Wednesday, June 22, 2011

A special Father


Father is a special word to me. Any person can have children, a special man can be a father, but an even more special father is a Daddy.

The Dad that matters in my life is my husband. Because of my husband's love of my children, they have a chance in succeeding in life what really matters. Passing on generations of parenting. It's beautiful to know that my husband is creating a life-long legacy for our little girl, nurtured by his love for the Lord Jesus Christ.

We had two girls, but this was the best song I could find! So ignore the "Daddy's Boy" part and pretend it said Girl. :-)

Here's a video of Corey with our first baby girl, Cally Petroske, who came into this world a survivor.

Wednesday, May 25, 2011

Alexa's tummy trouble's


When you're pregnant, you dream of holding that sweet baby, and the world is a happy place. But then you're sent into shock when instead of you have a baby with colic screaming all day and all night, pooping blood, mucus and screaming with every feed, minimal weight gain, poor growth, and loss of energy. Alexa wanted to sleep all the time! We dealt with it with our first born, but Alexa seemed to be worse in a different way. Never did I think I'd be going through this again with my second child. Every feed was a battle. She would scream in pain every time we tried to feed her. It was so hard for me to see her in pain all the time.

It's so hard when you're already sleep deprived, with an active toddler, and suffering from PPD, to feel calm and tender when it's 3 a.m., you haven't slept for more than 45 minutes at a stretch for more than a month. For the first month and a half I bounced her on a yoga ball for hours. Then we were able to finally graduate to bouncing her on the ball in her car seat, because I found that as soon as she'd fall asleep she'd wake up if I put her in her bed.

I needed escape, but at the same time I felt bad to leave Alexa alone with her father, let alone a babysitter. I felt trapped, or doomed to be trapped with this child, whom I both loved and yet could not stand due to her incessant crying that sent my hormones and ears into over drive. My parents live 100 miles away, so getting any relief was not going to happen.

Everything we tried for her worked for a few days: switching bottles, switching donors, switching her formula, putting her on goats milk...etc..We tried everything we could think of medicinally: zantac, gripe water, medicines, pacifiers, keeping her propped up in her car seat as she slept. Nothing but only constant bouncing would help. everything only helped for a few days at a time then the colic monster would come back. Don't get me wrong here, I absolutely adore my precious baby girl. It was just harder to adore her with prolonged crying that did not give up. If she gave me a couple good days of low crying, I could recover and love her through it. But it just wore me out when I had no relief.

The only thing you can count on with colic is that your baby's going to cry, you're not going to sleep, and it will feel like the worst all-nighter you ever pulled, with no end in sight. Here's a short clip of what I deal with 24-7:







At the end of my rope, I made an appointment with a GI specialist about an hour and a half away from us. She told us that Alexa had cow's milk protein intolerence, and possible soy. We took her off donor milk and put her on hydrolysed formula. While this seemed to work like a charm, the colic came back about 5 days later. We were assured it takes time, but I just wasn't buying that. She was worse than ever...I don't understand why formula would have been better, being it's only partially hydrolysed to begin with. The only other option would be neocate, which is so expensive we cannot afford it. My insurence refuses to cover any formula even though it would be medical necessity for her.

After giving Alexa some dairy free donor milk, she stopped incessantly crying, she slept better at night, she started eating more ALOT more! Her skin was super soft like silk. She went from drinking 15-16oz a day and being so tired from lack of nutrition and sleeping all day, to drinking 24-32oz only after a few days being on the new milk.

It took 4months of damage to get her here and it will take her time to heal, but this drastic improvement says something. I am so grateful for donors, they have taken my child out of extreme pain and GI damage. I'm extremely grateful for all our donors who help/have helped Alexa in the past. She is not completely free of dairy because we do not have enough dairy free milk. We will reguarly test Alexa's bowel movements for blood to see when she is healed completely. We still need ongoing donors/donations for Alexa! Please help us!! Please take my baby girl out of pain. The longer it takes for her stomach to heal, the more long term damage there will be. Infant colitis is very painful situation.

Just at 24oz a day, that's nearly 700oz a month and 11 gallons month...bare minimum we would need for her to get off these offending proteins. Goats milk still contains casien, that offending protein, just less of it. We need to get it out of her diet if she's able to get better. She REALLY does need it, if she is to get better. There's milk available everywhere for babies, but very little dairy free and or soy free milk out there. I am still trying to relactate, but when she does not feel good, she will not nurse, sadly. I still try very hard. We have domperidone on order at our pharmacy (THAT my insurence surprisingly will cover!!) I assume she will consume more when she feels even better. We are delaying solids because of her immature and weak digestion, so we will need to keep her on just milk for atleast til she's 8 months old. If you are able to help us, please, please don't hesitate to contact us.

We are willing to drive 100 miles in the surrounding area for milk, and are more than willing to pay for shipping, reimburse for bags, and or shipping expenses. Also I have family in both PA and NJ that can be used for drop off areas.

This is what Alexa looks like when she feels good! Help Alexa get better! She's really been gaining weight and improving so much thanks to sacrificial mommies like you. Alexa just turned 4 months (she should be about 3 if she was not premature). So we have a long time to go!


Photobucket










Look me up on facebook: Kara Petroske
my email: pugsandchickens@aol.com


Wondering what's involved with shipping? It's VERY easy (I've done it myself) I have prepaid labels with UPS, and they can even pick up the package from your door.

shipping without dry ice (and ofcourse I would send you the cooler)
http://www.youtube.com/user/lauraMaMoore?blend=23&ob=5#p/u/11/OHeEFtlEo1A
shipping with dry ice
http://www.youtube.com/watch?v=xdFfek3HYwY

Thursday, January 27, 2011

our story




For every woman out there who was able to breastfeed successfully, or who was able to pump and bottle feed successfully, I am happy for you. You are wonderful and fortunate mothers.

A little bit about me. I'm a born again Christian, I am a content SAHM, I have two beautiful little girls. I'm married to the most amazing man in the world. He takes such good care of us all. He's so wonderfully in tune with me. If anybody knows us, they know how in love we are with each other. We live in Emmaus, PA. My world has been very blessed.

In the summer of 2004 while working on a retired race horse farm I noticed large bruises on my body. I also was very weak and near passing out a few times. I didn't have any insurence so I avoided going to the doctor for the longest time, until I couldn't wait anymore. At the age of 23 I was diagnosed with an incurable autoimmune disease called ITP. For an unknown reason, my body attacks my platelets like they are invaders, or foreign bacteria/virus, when my platelets are good. The symptoms are spontaneous bleeding and bruising. Platelets help your blood clot and heal wounds. Many of the treatments for ITP are the same treatments for cancer; although I have not had to get chemotherapy, many of the past treatments I have rec'd have damaging, intolerable side effects. I was diagnosed a year before I met my husband and I told him everything from the get-go and he said he was in it for the long run (after I explained to him it was non-communicable). He even took me to doctor's appointments on our dates!

The worst time I had was being hospitalized two weeks before our wedding day. My sweet soul mate drove 100 miles and surprised me while I lay in my hospital bed. I have not needed aggressive treatment for a long time now! I have a firm belief it is because my support, my hero and my love has been there for me like nobody else has. I have not had platelet counts in the "normal" range and this has made each pregnancy difficult, and high risk. ITP is a big part of my life - it's always going to be apart of me.




Why am I writing this blog? Because if you are considering giving us your precious hard-work, part of YOUR self, I'm sure you'd like to know why.

What's the story?

Two years ago (2/15/08) I had a placental abruption due to placenta previa. This was completely seperate from my autoimmune disorder, but things were much more complicated now. I was on four months of bed rest and had several small abruptions and sub chorionic hemmorages the whole time. It was not a fun pregnancy. My hubby rushed me to the hospital where I had my little girl, Cally Lynn at 32 weeks of pregnancy weighing only 3lbs 9oz. Becuase mommies pass their antibodies through the placenta to protect baby, my little handful was also diagnosed with my bleeding disorder a few days after birth and rec'd IVig until her platelet count was stablized.





I had massive blood loss, my placenta had a very hard time coming out, I was borderline hysterectomy and doctor "thought he was going to lose mom and baby". I had a vertical and recovery was very painful and hard. After two days in a morphine daze, I got up the second night to finally be wheeled in a wheel chair to see my precious daughter. Before then I had only been able to see her on my husband's cell phone, and I had said, "she's beautiful". I started pumping right away and it seemed to do well. Probably within a few days after coming home there was nothing left. I continued to pump for a streight month, only drops....hoping the milk would come in. I had to do it for my preemie. But we felt the stress level was too high to bare to keep pumping nothing. I wish I had known about milk sharing programs at the time. I was a very inexperienced first time mommy.

When we finally brought her home after 3.5 weeks in the NICU, this child went blue and lifeless in my arms during every feeding. It was horrifyingly scary! I took her to the doctor and I said I can't be alone with this child I think she might die on me! They hospitalized her for another week and figured it was severe GERD causing apnea which cut off her oxygen, causing her to turn blue. Oh, and I'm pretty sure a big part of that was caused from neosure (infant formula for premature babies).

I suffered alot of guilt, formula made my daughter sick, she was ill for two years every other week from lung infections - she now has asthma and even had to be hospitalized on her first birthday with pneumonia.


When you come to the realization that you can't do what should be normal and natural, your world and self-image come crashing down. You question your worth as a woman: You feel like there's something wrong with you and your body. It didn't help to have a sick baby on my hands either.

A couple of my wonderful friends helped me out so I could sometimes get one bottle of breast milk to my LO a day. I ended up making my own formula out of goat milk. This helped tremendously but it was still far in comparison to human milk. What a precious commodity... She's been doing so much better and hopefully is growing out of her preemie lungs. It was so difficult dealing with people who didn't understand and even threatened to call CPS (yes well meaning family members) because our child was sick so often, they felt we must have been hurting her :-(

Here's Cally's story on youtube:
http://www.youtube.com/watch?v=Ri8cpf2Tdc4




Cally is a very healthy girl. Her sickness has decreased, she's bright, active and very smart! Her preemie lungs are getting stronger by the years.









Alexa Renee

I gave birth via planned csection on 1/17/11 at 37 weeks gestation to my second baby girl, Alexa Renee. It was planned this time (not an emergency!) and wonderful. All prayers were answered. She wasn't born with my bleeding disorder, my husband could be there to cut the cord...tears rolled down my cheeks as I heard her first cry. The things I never got to experience when I had my first child. Alexa was as healthy as could be. I felt so blessed. I felt that if I was living a dream I did not want anybody to wake me up!



I prepared ahead of time! I read several books on breastfeeding, went to LLL meetings, did a ton of research on increasing supply. I was going to make it work!

As soon as I was wheeled back to my room they gave me Alexa to nurse. Alexa nursed like a champ and dispite being a tiny 6lbs and a tiny mouth she had a great latch and nursed every hour around the clock. I loved it! Isn't she a cutie?






I constantly paniced about her weight, thinking the same thing would happen like it did with my daughter. I learned how little I really knew about breastfeeding. She had lost 12% of her birth weight before she had left the hospital. We also noticed she was not having any wet diapers while we were there.

When we brought her home Alexa was jaundiced. She slept like a mummy! I read up on jaundice and I believe she had what's called "breastfeeding jaundice". It's an inability to get the jaundice out of her body because of lack of fluid. My milk did not come in til day 5 so this explains things. I am super sensitive to medications so I believe it was the anestesia I rec'd for my csection that delayed the process. Because she was too tired to nurse, I noticed a marked decrease in my supply. The sad part is I cannot let down to a pump, so I had no way to keep my supply up in the meantime until she was strong enough to nurse again.

The LC told me to try to nurse her on each side for 15 min, then use this contraption called a "supplemental nursing system" then pump on both sides for 20 min after that. Seems easy enough right?

Wrong. I lasted a few days. This was with my husband helping me almost every time. My daughter would fall asleep it was a struggle to keep her awake. We even tried putting an ice pack to her back. That was a struggle in itself. Then the SNS - the device I used with my first daughter that gave me nightmares! The SNS leaked like crazy - even popped off the cap and the only 2oz of milk I ever pumped altogether dumped all over me (I cried!), not only did it leak but my daughter had a terrible time latching and was working way too hard to get the milk out, and she'd be starving after that from working so hard. Then after that, the pumping was even worse. I didn't get barely any milk from the pump (hand expression included). My husband was stressed out, I wasn't enjoying my daughter, and my other daughter was being neglected. Night time was NOT fun doing this routine. I cried in my bed when feeding her. I wanted so bad for this to work I was begging God to help me!

I was beginning to get depressed, and decided to stop this crazy regimen. It was hard enough to care for two children, along with recovering from surgery, the adjustment of another person and all the demands that come with them, being sleep deprived and hormonally down. It would be one thing to see results by the pump....then I could keep a supply, which is just not there now.

Instead of feeling a sense of bonding with my baby, I felt an overwhelming sense of anxiety and failure while attempting to breastfeed. I spoke to a good friend of mine today, Laura Moore. I told her I was discouraged, and that every time I went looking for help getting milk I was put through the ringer about whether or not I exhausted all attempts already to breastfeed, which made me feel more like a failure. She told me about a similar situation about a friend she knew who was running into a similar situation. She told her friend something very wise, "it's ok to not do these things. Take that energy which did not give you results and put it into finding milk for your little baby girl".

That's wisdom! And this is a woman who successfully breast fed her kids but she is so compassionate that she opened the doors to understanding mommies who deal with supply problems. She donates herself and gives so much of herself to others. She was the one who told me about milk donating, when I myself had a desire to donate if I could...I wanted to because I knew what it was like not having the milk for my baby. I had met Laura on diaperswappers in the beginning of my pregnancy with Alexa.

When I gave my little girl her first bottle of donated milk, she was full and satisfied and my anxiety and guilt began to subside. The truth is that not all moms do make enough milk (low supply is real) and not all babies can nurse. It's hard to understand this when you have never had a problem brestfeeding. I'm glad though there are moms out there who are compassionate and want to help! She is gaining weight really fast and filling out her skin very well since we started her on donor milk. Although I wanted to nurse her very much, seeing her be nourished was far more important to me than the breastfeeding relationship itself.


I know that if breastfeeding did not work God would provide the donors we need. He says He has all these wonderful things in store for us, we just need to ask!

We are looking for ongoing donors in the lehigh valley area. We are willing to travel within reasonable distance for large quantities of milk. Also, we have family in the monmouth county, NJ area & border of PA and NJ (warren county) and would be able to arrange pickups or can be a drop off location. Shipping is always preferred! Feel free to contact me at pugsandchickens@aol.com

Wednesday, March 10, 2010

Sigh, my Cally is sick all the time

I really would love to keep family in the Loop, but the words of "I wanted to report you to CPS because your child keeps getting sick!" just won't ever leave my mind. I'm afraid to have family over when she's sick, I'm afraid to let them find out that Cally is still sick often. I'm with this little girl 24-7 and do everything in my power to keep her well, including a loop of doctors. Its really heart breaking to see her suffer so much. I've come to a point where I'm just going to stop exposing her to other kids as much.

Yes, being with other kids is good for her, as well as some germ exposure, but she's not just a regular kid. The more she gets sick, the worse off she is, because those lungs have not had time to recover. It looks as if she does have asthma. I have it, I also have sinus disease, allergies and all of the above. I have general immune system weakness with autoimmune disease, but I try to keep healthy as much as possible (a healthy sick person). She improves drastically in the summer so it can't come soon enough. I think at the most I will be putting her in 2s & 3s once a week instead of three times a week. I feel bad because she has so much fun in there. At the end of this month we go to the asthma doctor for allergy testing. I am really looking for a glimmer of hope here.

Tuesday, February 23, 2010

My Review of Easy-On Leather Sandal

Originally submitted at One Step Ahead

Just like children, all shoes are different. Please be sure to find the perfect size with our printable .
Our kids' leather sandals go on and off so easily, chubby little hands can do it without help! The secret? A child-friendly, hook 'n loop flap. Super comfy and lightweight....


Good quality, sizable

By Kara from Lehigh Valley, PA on 2/23/2010

 

5out of 5

Sizing: Feels true to size

Width: Feels true to width

Pros: Durable, Leather, Cute, Arch Support, Comfortable, Stylish

Best Uses: Casual Wear

Describe Yourself: Casual, Conservative, Stylish

I bought these shoes in 1/2 a size bigger for this summer. They're still half price (from last summer). Cally got a pink pair and they're sooo cute. They are leather, have good traction on the bottom, and the insides are padded and have an arch even, and very adjustable. They have the same pair but slightly different style in the new catalog for $25.

(legalese)

My Review of Cozy Crib Tent(TM) II

Originally submitted at One Step Ahead

Our deluxe Cozy Crib Tent not only prevents climbing and falling...it keeps little limbs from getting stuck between crib rails! The safest crib tent ever! Ours not only encloses the top of the crib, it surrounds the entire interior with soft, safe netting. Arms and legs can't get wedged betwee...


Peace of mind but be gentle w/assembling

By Kara from Lehigh Valley, PA on 2/23/2010

 

4out of 5

Gift: No

Pros: Roomy, Easy to Assemble

Cons: Stitching needs improveme

Best Uses: Toddlers

Describe Yourself: First Time Parent

I was concerned about my 2yr old daughter crawling out of her crib, and didn't want to wait for her to do so. She could already climb out of her play pen so I didn't want to risk it, and she is too mischievous to be ready for a toddler bed (also didn't want her to get out of her room and fall down the stairs). Although a little pricey, you have to imagine the liability this company has, so it's understandable. It was easy to put together, but a few of the stitches in where you insert the pole came loose, but we were just careful after that. It hasn't come apart any more since we put together and is quite sturdy. My daughter doesn't seem to think anything of it, and it gives me peace and ease of mind that she is safe. The dual benefit is it keeps the bugs out of her crib while sleeping (here in PA we have stink bug issues!). I don't see her in any way being able to unzip it and it is high enough over the crib where she can stand without touching the top. Another benefit is the fact that you don't need a bumper and it keeps her legs and feet from getting caught in the slots of the crib like they always did before! Definitely a worthy investment. Let's see how it holds up for the next kids. We intend to keep using it!

(legalese)

Tuesday, January 26, 2010

Allergen-Free Animal Crackers




Wow, it's been awhile since I posted on this blog. I had actually forgotten that I had a blog. I think it's a good idea, especially for all of Cally's followers to delve into her interesting little life.

I really wanted to make a blog about Cally's new animal crackers. Cally has food sensitives, dairy and wheat products to name the two major ones. I really wanted to make her an animal cracker she could enjoy. The hard part is working a recipe that is both gluten & dairy free - very difficult. I was able to find a recipe on Recipezaar, and I tweaked it. Mainly, instead of using shortening, I used coconut milk with the water removed. I think they turned out pretty good. Here's some pictures of all of it in the making. My back hurts from hunching over but it was sooo worth it!

I originally obtained the cookie cutters (a set of 9 miniature animals) from ebay (actually overseas). I didn't want them to be too detailed because it may have added extra hassle in pressing the cookie out of the cutter onto the baking sheet.

All of the ingredients were incorporated then then the dough was separated into four balls. Each ball was rolled out and I cut them out and re-rolled the ball to make more out of the trimmings.








I poked eye holes for most of the cookies to add a little more fun. The cookies were initially baked at 375 degrees for 8 minutes but I found it to work better for us to cook them for 9 minutes at 400 degrees. They still were soft after that. I figure, hey, less of a choking hazard.


I probably ended up cutting 150 or so of those little buggers.


Starting from the top left to right is a horse, a fish, then a lion, rabbit, cat, bird, mouse, pig and last but not least, a bat. Now the hard part, would she like them?? I tried them myself, they were plain and a little doughy. But what I thought didn't matter. They had to be tried & tested.


She LOVED her animal crackers. We also were able to fit some home schooling in this project. I gave her one of each shape, and with each one I gave her - I told her the name of it and also the sign language sign for the animal. It meant alot to me too that she didn't just cram them down her throat, but that she'd say the name of each one before she bit off an appendage or head, or play with them as if they were moving (ie: the bunny hopping). Not sure if it was the fact that she was late being fed lunch but she asked for more and more! I think the only thing different I'd do is next time add some orange extract or make them thinner for a crunchier version :-) Here's the original recipe, but like I did you can also tweak it to your liking. I did not buy a gluten free bake mix but I had bought all the ingredients seperately and made my own. I'll post that recipe as well.

I love the piggie the best!



Allergen-Free Animal Crackers

Ingredients

OPTIONAL

  • icing, and decorations (optional)

Directions

  1. Mix the arrowroot, flour and baking powder in a bowl and set aside.
  2. Cream the margarine, sugar and vanilla together in another bowl.
  3. Beat the baking powder, oil and water mixture into the margarine and gradually blend in the flour mixture.
  4. Bring the dough together into a ball with your hands, flatten and divide into quarters. Roll out one piece thickly on a clean and floured board with a floured rolling pin.
  5. Cut our your favourite animal shapes (or any cookie cutters you like) and carefully transfer them onto ungreased non-stick baking trays.
  6. Bake them in the centre of the oven for about 8 mins at 190C or 375°F.
  7. Remove the trays from the oven and leave the cookies to cool on the trays for a few minutes before transferring to wire racks.
  8. Decorate with icing as desired or eat plain.
  9. Makes about 30 (depending on size).


I Can't Believe It's Not Gluten! Gluten-Free Cake Flour Mix

Ingredients

Directions

  1. Sift ingredients together, combining thoroughly. Use in place of flour in cakes and other baked goods.
  2. Store in airtight container or ziploc bag in refrigerator.