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Wednesday, May 30, 2007

Great developmental news and SMILES!

Today was Kaitlyn's 18 month NICU Developmental follow-up.

Actually, I've started feeling really positive in the last few weeks as to Kaitlyn's developmental progress. I feel I'm a bit afraid to jinx it or something, but Kaitlyn is actually talking! It's very faint, and most words sound fairly similar. but Kaitlyn is talking (which means communicating) and her signing has increased a lot too.

Maybe Kaitlyn knew how scared I was getting from my post a month ago and she knew she had to get "going" as mom was getting really worried.

At her NICU follow up she was only delayed in most areas by a few months. We were ecstatic. I sadly couldn't go as I've been swamped at work. I'll have to wait to read the report when we get it...but Brian was really, really happy.

I also captured a few rare smiles today. She's been smiling a lot more lately. Giving me kisses whenever I ask for them. My heart is just swelling of this webpage...can you feel it?

And, drum roll please, it's been 3 days since she's vomited! This is an all time record.....3 whole days, wow this is what it feels like to not clean up vomit all the time!

Here is Kaitlyn's signing vocabulary:
-ball,
-dog,
-hat, phone, dad (the last 3 are all the same, they aren't supposed to be the same, but K signs them the same),
-drink, eat (ha- funny that she knows these 2),
-bird, duck (she signs these 2 the same),
-bath
-more,
-all done, (but she doesn't sign when she is all done or wants more)
-she just picked up baby 2 days ago.

Here is Kaitlyn's verbal (quiet, but YES verbal) vocabulary:
The whole "talking" thing happened so nonchalantly, I didn't really realize what a huge accomplishment this is and how much she had actually started saying.
-ball,
-papa,
-mama, (she's finally calling me mama instead of papa!) Yippee
-apple (very hard to explain how she makes this word sound, she says: "app"then she breaths in to make the "uple" sound, I can't make the sound myself, I have no idea how she does it. You can hear it yourself on the video.
-baby
-diaper
-paper
She will also really try to imitate many words we say, they all sound similar when she tries, but she really is trying, this is great news.

Have to keep this one short, but wanted to share you the good news.. I"m going to post a video too, it's poorly lighted, but it's really wonderful to see (and hear!)

We've got a way to go in terms of pointing and her averting her gaze from us...but we are heading in the right direction. The NICU follow-up feels a lot of her delays may be from her vision issues, and her glasses have started helping her for 2 months now so she has a lot of "catch-up" to do from all the time she couldn't see.

Be prepared for some AMAZING smiling beautiful pictures below...really, prepare yourself..first the old standby serious girl face:
Then swimming with my dad this weekend:
Then just a few hours ago, playing with a toy that really makes her smile...get ready......

and finally........My heart is swimming as I look at this picture (I'm guessing you, my loyal readers will feel the same way):


Saturday, May 26, 2007

Mic-key party!!

100,000 page views!!
I just realized that my blog counter just hit 100,003!!

Hard to believe that so many of you check in on our story regularly. Don't forget to let us know who you are if you haven't signed our guestbook post yet.
Guest Book

on to the Mic-key party:
Well, we finally planned our first ever gathering of all our tube-fed kiddos for a play date. I belong to a tube feeding support group in San Francisco. 5 of us moms have become very close friends, leaning on each other for support, ideas and understanding.

Sadly, one of our moms, Sara, is leaving next month - Her husband has a job transfer to St. Louis (so any St. Louis readers out there, let me know!). It was hard to schedule but we finally arranged a play-date for our kiddos. We met at a park, but typical spring/summer San Francisco style, it was windy, foggy and basically freezing, so we impromptu went to one of our members house (Heidi) for the gathering.



Not an easy feat, but we captured a picture of all 5 of our kiddos: Mitch (3.5), Tyler (2), Jake 2.5), Kaitlyn (1.5) and Elizabeth (1.5):
Trying to get all 5 showing their mik-key g-tubes was even harder!
We at least got 4 on the couch at the same time, showing off their buttons. Can you just imagine the room, we were all sitting around, with syringes, food, burp cloths. What a party! :)Here we are, a group of women I admire very much. Judy (Jake's mom), me (Liz, Kaitlyn Elizabeth's mom), Elizabeth (Tyler's mom), Sarah (Elizabeth's mom) and Heidi (Mitch's mom). If you didn't catch on, Elizabeth is a common theme with our names. Thank you my good friends...you all mean the world to me..thank you for all of your support and understanding.... and we'll miss you terribly Sarah! You better keep in touch!

Kaitlyn has suddenly realized that she no longer likes her mom to leave. She's suddenly become very clingy to mom and cries when I leave her - even if I go to the other room and shut the door. Here's a few pictures to show you the tears. I have to say I'm not complaining, Kaitlyn never really has shown much bonding with me, so this brings joy to me (much to dad's disappointment). When Brian comes home from work now, Kaitlyn runs to me and begs to be picked up.
Look at the pouty face. Breaks my heart!
And of course tears (remember that the crying is quite silent with her vocal chord paralysis)
Taken on Thursday. We went out as a family to the Farmers Market which is on Thursday evenings. We stopped for a quick refreshment. Typical serious face for Kaitlyn.
Dad giving Kaitlyn some love.
Kaitlyn (looking at dad's lips not eyes which is typical) likes to imitate fish faces.
Best news of all, though, is that Kaitlyn likes to give kisses!!! When her little lips brush across mine with a kiss is the most wonderful experience I could have ever wanted in my life.

Happy Memorial day weekend. Please be sure to think of all those who have given their lives for our country, and for all the angel babies up in heaven with them.

Wednesday, May 16, 2007

Happy Mother's Day!!

My 2nd Mother’s Day:

My dear husband came home from work on Mother’s Day with beautiful tulips, a wonderfully sweet card and a picnic lunch.

Ok, maybe this is too weird or personal, but Brian’s card to me was so sweet I had to share:

“Dearest Lizard,
I cannot express enough how special you are to me. You are such an incredible giving person. Our daughter and I are sooo lucky to have you looking over us.

All of Kaityln’s progress is due to you and all your efforts – she could not have a better mother. You continually impress me with all that you do for us. On this special day, I just want you to know that I could not ask or even dream of a better mom for Kaitlyn. Oh yeah, and not too shabby a wife either! Love Your Husband.”

I had to show a house in the morning first, but then we went down to the beach to have a picnic lunch. This was Kaitlyn’s first experience at the beach.

Boy, did she HATE the sand. (once again a typical sensory issue). She didn’t’ like even walking on the beach towel, she insisted on climbing on top of me (she rarely climbs on me). Eventually I put her shoes back on and she finally (with much trepidation) ventured onto the sand. After awhile, I took her shoes off again and she felt ok this time about walking barefoot on the sand. (I spoke to Kaitlyn’s PT about this and she said it’s exactly what therapy you should do with someone with sensory aversions). But she felt positively that she did go onto the sand. As super strong SPD cases would never go onto the sand even after all the processes that I went through.

I have to say that picnicking on the beach with a toddler is NOTHING like the nice relaxing picnics Brian and I used to have. It was not the least bit relaxing actually. The beach wasn’t all that warm (typical for northern California), and with the sand and the very active toddler, and the feeding tube it was a bit crazy actually. But it was nice to be outside, not working and enjoying our daughter for Mother’s Day.

Happy Mother’s Day to all of you too!

Kaitlyn “flunked” out of feeding therapy.

Well, I guess our progress of a month ago has gone away entirely. Kaitlyn is now refusing again to eat anything. She’s at least drinking a bit of water and/or juice.
Kaitlyn’s feeding therapist suggested there really wasn’t much more she could do (I agreed) and that Kaitlyn should probably be seen by an OT who has some specialty in SPD (Sensory Processing Disorder), as her feeding therapist agrees with me that there are some sensory based issues taking place.

Just like so many of my faithful blog readers have suggested. (Thank you for all of your comments by the way, I read each and every one of them, I’m sorry I just have been too swamped with work to respond lately). I’ve gotten the 2 bible books on SPD and don’t see Kaitlyn fitting into the neat categories that describe the different types of SPD. Not sure exactly what that all means. Maybe she’s still too young to tell. Maybe her behaviors are just toddler behaviors. Maybe it’s a degree of both. Who knows.

I have been contemplating taking Kaitlyn to an inpatient feeding therapy (well at least researching them), as I feel she needs some intensive longer-term therapy to get over her oral aversions (or complete refusal to eat).

Some good news to share: I posted that Kaitlyn failed her feeding therapist onto the Micro Preemie Support group that I started. http://groups.yahoo.com/group/PreemieBlogMoms/
And Emily (one of our members) responded with a clinic program that could come to the house! I immediately went to the website: http://www.clinic4kidz.com/ and discovered that they do travel to California. I contacted the organization and the founder/Dr called me and I then discovered that not only did they travel to California, they were actually moving from Texas to California… AND…..They are moving to Marin County, which is where I leave. Their new office will literally be less than 5 miles from my house! Wow!

I already have an appointment for the first step, for the Dr to come to my house to do a long evaluation, and then follow-up with an intensive 4-5 day program. I hope and pray that I can get my insurance to cover this….I don’t have a choice, Kaitlyn HAS to take part in this program….no matter what the cost.

I am soo excited I can hardly stand it. I liked the program as they work within our environment, they look at the whole picture of the child (sensory issues, autism, medical, psychology), everything. This is EXACTLY what Kaitlyn needs! I’m thrilled.

Our evaluation is mid June. I cant’ wait!

A funny thing happened today. My nanny came home from the park and told me that she met a mom there who knew Kaitlyn because of this blog! She knew Kaitlyn had a twin sister Corinne. If my fellow park-goer is reading this, be sure to comment here on my blog!

Some Pictures to enjoy!

Brian plays hockey with the San Francisco Fire Department Team. I took Kaitlyn to watch a few weeks ago. I felt like I was in the TV show: "Rescue Me" http://www.fxnetworks.com/shows/originals/rescueme/. A firewife, watching the fire department team with other fire wives routing the team on....
A picture of the fire wife and daughter routing dad on.Well, I guess it's not ordinary fire wife stuff. See all the specks on the glass? That is Kaitlyn's food. As I was trying to push her food into her gtube, it got clogged and back-fired all over me, Kaitlyn, and the glass. If I wasn't so embarrassed (I hadn't yet met the other fire-wives), I would have laughed more. I was COVERED in food. It was all over my face, clothes, everywhere! Ugggh.. Hey, at least it wasn't vomit!!
Kaitlyn LOVES to put things on table tops. Here she is with her shelf (we had to move the phone book and other items that used to sit there). She's helping me with my real estate papers. I'm not really sure why both her tags are sticking out, her pants are rolled up as they are too long, as she' too little.
Here she is carrying around her bag of Flax Seed. (This is an ingredient to her Real Food Blenderized Diet that we feed her)
A close of up the flax seed.Kaitlyn has taken a liking also to this small pillow. She loves to rub her face and head on it any chance she gets. The bag of flax seed and the pillow are both a bit heavy and we caught her walking around carrying both - it was very funny - she's always very busy.

Mother's Day at the beach. This is typical Kaitlyn form. Not wanting to be held, squirming to get away. This was after she climbed up on me as she didn't' want anything to do with the sand.
Squirmy Kaitlyn.
Much happier cruising around
Mom and Kaitlyn on a walk with her Easter egg.

A close up of Kaitlyn and her dad.
Maybe some day Kaitlyn will become a surfer chic!
Feeding Kaitlyn on the beach. Not an easy task.
Dad is "pushing" food here just as Kaitlyn is trying to make a get-away.
Not really a fan of her hat. This was the best Mother Daughter picture we could get on Mother's Day.


Wednesday, May 02, 2007

Feeling down and depressed

Want to know why?

I'm really quite convinced that my daughter has serious developmental issues that the many therapists she sees seem to gloss over, "she's doing so much better" they say. I don't think I'm imagining this.

Here are some things I notice regularly:
Kaitlyn is almost 16 months adjusted

-She has never pointed or indicated that she wants something- ever
-she doesn't try to get me to help her - ever
-Although she will smile and walk towards me and say "papa" if I come in from outside - as soon as I pick her up she refuses to look at me and arches and wants down
-She often likes to rub or bang (not very hard) her head against things, this makes her smile sometimes
-She walks around repeating sounds, like "hmm,hmm" over and over and over, more of a whine that baby gibberish
-it is very hard to get her to look at us
-she still really doesn't like to be held- she becomes very agitated and upset
-babies /toddlers I see when held by mom hold on to mom, kaitlyn really doens't hold on to me-
-she'll usually respond to her name (a very good thing, as this is a big autistic trait) but there are times when she completely igornes you (this seems beyond just toddler tuning out to me), it's like she has no idea you are right next to her calling her name repeatedly

That's all I can think of for the moment.

In a month she has another NICU developmental follow up.

Here's a link that will show you why I feel sick to my stomach.

Enough said.

http://www.prematurity.org/research/not-catchingup2.html

Tuesday, May 01, 2007

March of Dimes Walk

This is the only picture I have right now of the March of Dimes Walk in SF. (My friend (in the background) took more, but I don't have them yet). I forgot my camera in my RUSH out the door. I left my house 30 minutes before I was supposed to be on stage and talk! I made it, but boy was I stressed. I took this picture with my camera phone of Dad and Kaitlyn on the city streets of SF on a rare sunny day.

The talk and walk were great, I teared up a number of times, how embarrassing, but everyone said it was ok, as it made the emotions and reality of having and loosing a preemie a reality.

More soon!

Liz

Saturday, April 28, 2007

What an honor!

I'm rushing around this morning getting kaitly's syringes filled with food, packing her diaper bag and stroller into the car to get ready to take her to the March of Dimes Walk America walk!

I've been asked to share my girls' story up on stage before the walk begins!

Wish me luck and if you haven't donated to this great cause, you can still do so even after the walk is over.

Here's the link again:

http://www.walkamerica.org/personal_page.asp?w=687803

Thursday, April 26, 2007

How Preemie moms are chosen

It's 11:30 pm, Kaitlyn has just turned ill, she just threw up - (normally vomiting is nothing out of the ordinary with Kaitlyn , but she hasn't at night for well over a month), her nose is stuffed up, she's crying, sneezing and inconsolable....

A fellow preemie mom (Stacy) just sent this to me - I've seen it before, but her timing couldn't have been better:

~*~How Preemie Moms Are Chosen~*~
(Erma Bombeck)

Did you ever wonder how the mothers of premature babies are chosen?
Somehow, I visualize God hovering over Earth, selecting his instruments for propagation with great care and deliberation. As he observes, he instructs his angels to take notes in a giant ledger.
"Armstrong, Beth, son. Patron Saint, Matthew.
Forrest, Marjorie, daughter. Patron Saint, Celia.
Rutledge, Carrie, twins. Patron Saint...give her Gerard. He's used to profanity."
Finally, he passes a name to an angel and smiles.
"Give her a preemie." The angel is curious. "Why this one, God?
She's so happy."
"Exactly," smiles God.
"Could I give a premature baby a mother who knows no laughter? That would be cruel."
"But does she have the patience?" asks the angel.
"I don't want her to have too much patience, or she'll drown in a sea of self-pity and despair.
Once the shock and resentment wear off, she'll handle it.
I watched her today. She has that sense of self and independence so rare and so necessary in a mother.
You see, the child I'm going to give her has a world of its own.
She has to make it live in her world, and that's not going to be easy."
"But Lord, I don't think she even believes in you."
God smiles. "No matter, I can fix that. This one is perfect She has just the right amount of selfishness."
The angel gasps, "Selfishness?! Is that a virtue?"
God nods. "If she can't separate herself from the child occasionally, she will never survive.
Yes, here is a woman whom I will bless with a child less than perfect.
She doesn't know it yet, but she is to be envied.
She will never take for granted a spoken word.
She will never consider a step ordinary.
When her child says momma for the first time,
she will be witness to a miracle and know it.
I will permit her to see clearly the things I see--
ignorance, cruelty, prejudice--
and allow her to rise above them.
She will never be alone.
I will be at her side every minute of every day of her life
because she is doing my work as surely as she is here by my side."
"And what about her Patron Saint?" asks the angel, his pen poised in the air.
God smiles. "A mirror will suffice."

Wednesday, April 25, 2007

Easter Pictures

Kaitlyn, my mom and Kaitlyn's 95 year old great step-Grandpa George.
Kaitlyn learning to "drive" a neighbors toy Barbie car. I think she's a natural!
My mom Corinne, my step-father Rich and Kaitlyn (who didn't really want to be held). Grandma Corinne didn't want to let go of Kaitlyn before our long drive home.
Kaitlyn with her "Easter spoils"
The sunshine makes Kaitlyn squint
Uncle Gary with our "Cindy Loo Who" (K's pigtails remind me of Cindy from the Grinch Who Stole Christmas)
Kaitlyn playing with her eggs.
More shots with Uncle Gary

Yes, I'm an official toddler now, running all over the place.
Kaitlyn with my good friend Diana in LA (Cute Otis in the background)
Kaitlyn's cousins Charlotte and DJ. DJ is Kaitlyn's exact adjusted age.
Dad helping Kaitlyn with the grass. K wasn't a fan of the grass at all.
Kaitlyn learning how to open up her Easter eggs.

Friday, April 20, 2007

Help prevent premature births...



Kaitlyn McCarthys' holding her angel sister Corinne's hand on the day they were born. Together for the last time.

Kaitlyn a few days after she was born, wearing dads wedding ring on her foot



Kaitlyn on Halloween, 2005

Kaitlyn Today


Can you believe that it's been a year already since Kaitlyn first came home from the hospital and we walked last year to help prevent Premature Births and birth defects? Last year I rose just over $2,000!

Before my life changed forever in 2005, I saw pictures of tiny babies born so early and said "wow, they are so tiny," and then went about my day. My life changed when I gave birth to my twin daughters 13 weeks early on 10/4/05. They each only weighed 1.5 pounds. As you know, our first born Corinne didn't have amniotic fluid for 10 long weeks and sadly her lungs didn’t develop and she died in my arms 3 hours after she was born. Kaitlyn today continues to suffer from the lasting effects of being born so early. After spending 4 months in the NICU, she had an additional 200 doctor and therapy visits for the first year of her life. She is doing extremely well now for how sick she was, but she is still fed 100% with a feeding tube, wears glasses, has a paralyzed vocal chord from a heart surgery when she was 4 days old and is socially quite delayed.

Please help us Walk to Save Babies:

Well it's that time again. I feel very strongly about the cause to help save premature births. I'm "lucky" as I know why I delivered my babies so early (my problems were caused from an amnio gone wrong); But many, many perfectly healthy women go into labor early every year and have no idea why.

The March of Dimes has made the prevention of Premature Births their largest campaign in helping prevent Birth Defects. Premature birth is the #1 cause of newborn death. It has reached epidemic proportions in the U.S., endangering the lives of more than half a million babies. And it's growing at an alarming rate. That's why we need you to participate in Walk America.

2 Ways to help:

Walk with us: We'd love to have you walk with our "Family Team" in names of both of our twin daughters, Kaitlyn and Corinne McCarthy. If you can’t walk with us, please help support our walk by making a donation in name of our daughters’.

Premature birth can happen to any pregnant woman, and no one knows why. The March of Dimes is in the midst of a multi-year, multimillion-dollar campaign to address this growing problem. With your support, the March of Dimes can continue to fund research and programs to prevent premature birth and other threats to babies' health.

Walk Details:
Saturday 4/27
9:00 at Chrissy Field in San Francisco
Meeting spot: 8:30 in front of the Sports Basement Store

email Liz if you'd like to walk with us so we can arrange to meet
To register to walk with our team, click here:
Walk with the McCarthys

Donate to March of Dimes:
If you are unable to walk with us but would like to make a donation in honor of Kaitlyn and Corinne, please click here:
Donate in name of Kaitlyn and Corinne

You can also donate by sending a check to me directly:
Make the check out to March of Dimes
and then email me for my home mailing address:
Liz@aLizard.com

Thank you in advance for your support, and remember, you can always check in on Kaitlyn’s progress here on my blog.

Wednesday, April 18, 2007

Kaitlyn eating WOW!!!!

A lot of random thoughts:

A lot of random thoughts: Honest and open thoughts

(The video above (poor quality, taken with my cell phone at feeding therapy stil brings tears to my eyes, major tears, flowing tears. more later at the end of this post -- In honor of my mother's birthday (now 2am on 4/18 When I told my mom of this feat of Kaitlyn's first "eating" today, she said it was the best birthday present ever! Happy birthday mom!!!! I love you, Grandma Corinne. I wish your name sake grand daughter could be here with us to celebrate your day. Boy am I emotional today. I"m going to bed.)

It’s 12:30 am as I start to write this post. I just finished hand washing 3 -60 cc syringes (like I do every night) after pushing 8 ounces of blenderized diet that I made for Kaitlyn this morning. I can never go to bed before midnight due to all the “night duties.” I’m in a very strange mood. A bit different than my normal posts, here are a lot of random thoughts…..

As I pushed (via syringe) Kaitlyn’s food tonight, I was over whelmed with such love and emotions for my daughter as she lay in her crib. I reached out and touched her hand as it laid spread out on her crib. I had thoughts earlier in the evening of her growing into a teenager, and loving and laughing with her and reminiscing of all that we’ve been through to see her into her teenage years.

I miss her sister Corinne more than words can say. I feel so sad when life is just “going” on and forgetting her sister. She should be here. Some times I feel that this isn’t real, that Corinne is still coming home to us. That she’ll be Kaitlyn’s sister. That Kaitlyn won’t be lonely anymore. That I never got my amnio. I saw a movie star just had twins. Where are my twins?

I’ve wanted to get pregnant since the moment I lost Corinne. I got my period again today. Again. No luck. Again. I feel I’m once again riding that infertility roller-coaster (but this time ever so silently). I’ve had to spend over $6K recently on dental work. Money that I could have spent toward IVF. Deals at work going sour. Money that could have helped us try IVF again. I’m 40 years old. I feel my clock slipping away. Will I ever have the chance to have another baby?. Will Kaitlyn have a sister that she should have?

Last night I became very depressed as I read a fellow preemie blogger talk about the horrible aspects of having a preemie that everyone likes to gloss over. The fact the being a preemie can have some horrible long lasting brain, learning, social issues. It terrifies me. What will my daughter be like? How will laying in an isolette for 4 months affect her? Being poked and prodded and filled with all kinds of drugs to keep her alive. What are the long term effects of all those drugs?

I get so tired of feeling like I have to explain that my daughter isn’t out of the woods. I want everyone to feel this cautionary feeling that she’s still not “ok” in case we have continued lasting effects of her prematurity. This other on line mom blogged that when her daughter was 2, she was released from early intervention that she was just fine, and now the girl is 7 and has major mental issues. How can this be? I watch Kaitlyn so closely , what is her future?

I hardly slept a wink last night. I tossed and turned and had night-mares wondering what the future holds for my daughter. All those doctors telling me to terminate my pregnancy, that I would never make it. I went 10 weeks, holding my daughters inside me, holding and wishing for 10 weeks lying in a bed not knowing the outcome. The other night it hit me; I spent almost 3 months lying in bed. 3 MONTHS!!!!!

I’ve had 3 random people ask me recently if Kaitlyn’s glasses are for “eye-protection” Some of my own family members didn’t even know she was wearing glasses. This really bummed me out.

Easter was hard. We were with Kaitlyn’s cousins (one is Kaitlyn’s exact adjusted age , he is so far ahead of Kaitlyn) He was actually searching for Easter eggs, while Kaitlyn was so overwhelmed by her sensitiveness of just trying to walk on the grass. It really hit home for me how delayed she is. I’m a horrible person for getting so bummed out by this stuff.

(As I said, this was going to be a post of stream of consciousness).

I have well over 200 emails that need responding to in my personal email inbox. I can’t get to them. I can never seem to get caught up. I deal with the work emails first always. The personal emails keep dropping lower and lower in my inbox. Technology has made my life easier and so much harder at the same time.

My new goal is to “publish” my story. I’ve started a support group for other micro preemie mom’s. I really believe this group has helped a lot of women. I want to see my story on Oprah. I know there are so many out there that need help, to know that it’s not all roses. To have a realty check, but to know that there is hope too.

Earlier this week one of our EI folks (early intervention) asked how we “feed” Kaitlyn standing up. As I stooped over Kaitlyn as she walked about the house, attached to her with the feeding tubing and pushed the syringe, I think she got the picture. This is SOOOO not “normal” parenthood.

Kaitlyn became sick again over Easter. The cough and mucus got into her lungs again. She had to go on oral steroids. My mom got too experienced a bit of our “life”. Breathing treatments. A lot of vomit. Constant vomit. My dad didn’t see any of this. They just said, wow she's great and normal, everything perfect. It bummed me out. They really have no idea what I go through. I’m a terrible person for writing this but it’s true. Not many really have an idea what our life as parents is really all about. I don’t comment much on it here on my blog. This is supposed to be roses and happy news. It’s not always. It’s hard. My life is hard. Our relationship as husband and wife is really suffering.

OK, on to some good stuff: Why I started my post on a bummer I don't know, but Kaitlyn has had an amazing, amazing week leaving me speechless:

She learned to do sign language, say some “words” and today ate ½ container of baby food!!!!!!

As I said, this was going to be a stream of consciousness post.

Just before we left for Easter weekend in LA at my mother’s house, Kaitlyn started saying “dada” (to both me and Brian). But we realized quickly that she was saying her first words. She absolutely breaks out into “dada” when I walk in to the room. How funny to be so ecstatic to be called “dada”! I don’t care! Kaitlyn has a paralyzed vocal chord. To hear her sweet little soft voice is absolutely heaven to my ears.

While in LA we visited my good friend Diana who has dog. Kaitlyn decided that this was the time start finally signing. The sign language for “dog” is to pat your hip, like you are calling a dog to come here. Kaitlyn pats her chest when we say doggie or when we say where’s the doggy, she looks at the doggy and pats her chest. It was so amazing.

I’ve been signing with her for 6 months now and got so frustrated at her lack of showing any interest whatsoever. Then all of a sudden, she absolutely got doggie.

Kaitlyn picked up 3 other signs in one day!
After Easter: Kaitlyn and I were playing with a funny “propeller hat” in front of a mirror and I kept signing hat. She smiled and smiled at this hat (I have it on video). Then just 2 days ago, I took Kaitlyn outside (it was very bright and sunny) so I put a hat on her, and signed hat. She immediately gave me the Hat sign. She did this a number of times. I couldn’t believe it!

I’ve been signing “more” with her forever, and now she’s starting to “clap” when I sign more with her. Not really the sign, but a clear indication that she’s “getting it”.

Later I tried the sign for “ball” Kaitlyn not only go the sign (close to it, it was more like clapping), but she actually said “ba” . I tried to sign “drink” with her and she tried all sorts of things with her hands, none of them resembling the sign for drink but she “got it.” I’m in awe! Something has finally clicked for her.

When I read her stories to her that night, there was a duck on the page and as I read quack-quack, she took her little fingers and opened and closed them. I couldn’t believe it. I don’t even remember when I last signed the duck sign (she didn’t have it super accurate but she got the concept). I singed it while reading, and she looked back up at me and my fingers and really tried to do the sign. It was amazing.!!!

So in one day, she started signing: hat, ball (and saying ball), more, duck and dog! I called Brian at work and told him. He laughed and said those were exactly the words our daughter needed to communicate with us! You know signing the word duck was really practical! 

Her “feeding” since returning home has been amazing, and I have credit most of it our new nanny. Kaitlyn is now being fed her food (via gtube) over 30 minutes. I blend up a batch of her food every morning in the blender. We give her 6 ounces over 30 minutes. For many this may not seem like much at all, but I have to tell you before I started the blenderized diet, we would spend 1 ½ hour trying to push 3 ounces and it was a night mare, vomit happened at every feed. Now, we can push double the amount in less than ½ the time and rarely get a vomit! Our nanny discovered the new secret that if Kaitlyn is walking around while feeding (not an easy feat to push the food as she’s walking around, but) she rarely vomits!!

What a miracle. After 3 days of this and only 1 vomit, I started tearing up as the nanny gave me the news at the end of the day. 1 vomit in 3 days!! It’s hard to really put into words how amazing this is.

Yesterday I received a call from a Dietician from the company that provides our Medical Equipment (syringes, formula, feeding pump, gubes, etc). I asked our doc to call in an RX for something called Duocal, ( a powder than can be added to food to increase the calories). A dietician called from the company to inquire why we didn’t want formula any more. I said I had my daughter on a Blenderized Diet.

The dietician FLEW OFF the handle, saying that you should never put “real food” down the gtube, it was so unsanitary, and the formulas were pasteurized and sterile and than what I was doing was horrible. I can’t really explain how upset I became and how I responded. I explained that my daughter couldn’t tolerate anything but breast milk for the first year of her life that she vomited up to 20 times a day. That as soon as I transitioned to this new blenderized diet it was the first time that we had any reduction in vomit. That when she was sick recently I put her back on her night time pump with formula and immediately the morning pghlemy vomits came back. That there was no way that I was going back to formulas and that she should read so many other moms’ stories about how we “saved” our children from the life of prescription formulas, prescribed form drug companies marketing to dieticians

Can I say how upsetting this was to me? Sorry for the rant. Kaitlyn’s new diet has been a life saver to us. At this moment (it’s 1 am now) I am typing and I just realized I don’t even have the baby monitor on to listen to my daughters possible vomit. We ALWAYS were on the alert 24 hours a day for vomit. Not any more. I’m getting some life back. My daughter didn’t vomit the entire day today. Can you image not vomiting?

Today an even more amazing thing happened:

At Kaitlyn’s feeding therapy Kaitlyn ate almost ½ a container of pears! This has left me speechless! Totally speechless. She opened her mouth. ………this is AMAZING and wanted food via spoon! She even came forward to the spoon! Whenever I’ve tried to feed her (even 2 days ago), swatted the spoon and shut her lips like there was no tomorrow.

I captured this on my cell phone video (not the best quality, but watching it again just now still brings tears to my eyes!)

I don’t know what will happen when I next try to feed her again. Maybe it was because we delayed the feed by 2 hours so she maybe felt “hungry” I think that’s the next thing for me to research.

Well, it’s now 1:30. I have to proof my typos. This is a huge 5 page stream of thoughts. Am I really going to post this? Who knows…..

Wednesday, March 28, 2007

Walking videos

I'd recommend viewing the following walking videos in order (scroll down and watch the ones I posted first, first). That will show has Katilyn's walking skills have increased dramatically over the last few weeks and since she's gotten her glasses.

walking with glasses