love for life in them.  I don’t mean to sound “woe is me” about this subject, nor do I want pity.  I know thousands of people go through this all of the time.  Just right now, in this moment, I am tired, confused, frustrated, excited, and scared.  Most of all, I am thankful, so incredibly thankful, for doctors, nurses, science, and God for giving us the opportunity to raise a family of our own.  Kevin and I are strong, we fought through everything that was supposed to bring us down.  I know we will get through this too.  I just cannot wait for the day when I can spill off all the information about this process without being confused or mixing up terms, or trying to figure out when I am supposed to take what test and where.  It is a whole new world to us, I’m embracing it with open arms, and with a side of anxiety.

Every season brings new beginnings and new life.

Every season brings new beginnings and new life.

“I’m so OCD”… no seriously

The definition of OCD (Obsessive Compulsive Disorder) is the presence of unwanted thoughts leading to excessive compulsions and it is pure hell!  I was diagnosed when I was 10 years with Anxiety/OCD.  I never understood why until probably just this year. I knew I was easily upset and that things would make me nervous and angry, but did not really realize that it was not typical.  That is 17 years of not understanding why my brain was torturing me.  I always thought having OCD meant you had to have everything neat and tidy.  I knew that wasn’t me because most of the time I feel like everything is a disaster. Growing up I never kept my room cleaned up perfectly. I think a lot of people have this misconception. Someone with true OCD does may want their things in a particular way, but not jut because it looks nice or fits nice there, they take it to another level. It tortures them until whatever needs to be changed, is changed. The behavior they demonstrate is a result of whatever they are obesessing about.
Mental illnesses are not well understood in our society and they often carry sigma.  People often fear sharing that they have a mental illness because of judgement and shame.  I like to see it more as a “quirk”, it is something I struggle with at times, but it does not define me.  What defines me is that, I am a Daughter, Sister, fiancée, Teacher, Friend and so much more. I am not OCD.

Here is some background information about when this all started for me:

On day in the summer of 1998, my sister and I were watching TV downstairs. I remember hearing thunder and running upstairs in a panic. My parents were getting used to my storm freak outs so they were trying to help me through it.  We turned on the TV to check the weather, the power went off.  Then we opened the blinds to look outside to prove it was just a regular storm-the tree in our front yard was bent so hard that it was touching the ground. That is when we realized this wasn’t your typical storm and went downstairs.  Later we found out it was a tornado. I think the tornado may have registered at a F1.  The damage was minor and mostly consisted of down trees and derby thrown around.  We were without power for several days.  It completely rattled me.  I started to not want to go outside anymore.  Anytime there was a storm I was a complete wreck.  I remember my Mom buying me those fuzzy posters to color during storms because it kept my mind busy and at ease, at least a little bit. One of my Dad’s co-workers had an old book about the weather and they gave it to me to read.  I read it and I learned about storms, it helped me significantly.

I also developed a terrible fear of dogs, to the point that leaving my parents front porch was not an option because a stray dog might get me.  I had grown up with a large German Shepard/Lab mix.  She was sweet and gentle.  I wasn’t afraid of her but she passed soon after my anxiety had ramped up.  I remember not wanting to go to family members and friend’s houses because their dog might “eat” me.  Then, my parents bought Amy (my Sister) and I a puppy for Christmas.  A puppy wasn’t scary to me because they were so small and helpless.  We raised her and I swear to
this day that a lot of fear was taken away by her.  If a storm was coming she would lay with me until it passed.  She helped me over my fear of dogs by showing me how gentle they really can be.  Immersion therapy at its best.

In 1998 I lost my Grandmother.  She was in her early 70’s and she was the only Grandparent I had left.  My Mom’s parents passed away by the time she was 5.  My Dad’s father passed when I was 2 years old.  My sister and I were her only Granddaughters at the time.  My Grandma came to our Ballet recitals,stayed with me when my sister was born, came to school to volunteer and read to my class.  She was an amazing woman and I wish I had more time with her.  My Grandma fought Pulmonary Fibrous.  Her lungs were hardening everyday. She found out she had the disease the day that her husband, my Grandpa, died.  She lived 8 years with it, which is longer than most people do.  The doctors said that had my Grandpa not died when he did, she would have died sooner.  My Grandpa smoked in the house and it impacted her health greatly.  The night before my Grandma died we went to visit her at my Aunt’s house.  She was in a medically induced coma.   She was just laying there in a hospital bed in a room in their house.  I remember sitting in the room with my family, my Dad talking to her, and be given some jewelry that she apparently said she wanted my sister and I to have, and I remember getting slippers for some reason.  When we were leaving my Aunt’s house I remember sitting in the car crying hysterically.  I knew that was it, I was only 10, but I knew.  The next morning we were supposed to go to school.  When I woke up I noticed it was late and my alarm hadn’t gone off.  I knew she had passed.  My parents had turned off our alarms to let us sleep… a few more minutes of some normality.  We packed up our stuff and headed to Pittsburgh, where we planned and attended her funeral. In about a week we were home and back to “normal”.  My Grandma was an amazing person who I love very much.  Although she had passed by the time I was 18, she had set aside a piece of jewelry for my Aunt to give me on my 18th birthday.  Nothing as ever meant so much to me.

I cannot remember the exact timing of everything else but around this time my Mom got very sick.   The doctors could not figure out what was wrong for what felt like eternity.  She was in horrible pain all of the time and was just very sick.  I remember one night in particular that I thought I was going to lose my Mom because it seemed like her body was failing her.  I thought I was going to have to experience what she did with losing your parents at a young age.  It was terrifying. I specifically remember the terror, my sister was not much older than my mom was when my Mom’s parents died.  I was convinced in a way that it was our “fate”, and it was going to happen to us too.  Needless to say, the doctors eventually pin pointed the problem and were able to help.  During the time that she was sick, my Dad obviously was the one enforcing rules.  My Mom was always against us watching The Simpsons, but since she was sick and Dad was in charge so we got to watch it.  It ended up being something we watched as a family after she got better!  Thanks Dad! haha!

My worst fears have changed from storms and dogs to losing someone I love.   I worry at probably 10-15 times a day that something bad will happen to a loved one, each and everyday.  I imagine that I was probably born with anxiety.  However, the obsessive behaviors started around the same time as those events.   My life experiences have shaped my anxiety into what it has become.  Now, don’t get me wrong…I had an amazing childhood.  I was raised by two of the most loving parents. This just goes to show that no matter where you come from you do not get to escape mental illnesses.

My obsessions are always linked to fear of someone getting hurt.  My compulsions are always linked to an attempt to make sure nothing happens to that person.  It is like my mind is playing with me, trying to make me feel that I can control keeping them alive if I just do whatever is in my brain.  My compulsions are typically a random bunch of things.  I HATE odd numbers.  If I turn my radio volume up and it lands on an odd number I have to change it.  If I do not change it a family member may die in a car accident.  Sometimes it is that I must have the stupid dial on the dryer exactly lined up or I am screwed.  My compulsions sometimes consist of me seeing something on a fridge but not really reading it, but then I am forced to go back and read it in its entirety or someone has a heart attack today.   It is so frustrating, heart-breaking, and a waste of my time..  I don’t want to read what is on the fridge, I don’t care if the dial is lined up perfectly on the dryer, and numbers are just numbers.  However, my brain won’t let it go.  I know it is not rational to believe that I can keep someone alive by performing these dumb rituals, but I am terrified of what would happen if just by chance they did get in a car accident.  I would never be able to function again because I would always think, well maybe I should have done that, even though sensible me knows that it is completely irrational.  I’ve told my family over and over again that it is really exhausting to keep them alive all the time!  I can laugh about the thoughts that come in my head afterwards, because I know they are irrational and no where in the realm of possible, however in the moment I cannot laugh because all I feel is fear.  Who in the world wants to think about people they love getting hurt?  I know I don’t!  I wish I could just cross that bridge if it comes instead of obsessing about it all of the time, but I do not get that luxury.  One time my counselor said that I should focus on being with them and happy memories… so much easier said that done.  Instead I think, what if this is the last time I see them, what if, what if…

Fear tries to run my life, but I always try to fight back.  If you could hear inside of my head at an airport you would wonder how in the world I ever get on an airplane. I do because I can’t let it win, I fight like crazy.  I think airplanes are fascinating machines.  However, I am terrified of dying, not because I don’t want to die (which I don’t, life is pretty awesome and the unknown of death is scary) but I am afraid of what would happen to the people I love if I did.  Would my sister be able to function?  Who would call my Mom everyday at 4?  Would someone else love Kevin like he deserves?  And the thought of my Dad crying makes me want to cry typing this.  I don’t ever want them to feel pain.  I felt like a selfish jerk when I finally decided to reach out and get help for this because I felt like I saying I was putting myself before them. It felt like I had stopped their cancer treatment to keep them alive.  It is that crazy talk again going on in my head… I wasn’t controlling keeping them alive or safe by doing the things I was, I was just falling victim to the anxiety.

When I was diagnosed at age 10, I was placed on medication. I saw a counselor and a psychologist.  As I got older and with little understand of what was going on in my head I stopped the medication and therapy.  I managed for a long time.  I had the obsessive thoughts of people getting hurt and I tried to control it and sometimes I could.  I basically just gave into the compulsions because they didn’t completely interfere with my life, they were just annoying and confusing.  Then I got married.  I was under “fight or flight” all of the time. I had stomach ulcers and bleeding and all kinds of issues.  I ended up on anxiety medications during this time.  When I left my ex-husband I stopped the medication and I was doing pretty well for about a year.  Then anxiety let me know that it never left, I just suppressed some of it, but it showed it’s stupid ugly face again.  I was crying a lot at night because I was so frustrated with myself for feeling anxious all of the time. I experienced many more funerals and watched people grieve loved ones.  I have a very bad habit of putting myself in someone else shoes and then I get in extreme distress.  If someone loses their Mom then I think of how hard it must be for them and then I think what if I lose my Mom?  Then it spirals out of control. I started to get angry with myself because I am very aware of how irrational my anxiety can be.  I was tired of feeling “crazy” for being worried all of the time.

I still struggle but I am aware of now. Sometimes I do not respond to people talking the first time they say something because my anxiety in my head was all I could focus on, it consumes me.  I sometimes get frustrated if someone talks to me while I was stressing out about something because it is interrupting my obsession/anxiety and I was trying to work through it.  I’ve snapped at people I love when this happens.  I struggle with noise, I hate anything loud, it just makes me feel nervous.  I hide from people in my room or in the bathroom sometimes, just because I need quiet for just a few minutes.  I have found my own ways to cope with the anxiety at times.  Sometimes I give myself a “timeout” if I feel like I am going over the top.  I research things that make me anxious such as airplanes, weather, etc.  This has helped me tremendously.  The more I understand something, the less I am afraid of it.  I have not conquered my fear of losing people I love, it still haunts me everyday but that is okay… I win more than I lose to anxiety! I 1,2,3 things when I am scared (read 1,2,3 go blog to understand this).  However, I think the biggest thing that has helped me is talking about it and accepting it.  I hid from this for a long time… 17 years! I was shameful, embarrassed, mad, frustrated, and basically any other emotion you could think of.  It is not fair that I have to take medication to keep my anxiety levels lower.  However, it is not fair for me to live in a state of panic 24/7 so I thank God for science to give me this relief so I can enjoy this beautiful life.  No one has a perfect brain and we all fight our own demons.  Be honest about them, most importantly to yourself, because with that comes the opportunity to live the life you deserve.

My Grandma & I

My Grandma & I