Showing posts with label trisomy. Show all posts
Showing posts with label trisomy. Show all posts

Saturday, March 15, 2008

All About Makily!


Things Makily likes (in no particular order):

TV, SpongeBob Squarepants, Nemo, Swings, being talked to, being sung to, cuddling, jumping in her Jumperoo (although we have to "adapt" it since she is such a big girl now), dancing (you hold her and dance), riding in her remote car, playing with her toys, all the Disney parks, swimming, watching TV upside down and looking at faces upside down (this makes her giggle like crazy), MUSIC, bath time, people with any kind of strange hairstyle, school, Mrs. Leslie and Mrs. Byrd, looking at herself in the mirror, being told how wonderful and beautiful she is, her sleeping bag, her obnoxious turtle and her "symphony" V-tech toy from Laura, her Daddy, watching other kids be naughty, Cops and Police chase shows (she always laughs when they crash), Nanny and Granny....and well okay Mommy :-)

Things Makily HATES:

Hats, things on her face, eating by mouth, laying on her tummy, TV commercials (she screams now when they come on), anything poked in her ears, blankets, shoes, having her teeth brushed, BRUSHING HER HAIR (I get the wrath of Hell every day for that one), water in her face, getting sleepy (she fights it), being put in her car seat, the sun in her eyes, being hot, EEG's and sleep studies.

Like I mentioned above Makily loves music, being sung to and dancing so much. I had her in the den the other night while I was blogging and she was playing. I put some music on and sang and danced like an idiot for her. She loved every minute of it so I decided I had to catch it on video. Makily LOVES my singing and dancing but it has to be INSANE and over the top so Sorry guys you only get to see my baby giggling and not my acting like an idiot for her.




Side note: The foster thing is taking FOREVER. We aren't getting anywhere fast. Our home study was reviewed by the agency and yet again they have more questions. We have answered HUNDREDS AND HUNDREDS of questions you wouldn't believe and I can't imagine what else they would possibly need to know about us. I have not received them yet but I know they are coming via email next week. We are very frustrated especially when they keep telling how bad they need homes like ours. They are desperate for newborn stay at home foster moms. Allen and I have decided to stop holding our breath and sitting by the phone waiting for it to happen. We are going to live our lives and when we get a call for our license then that's great. Will keep you updated.


Friday, November 11, 2005

The first week......

I woke up the next morning at about four am. My sister Elizabeth was laying on the sleeper sofa in the room with me half asleep. The TV was on, I started replaying the night before in my head. It had not all been an awful dream....this was real. My baby was not even 12 hours old and was 30 miles away from me.....and I had no clue how she was. I called my husband at home and he answered and sounded terribly tired. He had been at Shands till about 2am. I told him to go back to sleep, he was going to be coming back to see me at 9. My sister stirred and I asked her to help me get up to go to the bathroom. She did and I just kept crying and thanking her for being there. I am incredibly blessed to have such a wonderful supportive family. I took a shower and cried through most of it. I still can't believe this is happening.

We had the nurses put a no visitor sign on my door and I wouldn't take any phone calls except from immediate family. I couldn't talk to anyone. I was barely able to hold myself together and if I had to repeat what was happening to me over and over I don't know if I would have been able to keep it together. The thought of hearing one more person say "I'm sorry" was enough to make me hysterical.

I was so numb, sad and confused.

It's strange because I was trying not to let myself think of all the things that could be wrong with Makily....I mean I KNEW something was wrong BUT my mind wouldn't let me think of it.....I just shut down. I do believe that you have a defense mechanism in your brain that helps you shut these things out when your are dealing with too much at once.....never believed that until I had Makily.

Allen got there and Dr. Pierre came in soon after. I was happy to see her but apprehensive at the same time. I knew that SHE KNEW something was wrong.....she most likely knew what it was.....and honestly I didn't want to know. She was so caring and was patting my feet and leg as she was talking to me......this was comforting. She told me that the doctors at Shands thought Makily had Turners Syndrome. I didn't know what that was....she explained it to me. Basically Turners girls are short statured, may have scoliosis and growth issues and are infertile.....but cognitively they are usually "normal". I could handle that I thought, yes I was sad but I thought at least it's not too bad. She stressed they weren't sure what it was really and that Makily had blood drawn when she got to the NICU to test her chromosomes. She also explained Makily had Pierre Robin Sequence. It's an abnormally small chin/jaw, recessed tongue and cleft palate. I didn't notice her chin being small when I had held her the night before. I had been so out of it though.

Dr. Pierre left and I remember Allen pulling a Polaroid picture out and giving it to me. It was my daughter. I briefly looked at it and put it away. She looked awful. Tubes and wires everywhere...she was so pale, she honestly looked dead to me. My mom and dad came in and very soon after my Doctor came in. He asked me if I wanted to leave the hospital and I said yes. He was extremely nice to me. I was angry with him for ignoring me the day before and I am sure he was freaked out when he found out my baby was so sick. I had more things to worry about at the point than him. He said he would release me but I would have to have a two week post partum so he could make sure I was okay. That was fine.

We got checked out at about 11 am. They wheeled me out into the hall and I looked over and there standing in the hall was a Daddy holding his precious newborn in his arms. I wanted to bust out crying right there. It was the worst feeling in the world. They wheeled me downstairs and it was all I could do not to bawl all the way down....I was choking back tears the whole time and had my head down. My parents got me into the car....packed the stuff in the trunk, Allen got in the back with me. As we drove away I cried so hard, I didn't think I even had any tears left. I was supposed to be holding my baby, I never imagined I would leave the hospital without her in my arms. It was an awful, horrible moment in my life....the car was quiet except for my sobs. No one really knew what to say, and silence was really what I needed anyway. Allen just held me.

We got to my house, I took another shower and tried to make myself as presentable as I could. Right as I came out of my room from getting ready, my sister Deborah arrived. She looked at me and said "what happened to you?" At first I wanted to say "uh where were you last night?!" Quickly I realized she didn't mean it that way....I knew I looked like death warmed over...I had bags under my eyes and they were so swollen from crying. I am sure she was shocked to see me look so awful that she just blurted it out. We have joked about it since then.

I wanted to pump....well I didn't want to pump really...I wanted to breastfeed but I wasn't able...I knew I NEEDED to pump. I went into the nursery and sat in the rocking chair and cried. Here I was with this machine on my boob, when there should have been a baby. My sister came over and sat with me while I pumped. Allen came in too. They talked to me and it helped to distract me from what was going on. I wasn't getting really anything out but a couple of drops here and there....great I thought I can't even make milk for my sick baby. I realize now that the next morning after you have a baby your milk hasn't come in but I was already beating myself up for everything that was happening. I needed someone to blame and I was that person. I carried Makily, my body helped to form her so it was my fault. I took my meager 3 or 4 cc's of breast milk....put it in a baggy and we headed to the NICU.

I was nauseas the entire 30 minute drive there. I wanted to go and didn't want to go at the same time. I was terrified of what I may be told, what I might see....but especially how I would react to all this. I was already thinking things that I didn't understand. We got there and Allen went through the routine....Scrub your hands, put on the yellow gown. We walked to the back of the NICU and there she was. She looked as bad as she had the night before BUT this time I noticed yet another problem. Her head looked like someone had hit her with a hammer. She had a HUGE dark bruise in a circular pattern with blood caked in her hair. I was appalled and demanded to know what it was! The nurse said it was from when they used the vacuum suction at delivery. I said THEY NEVER USED THAT ON HER!!!! She then said that it was trauma from the delivery then.

"Trauma from delivery".

Another reason to blame myself.

She was on a ventilator, her nose was bloody and so was her mouth, they had a hard time intubating her. Her face was very puffy and swollen. I would touch her and her oxygen levels would plummet, her heart would start to race. The nurse told us not to touch her anymore. How can a mother look at her sick child and NOT touch her? I felt awful that my touching her would make her sicker, I kept telling myself Makily didn't like me. (I know this is extremely foolish and silly but I was nuts at the time) I was convinced she hated me for a long time.

We stayed in a hotel about two miles from the hospital the first two weeks. When Makily was about three days old, we got up that morning and Allen had a message on his voice mail that said "Mr. Caldwell, I just wanted you to know that Makily started to have a real rough time last night so we had to increase her oxygen and add another gas called Nitric Oxide." She had severe pulmonary hypertension (due to all the meconium). Her lungs did not want to stay open. I have since read that most newborns with a severe case of pulmonary hypertension such as Makily's usually die. She pulled through though.

When Makily was six days old, the geneticist came in to talk to Allen and I. I saw him walking into the NICU and thought he looked like a very important man. He approached us and introduced himself. Then he did something strange, he looked at the ventilator and asked what it was. I said "uh it's her ventilator". Strange I thought, this man is a geneticist and doesnt know what a ventilator is. He looked at Makily and then asked Allen and I a lot of questions, including if we were related. I wanted to laugh but I looked at him with a straight face and said no. (I guess some people answer yes to this!) He went to go get Makily's chart and when he walked away Allen said to me "Did he REALLY ask what her ventilator was!?" I said "yes Allen he did" We both laughed at this and Allen said "Well if he comes back and starts examining Makily's dolly saying well let's see here, her hair is rather yarn like and she has very pasty skin, we are running out of this place and quick"......we both became hysterical laughing at this, my husband amazed me that admist all we were going through he still knew how to make me laugh and smile, our sense of humor was still in tact. We quickly composed ourselves as the geneticist walked back to Makily's crib. He asked if we had any other family members that had any type of possible genetic issues. I did. My Grandmother had a little boy back in 1940 that died when he was three days or three hours old (I get different answers). He had half a kidney, cleft lip and palate, heart problems, lung problems etc. My Grandmother was told he looked so bad that she wouldn't want to see him. The geneticist said this was "noteworthy". He stated that the blood work for Makily should have been back at that point and he would check on it. He mentioned there were several different syndromes she could have and he just didn't know what it was without the blood work. I asked him the question I was dreading the answer to. "Is it possible she has no genetic problem and just has a cleft with some skin tags?" He said he doubted it, that it was unlikely. I had been holding on to the small chance that Makily would be normal until that moment. I let go of that fantasy....I felt an ache in the depths of my soul that no words can describe at that moment.

Allen and I went to eat lunch. We were talking and he told me he had no clue what the geneticist was talking about. What did all this mean? The only way I knew to explain things to him was to explain Downs Syndrome. How Makily could have something like that. I saw tears well up in his eyes and I realized then that until that moment he had thought Makily would be normal. I wanted to run screaming and crying out of there. Allen has been through so much in his life and I so wanted to give him a happy "normal" family. I had so terribly failed. Seeing the look on his face when he realized what I had already been assuming those six days was torture for me. I couldn't eat. That was a new problem I had been having. If you know me at all I love food, love to eat. That whole week I would stare and food and just become nauseated. My family forced me to eat as much as I could.

Anyway, after our awful lunch I went to go pump (this was another thing that was consuming me, I was attached to the milker all the time). I got there and someone was already in there. There was another "pumping room" on the 9th floor so I went up. I got in there, closed the door, turned off the light, got on my hands and knees in the floor and sobbed. I put a pillow over my mouth and screamed and sobbed some more. I kept saying "God please don't do this to me, please Lord I can't have a sick child....please God Help me, you know I can't do this, I don't have it in me, I am not strong enough, I didn't choose this path and I don't want to live this kind of life, please let her blood work come back okay, I am begging you God". I pulled myself together after about 10 minutes of this and I pumped again while crying. I went back downstairs and walked into the NICU. I noticed Allen was not at Makily's bed and quickly realized that it was shift change and parents weren't allowed in there for that hour. I started to rush out because I was afraid I would get in trouble for being in there. As I was walking out I saw the geneticist standing in a circle with Makily's doctor, 2 other doctors, nurses, social workers, and Makily's chart in their hand. They didn't see me, but I quickly came to the conclusion that "they knew" what "it" was. I suddenly felt like everything was going in slow motion, I could hear my heart beating...no pounding in my chest. I couldn't catch my breath. I ran down the hall looking for Allen, I was having an anxiety attack....I was shaking, my chest was heavy, I wanted to throw up. Finally Allen stepped off an elevator with the same frantic look on his face that I had. He said they had came to him and told him they had the results and were going to give them to us. My anxiety level was through the roof.....I called my mom hysterical and said you need to pray like you never have before in your life because they are about to tell us"......then I hung up.

Allen and I stood in the hall waiting for the doctors. I remember pacing and saying "please God, please God, please God" over and over....my mind was frantic. I knew the next hour of my life would change EVERYTHING forever and I was so afraid. I kept seeing people getting on and coming off the elevators, totally oblivious to the fact that my world was crumbling, they were living a normal happy life and there I stood, in hell. The world was going on with life and I felt like I had been kicked into some different reality. It was very strange. Finally the doctors came out and we sat down in this room with a long table. It was Allen and I, the geneticist, his assistant (she was an idiot), a social worker, two of Makily's nurses, Makily's doctor and some other woman. The geneticist began with these words "Makily has Trisomy 22, a 3rd copy of her 22nd chromosome." Then they handed me a "hand-out" if you will. I remember thinking "your giving me a hand-out, could you be any more lame at this moment?" I glanced at my nifty hand out and saw the words skin tag, cleft palate, heart problems, kidney problems....I had to stop reading. I asked the doctor what all this means. The next words he spoke felt like a dagger through my soul.

"Makily will be severely mentally and physically disabled."

My world stopped again, I began to cry and tell Allen I was so sorry, he was doing the same. I some how formed the words "will she walk?" he said most likely not. I then asked if she would talk and he told me "most children do not". Other than Makily dying I could not think of anything any worse he could have told me. I wanted to know how this happened. He told me that it could be just a spontaneous genetic abnormality OR one of us could be carriers and passed this to Makily. I asked if it was possible that is what took me so long to get pregnant and he said "yes usually babies with trisomy 22 are miscarried before you even know you are pregnant". I knew immediately at this point I was a carrier. The combination of the fact it took so long for me to get pregnant, my grandmother had a baby with the same problems, it was too much of a coincidence. A blood test a week later confirmed my this.

I was a carrier I had given this to Makily.

It was too much for me to handle.

I imagined Makily's life.

When he said the word SEVERE I thought what EVERYONE thinks a "severally retarded" person is like. I assumed she would be in a vegetable type state, she wouldn't know there was even a world around her. I imagined a child that just laid there and responded to nothing.

We went back into the NICU and stared at Makily. I had no feelings for her.....which made me feel incredibly guilty. I wouldn't have dared tell anyone that is what I was feeling at the time.

I was so ashamed.

What kind of mother is told she has a sick child and then emotionally shuts down and rejects her? They asked if we wanted to hold Makily.....she was still on the ventilator and had a UAC line in but I think our nurse felt sorry for us. I held her for a little bit and then Allen got to hold her for the first time. It was a very bittersweet moment.

My Mom arrived, Dad had dropped her at the front and he went to park the car. Allen went to go wait down stairs to meet my Dad and I stood with my Mom in the hall waiting for the social worker to open "the room" back up so I could tell my parents the awful news. I knew my mother was probably sitting on nails waiting to hear so I said,

"I am not going to make you wait anymore I know you are worried, Makily is retarded."

The word retarded kept echoing in my brain. I know this wording is so terribly harsh but I had no other words at that time, I was out of my mind. Just then the social worker came and let us into the room. We sat down and my mom said she didn't believe it. I was so bitter I said "well that is what they said and I believe it, I have to accept this and deal with it, I wish it wasn't true but it is and that is it". My mom insisted that Makily would walk and talk, we were both crying now. My Dad came in and I asked Allen if he had told my Dad...he hadn't. Great I get to do this again I thought. I looked at my Dad and said with tears in my eyes "she's retarded". I saw his eyes well up and he said "how bad?" I said "severe". He hugged me while I cried and kept saying "I'm so sorry, it will be okay".

This was the worst day of my life.

This is Makily the morning after she was born.Image hosted by Photobucket.com

Tuesday, November 08, 2005

I guess I'll start at the beginning...

I figure in order to start off this blog I would need to explain our story up until now. I have been wanting to do this for a while but time and emotions usually got in the way. The story really starts about 2 years before Makily was born really. I won't go into too much detail there though but I will touch on the important things. Basically my husband Allen and I started trying for a baby in May of 2002. I am one of those neurotic people...you know the kind...when they get their minds set on doing something important they are determined to succeed. Conceiving a baby took over my life. After we had tried for 6 months we had some preliminary testing to see if anything was wrong....I was told I had a hormonal issue and was put on a mild fertility drug called Clomid. This drug didnt work out for me and caused more problems than it helped. I was referred to a specialist who reviewed my labs and said that I had NO hormonal issue....keep trying, that if I wanted to do genetic testing or a few other minor tests at that point I could BUT his advice was to keep trying for another 6 months. I switched OBGYN's (since the first one had misdiagnosed me with hormonal issues that I DIDNT have) and had some x-rays that also came back fine. The end of June 2003 I had a laparoscopy that revealed I had a tiny adhesion on my left ovary, which was repaired....other than that....I was "normal"....in fact the words the doctor used was "you have pristine reproductive organs". Wow Pristine I thought...that's REALLY good! We again were urged to "keep trying". On July 25, 2003....before I had even missed my period a blood test confirmed that PRAISE THE LORD I was pregnant. I think it is important to point out the fact that this day was ALSO Allen's birthday. It was a sign from God telling me to be faithful and that his timing is always right. I had a normal pregnancy....well I did walk on eggshells...after being told I had a fertility issues, trying as long as we had, being on fertility drugs for a short time....I was paranoid I would loose this blessing baby that I was carrying. No caffiene, no excersize(that didnt bother me much ;-), took my vitamins and had been taking folic acid for 2 years at that point! I walked the line....I was determined that if anything happened I would have no reason to put the blame on myself. I remember distinctly when I went to my first OB visit. They give you a ton of paper work to fill out. When I came to the question if I wanted the triple screen (genetic testing) I couldnt answer it. I stared at it for a long time and finally when I realized I was wasting time I went to the next question. I never went back to that question. Back then I remember thinking in my naive mind that even if something was wrong with my baby I would not terminate....I still believe that but I think that knowing ahead of time is VERY important. My pregnancy was pretty good, I gained the 30 lbs, had the puffy feet, waddled and glowed. I was over the top excited....especially when my ultrasound revealed I was having a girl. I had dreamed of a little girl that looked just like me....a head full at jet black hair and big blue eyes. Everywhere I went people would stop me and say how much she looked just like her mamma and how beautiful she was. This was a dream I carried really all my life. It was finally happening. I told Allen several times during my pregnancy that things were too perfect and I was waiting for an anvil to drop on my head. My life was going just as I had planned and I couldnt have been happier. I was about 28 weeks along when I asked the midwife (I had to see her at that particular visit) when I was supposed to have my triple screen. No one had verbally asked me and remember I never checked yes or no on my paper work. She asked if my doctor had offered it and I told her no. She then said that I was too far along to have it done at that point and usually they didnt push that test much and it wasnt really usefull unless you planned on terminating according to the results. We didnt so my mind was at ease at that point. 8 weeks later I went in for my 36 week appt, I was seeing the midwife again this visit. She felt my belly to check Makily's position and noticed I had a huge lump under my right boob. I told her I was convinced that it was Makily's head and she was breech. She wasnt sure and so she sent me for an ultrasound. Before we left I asked her about the baby turning at this point in my pregnancy, I did not want a c-section. I had dreamed of my labor and delivery for a long time and I was determined I would have the dream birth I had imagined. I wanted Makily placed on my tummy right after so I could watch her breathe her first few breaths, I wanted to breastfeed right away. She said it was still possible Makily could turn and to see what the ultrasound revealed. On the way to the radiologist I remembering saying this to Allen "I am so excited we get to see her again but what if they see something wrong?" He laughed at me and said that everything was fine and to stop worrying. When they did the ultrasound they saw Makily WAS head down thank God and that the lump was her knees. She was measuring about 5 lbs then. I was concerned, I felt that she was to little, but they said the last 4 weeks she would gain a half a pound a week and not to worry. I felt a bit uneasy but tried to push it into the back of my mind. I had no idea that in just a few short weeks my "bubble" was going to be burst and I would be forced to adjust to a new life.