Tuesday, December 3, 2013

National PKU Awareness Day

There are many reasons why I have abandoned my blog efforts for the past few months.  I cannot get into those in this post, but just know that I am trying to jump back on this wagon now!  Today is too important not to post.  Today is National PKU Awareness Day.  Ever since Carson was diagnosed it has been my mission in life to raise awareness and help people in our lives understand what it is all about.  If you love my child, you need to understand his challenges, and of course how special he is.

Carson is still doing great with his diet.  He is finally showing more interest in other foods (SALAD!!!), but he also is becoming curious about foods he cannot eat, thanks to his grabby little sister!  lol  He sees her eating what I eat and he wonders what we are eating and why he is not getting that.  I am trying my best to explain it to him and use each opportunity as a teachable moment.  He gets a kick out of saying "PKU" for some reason, I guess because he loves letters so much.  I am so proud of how far he has come, and it is so nice to be able to start to tell him and help him understand what he eats and does not eat.  This is quite an adventure!

For more information, please visit older posts on my blog by clicking on any of the PKU related topics in the list on the right-hand side of this blog and read about our experiences with PKU.  I will try my best to get back here and post some more updates and share what has been going on in our crazy, busy lives.  Happy PKU Awareness Day, friends!

Monday, July 29, 2013

My Son Has Autism

Note:  I want to apologize for being such a blog slacker.  The main issue has been that Carson damaged my laptop charger, and since it is the only computer I currently have access to, it is a very daunting task to get it charged up enough to write.  I soon hope to have a new charger and get back to more frequent posting.  Thank you for your patience!

Yes, my son Carson has autism.  You already know that?  Of course you do!  I have already written about it many times!  Why, then, you ask, did I write a blog post with this title?  As time marches on, I delve deeper and deeper into the experience of raising a child with autism.  It has almost been 4 months since diagnosis, so I am still fairly new to all the therapies and information out there.  Forgive me for sounding like such a newbie, but it is a perspective I feel should be shared with others who may be going through the same.  Some realities are only now beginning to hit me.  One of those real moments happened a week or two ago, and it slapped me in the face.  Hard.

I don't like excuses.  Everyone uses them, myself included, but I don't like to, and I don't like when other people do.  I don't like feeling like we need special treatment, but the reality is, sometimes it is needed.  I rarely have issues with Carson when we are out in public.  Usually any tantrums or defiant acts appear to the bystander, upon brief encounter, as typical for a boy his age.  However, Carson is getting bigger.  With his aging appearance comes the expectation of more mature behavior, but because of his difficulties the gap is only widening.  It is becoming more apparent that there is something different about Carson.  I have dreaded this day.

I have read about and been told by some other moms that they keep cards to hand out in public in case they have any problems.  These cards explain a bit about autism and are intended to inform the "well-meaning" strangers who may decide one day to comment about a behavior.  I have read it so many times and wondered if it would ever happen to me.  I never dreamed that I would be one of those people to carry the cards.  I'd never seen one or been given one (except for a fellow mom who showed me hers), but I also don't go up to people I don't know and comment on their parenting skills.  Now I am actually wondering if I should be a card-carrier.  I am beginning to learn that saying "My son has autism" too many times can get pretty old.

I know I said it a few times this particular day, and usually it is only if we run into someone I know as maybe a casual acquaintance, say, through work, or someone I may have gone to school with and haven't seen in a while.  Sometimes I say it when someone asks Carson a question, or if he happens to scream (which fortunately is rare) when someone approaches us and tries to talk.  But on this horrible day of days, it wasn't one of those instances that got to me.  It was something a little simpler.

Carson has a love for opening and closing doors.  If you have ever seen us at Walmart, you probably know this already.  He loves to open and close the freezer or cooler doors.  When he sits in the buggy, it is easy to limit how many times he does this.  Now that he is getting bigger and wants to walk or push the buggy, I am having to learn other ways to limit this behavior without causing a big scene.  Most of the time, so far, I feel like a failure.  Many times my attempts to stop him have ended with a mild screaming fit and Carson falling to his knees on the floor, staying there and refusing to move on with me.  I tried to drag him once, but figured that was a worse idea, so I just wait for him to get over it.  He just sits there and looks at me, which is better than screaming, but still draws a few stares.  But the incident didn't happen at Walmart.  I never have a problem there, so far, with anyone saying something to my face or to Carson.  No, this day we had gone to a small-town store to look for something a little out of the ordinary for Carson's diet.  Unfortunately, this small store had lots of coolers, and only small buggies, too small to restrain Carson.  I let him wander while I shopped, since the store was small enough I could keep my eye on him.  I tried several times to stop him from opening and closing the cooler doors, but to no avail.  And then it happened.  The man working in the store, no doubt probably the manager, walked up to Carson and told him (in a nice tone) "These aren't for playing with."  Ok, I know it doesn't sound like a big deal...but my blood BOILED.  SO many thoughts have gone through my head since that moment.  I wanted to lose my mind!

First of all, I understand that Carson should not open and close the doors so much.  It does cause the compressors to run more, which costs money in electricity.  He was not being rough, so no worries about breaking anything.  And this man has every right to take care of his store, his property.  But first I worried that he must think I'm not watching my child, which equals bad parenting.  I was watching him, and I would much rather him be doing that than getting into things, breaking things, or trying to run out the door.  He was contained, he was safe, and he was occupied.  There is no way this man understood that.  Secondly, I don't get onto other people's children, ever, unless I know them very well and they are doing something that could be harmful or that I know they are not allowed to do.  It was the first time I ever experienced a complete stranger correcting my child without my permission, and I didn't like it.  And I know it won't be the last time.  Lastly, I didn't know how to respond.  I didn't know what to do after that.  I was so angry and I didn't want to take my anger out on anyone, and I was very embarrassed at the same time.  How was I supposed to handle this situation?  I wasn't finished looking for what I needed, and I was fighting the urge to put my stuff down and leave right then out of anger, but I was also trying not to blame this man because he didn't know.  And I honestly don't know if what he did was right or wrong.  I can see it both ways now.  So I did the only thing I knew to do.  I got Carson and tried to keep him with me, which was a huge power struggle.  I ended up having to carry him myself, and since he weighs over 40 pounds, there was no way I could do that for long.  So I gave up and went to check out with what I had already.  But the man was busy helping someone else, so the girl checked me out.  Lucky for him (and me!).  I thought about it, because I didn't want to sound like I was making excuses, but right before I walked out I finally decided to tell the girl (with the man standing right behind her with a customer) to tell the man that I was sorry if that bothered him, but my son has autism and I don't know how to stop him from doing that yet.  And I walked out.  She was really nice and smiled and said something nice I don't remember, but I was red as a beet.  I was so glad to get out of there, and thought, I may never go in that place again.  We will see.

I know to some of you it sounds really simple and maybe a little silly to be so upset about it, but I was.  It still bothers me a little now.  It was a wake-up call to let me know I need to work harder to learn what I am doing with Carson.  It was motivation.  I talked to one of the therapists about it this week, and she gave me a few ideas, most I've already tried.  But a good limitation, like telling him he can only do this so many times and then move on, might work.  I did try that already, but I think I have a better strategy now.  The point is, I need to step it up a notch and start practicing all that I am learning.

The reason I shared this story was because I know there are other people out there who can relate, and there are people out there who need to see things from my perspective.  This man didn't know
Carson has autism, or that this is one of his challenges, or that I have been trying to work on this behavior.  How many times do we wish that other people only knew what was going on?  We only see a snapshot of people we meet in stores or restaurants, we can't know their whole life story or understand what is going on within them at that given moment.  The lady in her pajamas with rollers in her hair may have been just getting ready for bed and had to make an emergency run for baby diapers or something.  The baby that won't stop screaming may have just not had a nap, but it was the only time they could go grocery shopping and there was no one available to watch the baby.  Or the little boy running around that won't listen to his mommy, may just have autism and doesn't know what she is saying, but she has to take him anyway because he needs to learn how to handle it.

I don't want special treatment, I don't want to make excuses, I just want everyone in the world to take a moment and put themselves in other people's shoes before they make judgments.  That's the Jesus in me.  Now I'm thinking about being a card-carrier.  What do you think?

Tuesday, July 9, 2013

Breakfast...It's What's For Dinner

Carson has recently developed a love for breakfast foods.  After eating mostly Chocolate Cheerios, bananas, and the occasional lopro pancakes, we finally have a few more things he will eat.  I am seeing some growth here!  I love it when we can break the monotony and expand our horizons a bit.  What a breakthrough! 

Several months ago, or more, I ordered 2 sample kits from Country Sunrise.  I highly recommend anyone out there with a PKU'er to try these products!  They are the neatest thing I have ever seen!  Carson fell in love with the Universal Egg Mix.  It is just a white powder until you add oil, then water, and voila!  It turns yellow!  You mix it up and pour it in a skillet and scramble it, and it looks just like scrambled eggs.  It also has a great flavor.  The most important thing here...Carson loves it!  I admit I am as in love with making it for him.  I also tried the Hot Dog Mix, which is equally neat and pretty yummy, but sadly, he wouldn't eat it this time.  At first he did eat one I made.  I will have to keep trying.  I can't wait to try more of the samples!

With Carson's tendency to be extremely habitual and picky, I was having a hard time filling up his tummy and meeting his phe requirements.  He was hitting a growth spurt and eating everything he could and asking for more.  Because he limited his wants to only a few certain foods, I knew I had to do something and fast.  He needed to eat more lopro foods.  His current menu includes several, but he needs more variety to fill him up.  He would eat Cambrooke's Mini Pizza Pockets, lopro bread and cheese or Biscoff spread, and lopro rolls, pasta, and rice.  I also use Cambrooke's MixQuick to make pancakes and chocolate chip cookies.

The addition of the egg mix has been a lifesaver for us.  For example, today Carson needs to do a washout because his level got a tiny bit high (I assume because of that day we ate Mexican food and tater tots in the same day!  lol).  His menu is much easier to plan today for this, because I don't feel so bad about not giving him his Cheerios.  He doesn't eat them as much now anyway!  Today he will have pancakes, eggs, toast, a sandwich or pizza pockets, applesauce, cookies, pasta, and rolls.  That's a much better variety, don't you think?  I am so excited!  Now, if we could just work some more vegetables into that diet...

To order Country Sunrise samples, visit www.pkuperspectives.com.  Look for the Country Sunrise logo and find Samplers.  They have a couple of different ones; I would suggest getting both the meat alternatives and the one that includes the eggs mix.  They are very affordable and it gives you a chance to try them before you spend a lot of money.  Good luck and happy cooking!

Friday, June 21, 2013

Friday Fun: Lazy Summer Days

Cats:  The epitome of laziness!
Today is the first official day of summer, the longest day of the year.  However, most people celebrate the beginning of summer as the end of school, which happened a few short weeks ago.  And here in the Deep South, it almost always feels like summer already anyway!

So far this month, we have had lots of outdoor playtime, celebrated Father's Day, and had our first swim of the summer (pictures I don't have yet).  All this boils down to is some hot sunshine, tired kids (and tired mommies and daddies and grandparents!), some yummy summer refreshments, and a lot of fun, with more to come!

Carson being lazy...poor Maggie, he is twice her size!  My hard-working little girl!
 

Then Carson returns the favor by giving Maggie a ride in the covered wagon.
My sweet sunshine!

After a long, hot day in the sun, I tried a new recipe for a refreshing low protein (for Carson's sake) treat:  Strawberry Banana Smoothie!

Of course, Carson wouldn't even try it, but Maggie and I thought it was good!

Don't forget your shades!


It's hard to see what is going on here, but Carson and his Dada are enjoying time climbing on the hay bales!

A friendly Father's Day race between Carson and Papa Steve after feeding the horses.



Peaceful sleeping angel...summertime play is hard work!  lol

Friday, June 14, 2013

Embarking on a New Journey

I first want to apologize for not having my Friday Fun post up last week.  As you will read, I have had other things on my mind.

I love the word "embarking" because it makes me think of cruises, which is where I wish I was right now!  Somewhere south of here, on a tropical island, soaking up the sun, listening to the waves...ahh.  But...I'm not.  Oh well.

Actually, my new journey is taking me somewhere I have longed to be...HOME.  I have officially made the decision to leave my full-time working status so I can spend more time taking care of my family.  Not just Carson; my whole family, including myself.  I know there are lots of women out there who work with full-time careers, have a marriage, have a nice home, have children, and do it all.  I have always been one of those women, one who thought she could have it all.  Only I realized recently, all wasn't all it was cracked up to be.  There are parts of that all that I have finally learned I can live without, or at least want to try to live without. 

When Carson was diagnosed with autism in April, I was already feeling run down.  Maybe even since I went back to work after Maggie was born last year.  By the time I get off work, go pick up the children, get home, unload all the junk, get everyone settled in, cook supper, eat, give baths, fix milks, it's time for bed already.  I have no time for cleaning up, doing laundry, or relaxing myself.  On the weekends, I am so stressed out having both children by myself while Marty is out farming, while trying to clean up a week's worth of mess in the house, and it just started going downhill from there.  I got so exhausted.  Mommy needs a break.  I don't see how these women do it.  I have done it for a while, and it is not good for any of us anymore.  We need a break, the kids need a break, the grandparents need a break.  This life has become too exhausting.  I had to do something.

Carson's diagnosis was not the reason I made the decision, it just made the decision a little more obvious.  Knowing that he was going to need therapy gave me the motivation to give up my work life so that I could be with him at therapy.  So I could be with him and with Maggie at home.  So I could at least stay somewhat caught up on housework, and have more time to devote to cooking special foods for Carson to try, and new foods for us and Maggie to try as well, to try and live a healthier lifestyle.

This is such an opportunity for me.  I am still very sad inside about leaving my status here.  I have worked at this same job for over 12 years, and I LOVE it.  That is rare, I know.  My job has been my mission for most of my adult life.  I love caring for the needs of senior citizens, finding available help for them, providing activities for them, counseling them about insurance, delivering meals...all of that work has been a dream.  I have loved every minute of it.  I have learned so much over the years from all the people I have met, from all walks of life.  I grew up at this place, with these people.  I have been here since I was still living at home with my parents, before I got married!  This is like my second family.  It is very hard to think about not seeing them 8 hours a day.  Sometimes, coming to work can feel like my "break", but then when I have to get busy reality hits! lol 

But God told me one day a few months ago that I needed to let go of this place as part of my past.  I finally felt that I have a new mission in life:  raising my family, advocating for them, and helping others with similar situations.  I have spent so many years helping senior citizens, but my own family needs me more!  I can apply all these things I have learned about advocating to working for the best life for my children.  The second revelation was that God also reminded me of the old cliché:  "When one door closes, another one opens".  The catalyst is, the door has to close first, then the other one opens.  With my elementary teaching degree, if I ever want to apply for a job, I need to be able to get out there and work for it.  That would never be able to happen as long as I'm working full-time elsewhere.  I need time to get out and volunteer, substitute, do things in the community, get involved.  So my decision has many layers to it.

For now I have decided I will take the rest of summer off.  I will take Carson to speech and occupational therapies two days a week.  When school starts, if I get Carson into preschool as planned, I will work at my job part-time, indefinitely, while Carson is at school.  Fall is open enrollment, which is our busy season at work.  I really want to be able to help out, because I know they are going to need the help.  And it will help me too, transitioning.  But one day in the future, I know I will have to "cut the cord" completely.  I have to make peace with that.

This transition is frightening for me, but I am excited at the same time.  I look forward to focusing my attention on my family.  I think we will all be better for it.  It's the right thing for me to do at this moment in time.  I thank God for giving me the guidance and the strength and having patience with my doubts.  I also know that He will provide for all our needs, because my faith is in Him.  I am following His plan as revealed to me so far, and His path will lead me to the right places.  I am SO blessed and thankful for it!

Friends and family, I ask for your prayers, support, and advice as we make this transition to me being a new, sort-of-stay-at-home mom.  :)

Friday, May 31, 2013

Friday Fun: Random Silliness!

At the end of a very stressful week, it sure is nice to look back at all the pictures and at least remember the silly times that made me laugh!

Hello? 

The Cow and the Chicken are Maggie's favorite buddies.  She frequently gives us collections of things to hold, so this is Daddy's animal collection.

Wearing Nanny's glasses


Photography by Carson...at Walmart (Papa Steve, you made the blog!  or at least, part of you did!  lol)

Inspecting a lady bug...and talking to it

Why do boys always have to spit?

Bouncy castle fun at the autism support group picnic

Socks are my least favorite part of laundry

Icing fight with my brother on my birthday

Happy Birthday Mommy!!!

Here, put these on

Another Carson masterpiece.  Apparently, bugs can smile and say "Cheese!", because that's what Carson said when he took this picture.
TGIF!!!  Everyone have a great weekend! 

Friday, May 24, 2013

Friday Fun: Brotherly/Sisterly Love

 
As I was scanning over all the pictures from this past month, I thought about a theme that was relevant for this moment in time.  As Maggie is growing up and Carson is becoming more communicative, I love watching their relationship with each other evolve.  And then it started to remind me of growing up with my little brother.  You can see our picture on top of Nanny's piano on the far right...lol!
This month has been a really fun time for all of us.  Carson and Maggie have had many opportunities to play outside together.  Just look how much fun they have together, and the love and the sibling aggravation!
Sweet brother pushing her in the swing at the park.  Look at the happy face!

Grabbing...affection to him, aggravation to her!


What do you think is going to happen here?  Is Carson trying to run her down with his tricycle?

Taking a break (which lasted about 3 seconds!)

Every practicing gymnast needs a good spotter
Anything you can do, I can do...

My favorite...the love of a sister..."Car-Car!!!"  Wait for me!

I am happy that Carson and Maggie have each other, and I can't wait to see all the memories they will make.  I love having a brother, and I'm so thankful for all the memories we have growing up together.  It's nearer to my heart now because my brother (who is in the military) is home for a visit, and in a few days he will be leaving to go to Japan for a while.  I already miss him, but I am going to miss him so much more knowing he is so far away!  Thank God for all the great technology we have now to keep in touch!  Just having him here makes me think of all the (fun) times we have had, and making new memories with his niece and nephew.  Even making new memories for me and him.  I certainly will never forget this hand sanitizer he sprayed all over me and my desk and everything at work when he came to see me the other day!  Thanks for that!  Love you!

Ahh...the love between a brother and sister...never ends...:)  

Yes, I know, Eric, this is a terrible picture, but it is a smiley one!
(Going away party, Feb. 2010)

Wednesday, May 22, 2013

The Cost of PKU

I would like to share a little more information in honor of PKU Awareness Month.  I sometimes discuss other costs of PKU, but just realized I have not really explained the financial cost in detail.  I got my inspiration from recent posts by Kelly over at Littlest Sweet Pea .

If I had to insert a disclaimer here, it would be that all PKU families are not created equal.  Everyone has different needs, different insurances, and lives in different states where coverage and programs are not all the same.  And although most children Carson's age are picky eaters, not all of them are, and not all are as picky as Carson!  Also, there are thankfully several options available for formula and low protein foods.

Currently, Carson is covered under my insurance plan at work, which is pretty fabulous.  However, it is far from perfect for the coverage he needs. It does not cover his nutritionist visits (and they are the most important people in our lives!), which so far have been $46 per visit (we go twice a year).  And because Alabama does not have a policy to provide medical foods, unless you qualify for Medicaid or WIC (which we don't right now), we have to pay for Carson's formula.  The most important part of Carson's diet is his formula.  The formula gives him all the protein he needs minus the part his body can't process, therefore it is specially made.  He drinks the brand Phenex-2.  Presently we get one case a month of 6- 400g cans, which is about the size of a small can of powdered baby formula, in comparison.  My insurance pays 70% after a $50 deductible, leaving 30% for us to pay, which amounts to just over $130 per month!  This is our biggest expense.
   

I make him a loaf of bread about every 2 weeks, and it has several ingredients:

1 cup Wel-plan Baking Mix (made of cornstarch and wheat starch):  400g box for $9

1 3/4 cup wheat starch: CamBrooke Foods Wheat Starch is a 6lb box for $17.99 (I think one of these lasts me about 3 months)

3 tbsp Metamucil (I buy the largest container I can find, Original flavor and always brand name): 29oz container at CVS (which is where I had to buy it last) was $16.29

2 tbsp Coffeemate powder:  22oz for $4 at Walmart

2 tbsp sugar

1 1/2 tsp yeast:  Fleischmann's Active Dry Yeast 4oz jar for about $4.50

3/4 tsp salt

1/2 tsp molasses

Most of these ingredients last 3 months, 6 months, some maybe a little longer, so it's hard to calculate a total cost.  That comes to about $50 for everything, so if I bought everything 4 times a year, that's $200 (but it's likely closer to $100).  That's probably only a little more than most people who buy a loaf of bread at the store every week.  If I wanted to buy a low protein loaf already made it would cost $11.99 for ONE loaf from CamBrooke, plus since it is a cold ship item you are required to spend at least $50 minimum, then pay over $20 shipping on top of that.  See why I make the bread myself?  Plus it tastes a whole lot better!

The most used items in my house are CamBrooke's MixQuick, which I use to make Carson's chocolate chip cookies each week, and sometimes for pancakes.  A 6lb box is $34.49!  That is by far the most expensive food item I buy.  I use Chocolate Dream Dairy-Free Chocolate Chips, which I buy at Whole Foods in Birmingham, and they are about $5 for a 12oz bag (maybe twice as much as regular Nestle chips).  The other big food item I buy is low protein pasta.  He eats it almost every day.  I buy the Loprofin Fusilli from Nutricia North America, which is $11 for a 500g box.  A box of Great Value at Walmart, about the same size, might be less than $2, I don't remember exactly.  Carson eats a whole cup of pasta each time now, so one box does not last very long anymore.  These are his main staples.


Another comparison item, one I can buy at Walmart, is Biscoff spread.  This is his peanut butter alternative (which is much tastier than peanut butter!) and he uses it most days on bread to make a sandwich.  A 14oz jar is almost $4; in comparison, a bigger 18oz jar of Jif is less than $3.

Carson's only other sandwich of choice is a grilled cheese.  CamBrooke's American Cheese Slices are about $11.99 for a bag of 32 slices, versus the brand I buy for the rest of us, Velveeta, which would cost maybe $6 for the same number of slices.

The only precooked food I buy Carson is CamBrooke's Mini Pizza Pockets.  That should have been listed under his main staples as well!  The best comparison I could find is Totino's Pizza Rolls.  A bag of them, twice the size of one box of Carson's pizza pockets, was $3.29 at Target.  That contains 40 rolls.  A box from CamBrooke contains only 6 (obviously larger) rolls, for $9.99 per box.  One box lasts Carson 3 days (meals).  He eats them twice a week, so that amounts to $29.97 a month (3 boxes).

Most everything else he eats is typical stuff like we eat that we can buy anywhere, like cereal and fruit and vegetables.  But make no mistake...this is an expensive diet!

As I mentioned before, there is no assistance from the Alabama government on medical foods (which are provided to everyone, regardless of income, in many other states), nor is there any help for the special low protein foods he has to eat to fill his tummy without getting too much protein.  Insurance does not pay for those, much like a diabetic having to buy special foods (except much more expensive and much more volume!).

There is a bill that has been through Congress a few times but has yet to be passed or approved.  Every year since its inception the bill has been lobbied by various organizations supporting PKU and other inborn errors of metabolism who require such diets.  I believe the opportunity for the current session has already ended, but please click here to learn about the Medical Foods Equity Act .  Contact your local members of Congress and help support this cause in the future!



Friday, May 17, 2013

Friday Fun: Oh, BOY! What will he get into next?

Today I am starting a posting series I will call "Friday Fun".  Every Friday I will try to post some recent pictures/stories of something light and entertaining, just for fun.  Welcome to my first episode!

I have been saving up these pictures for a while just for the purpose of making this post.  I couldn't help but share all the wild and funny places we have found Carson lately! 

First of all, we are witnessing the classic older sibling regression:

Baby Walker
Baby Stroller
Baby Swing
Baby Riding Toy (bonus: teddy bear with pink tutu! lol)
Then we have the "typical" little boy stuff:
 
Not as typical as it appears:  He is not "hiding" in the hamper.  He was actually going in his room to turn on the lamp, which is beside the hamper.  How he ended up in the hamper I don't know! lol
Climbing one of the dead trees left by the tornado, at Nanny's house


Climbing onto the gooseneck trailer and then onto the pile of wood for the shed, all by himself

More climbing...up and down ladders by himself!

Pushing Grandmother's walker around...and around...and around...
 And last, this one is just for me:
I used to play this game with my cat.

 Happy Friday!  :)

Tuesday, May 14, 2013

PKU Awareness Month


Educate.  Advocate.  Inspire.

May is PKU Awareness Month!  I want to take a few minutes to shine some light on this subject that
most people know nothing about.  I have found some great bloggers recently who have really given me some great inspiration, about both PKU and life in general.  Check out my Favorite Blogs list and pay some of these folks a visit!

Feel free to check out my PKU tab at the top of the page to read some detailed info about PKU and our personal experience with it (I have updated it just a bit today).  We have such a whirlwind of things going on in our life right now, just finishing up our first Autism Awareness Month, and then running right into the same for PKU!  I hope everyone will take a little time to read about this rare disorder and tell other people about it.  Education is the first step!

I hope to devote more time to working on this blog in the near future, to make it more helpful, supportive, and useful.  I plan to add more info about traveling with PKU, which seems to be a highly searched topic, as well as eating out.  I don't have much of a need for recipes right now, so I probably won't be very helpful on that subject, though I love to read them anyway!  I also have a dream to start some kind of local PKU group.  Alabama has only a small number of people who have PKU, so I know it has not been easily done.  I mainly just want to create a place where everyone in Alabama can go to find resources, information, and support.  Any advice or wisdom would be appreciated, if you would like to chime in.

Carson and his PKU Diet


I like to give an update from time to time about Carson and his diet.  (note:  Some of this info is also included on the PKU tabbed page, in case you don't want to read double!)  Lately there hasn't been much to update.  He is still picky as ever and not much has changed about his diet.  He has finally had a little growth spurt, after remaining the same size for about a year, so I think his diet needs might change a bit soon.  He transitioned well from his PKU formula for infants and toddlers, Phenex-1, to the adult formula, Phenex-2.  He did not give me any problem about drinking it, and right now he still wants it and asks for it all the time.    I also know that if his taste for it ever changes, there are so many options out there now for him to choose.

He still only eats bananas and applesauce for fruits, and broccoli and cauliflower are his only veggies.  He likes tomato sauce, so he eats lots of pasta with sauce and I even made alphabet soup.  Pasta serves as a great facilitator for new food tries (as does lopro rice).  I made pesto sauce and he loved that; I also make stroganoff from time to time, mushroom soup by itself on the pasta or rice, lopro mac and cheese, or veggie broth (I don't think he was crazy about that last time).  He loves his bread now, thank goodness, and will eat a sandwich any time (lopro grilled cheese or Biscoff spread), plus I make rolls and breadsticks out of it for him to have with meals, especially when we eat rolls too.  He eats homemade lopro chocolate chip cookies every day.  It's a struggle to keep those baked!  That's his favorite!  And for breakfast, his no-fail Chocolate Cheerios!  Or sometimes lopro pancakes...

For a while he would eat blueberry muffins, but this last batch has been allowed to ferment.  He refused to eat them after just one bite.  And so we continue with the normal frustrations of a young child and his picky eating habits...just with a special diet.

His current weaknesses, or higher phe foods that could cause him trouble in the future, are Mexican food and potato chips.  We have a fave Mexican restaurant in our town, Buena Vista (shout out!), where he loves to eat tortilla chips with salsa, and a side of Mexican rice.  He also loves potato chips, and occasionally is allowed to eat tater tots or hash browns.  These are the only forms of potato he likes!  I guess we should be thankful!  On those days, we just have to figure something low in phe he can eat to make sure he doesn't get too much.

We are very blessed, though, that he does not seem to mind right now if we are eating something different from him.  I try to downplay the fact that Maggie eats the same things we do by being very discrete.  I have noticed that Carson watches on occasion, but he has yet to react or say anything about it.  We have tried to never make a big deal out of it, and our rule has always been "no eating off each others' plates".  If I have something Carson can eat, I put it on his plate myself, I do not let him reach onto my plate, so I do the same thing with Maggie.  It still works...so far.  Maggie has come along to shake things up now! 

To see what products we currently like to use, as well as an embedded link to find low protein foods, click on my PKU tab above. 

Happy PKU Awareness Month!  Don't forget to Share the Love!