Friday, July 30, 2010

D-Feast Friday --- A Review

I really don't have any recipes to contribute because I don't know the carb counts of most of the things we eat.  We just kind of wing it around here . . . 

But . . .I did have a chance to make Lorraine's Special Fried Rice last weekend and it was pretty fabulous!

Jim and I both went back for seconds. 

Ok, so my pictures are not as pretty as Lorraine's but here is my attempt at pictures of our Chicken Fried Rice -

Chopping Broccoli (& other yumminess)

The Final Product

Looks Good!!


Most Important - Nate Loved It!!

Our family gave it 4 Thumbs Up - Emma was our lone hold out only because as she put it "broccoli makes me gag!".  Ehhh - I'll leave the broccoli out of hers next time for the 5 Thumbs Up!
Thursday, July 29, 2010

A picture is worth 1000 words . . .



Last week I was asked to take part in study being conducted by Schlesinger and Associates.  They were looking for caregivers of children with diabetes (CWD).  Hey - that's me!  I have a CWD so I was more than happy to participate.

They asked me to make a collage about diabetes and bring it to the meeting.  So, the above picture is what I made and took into the meeting. Pretty cute - no?  I mean if you have to make a picture about diabetes - it's pretty cute.  Oh wait - maybe it's just my adorable son, Nate that makes it so cute!!  :)

Anyway, I have no idea who or what the research was for but I hope that I was able to help in some way because ONE DAY I WOULD LOVE TO SAY THAT MY SON USED TO HAVE DIABETES!
Tuesday, July 27, 2010

As promised . . .



and for Lorraine . . . 



Seriously, thank you all for your words of support and encouraging comments.  I let it all out and am feeling much better today.  And . . . I am very pleased to announce that after my grandmother prayed a good, long prayer for me she has forgiven me for saying BULLSHIT in my blog  - - - and I could not be happier!  :)

For all the new peeps that commented on this post --- thank you - thank you - thank you.  After a good nights sleep tonight I fully intend on stopping by your blogs and show you the same amount of love you showed me today,  Thanks again!!
Monday, July 26, 2010

Why I Still Cry . . .

Last week we (The Houston Five + Poppa DeJulius) attended the JDRF Walk to Cure Diabetes Kick Off Dinner. I promised myself - no crying!  Dang!  As soon as the Nick Jonas video started playing - I was CRYING! [Click HERE to see video]

And then again when all of these young children were on stage . . .
Lots of Cute T1 Peeps you may know in this picture.

 We have Elise from Death of a Pancreas , Liam from Sticking it to Diabetes , and Miss J and Miss G from 2 Green Eyed Girls (& their daddy too)


Look at these cuties. . .
Liam, Elise and Nate

Why do I still cry and get so emotional when discussing diabetes? Why?
I have friends and family members that have had T1 for years and are totally fine.  I read blogs written by men and women that have had T1 for as long as they can remember and they are living happy, healthy, and successful lives.  So, WHY do I CRY?

Well, sit down just a spell and let me tell you why -


Because diabetes SUCKS.  That's right I said it - it sucks.

Sometimes I wonder if I cry more for me or for Nate?  Well, some days I think I do cry for me and some days I cry for Nate.

On September 17th of 2009 - everything changed in my life.  Everything.

My life is hard.  Yep - I said it.  It's hard.  Not easy  --- not a lot of easy over here at the Houston house.
Sometimes I just get sad.  Sometimes I get mad.  Pretty damn mad!  Sometimes I just think - you know what?  This is bullshit!  Yep - I said bullshit.

It's BS that I have to use a lancet to cut my son's finger 12 times a day, make him bleed, so that I can test his blood glucose.  Yes, that is BS.  Nate doesn't even flinch - he's so strong and so tough and he is ONLY 2 years old.  That is BS.  If you are reading this and your 2-year old does NOT have diabetes - what do you think your child would do if you cut his finger and made him bleed even 1 time?

It's BS that a drug that smells like a big band-aid is infused into my son's body all day long and that stinky drug called insulin keeps him alive.  It's BS that if I make just 1 tiny mistake with that insulin pumping through his body - he could DIE.  See what I mean -  total BS!

It's BS that I NEVER sleep.  Seriously - Never!  Anyone that knows me well knows that is not a good thing.  It is my job to keep my son alive and it is a 24/7 job.

It's BS when people ask me - - - 'Why are you still checking him at night?' or 'When will you be able to stop checking him all night?'.  I want to ask them when they would stop?!?!  Would that be rude?  If your child had a disease that could potentially kill them - when would you stop checking?


It's BS when people tell me --- Oh, my cousin's brother's son was diagnosed with T1 a couple of years ago.  They're fine.  Everything is fine.  They have it totally under control.  OK - calling BS on that.  First of all if you tell me 'they have it under control' then you have no idea what the heck you are talking about.  A person with diabetes can have good control but there is NO such thing as total control. Everything is a roller coaster with T1 especially with children.  Another big fat BS when you tell me that 'they are fine'.  Really? You know that for a fact?  Or do you just assume because everything looks ok from the outside that everything is fine?  I can pretty much GUARANTEE that everything is not fine on the inside --- I don't care how long it's been since the diagnosis there are still good days and bad days.  I can GUARANTEE that every mom of a T1 still cries every now and then ---- if she doesn't then there is something wrong!!

It's BS that I am begging people for money to support the JDRF because MY son has diabetes.  It's BS because I am asking (begging) my friends and my family to walk with us, support us and donate but I feel like I'm asking strangers. It's BS because I never see my friends anymore and when I do I'm sure they are sick and tired of me and my tired ass begging them to support MY cause.  But what is NOT BS is that my son needs a cure and that is why I will keep begging anyone and everyone to help.

It's BS that I miss my normal, boring life.  I miss my friends.  I miss girls night out.  I miss hanging out and chatting with other moms.  Even when I try to do these things my brain is such mush from all of the numbers swirling around and the lack of sleep I feel like I'm not really there.

It's BS that I have to weigh, measure and count every little thing that goes into Nate's mouth.  Seriously - it is SO much harder than it sounds.

It's BS that I cannot get insurance for my children.  Yes, I know there are options out there but the options are BS.

It's BS that my 6 year old asked me the following question "Mom, if Nate has diabetes and Sophie has Crohn's --- what am I going to get?".  That is BS.



Here's why I still cry - - - because when I look at my son he looks so healthy and beautiful but I know that his BG jumping all over the place. I know that that 325 that I saw on the meter this morning is BAD!   It's really bad.  I know that his life expectancy is shorter than you son's life expectancy --- what mom doesn't cry about that?  A child's mortality is something a parent should NEVER have to think about and yet I think about it every day.

I cry because I want a cure so bad that I can almost taste it and yet somehow I won't allow myself to think about it.

I cry because I want to take this stupid disease away from my son --- I just want to grab it and take it away.

I cry because type 1 diabetes is so misunderstood and I want to tell the world all about it but when I try to discuss it all I can do is CRY.

That is all.
Tomorrow I will be back to sunshine and rainbows.
Friday, July 23, 2010

JDRF Car Magnets


I LOVE these magnets and I love that all of the proceeds go to JDRF.  My awesome D-Mom pal, Jill over at Diabetes Sweeties sent me one for Christmas and my mom was green with envy.  She was on a mission to find one for her truck!!  Now I am normally the more internet savvy one but I have to hand to to my mom --- she searched high and low and finally found the site that sells them.

You can order them at:

http://juvenilediabetesmagnets.homestead.com/

Christi and her mom, Laura (awesome name) will hook you up!!


I'm so glad she did because now our trucks look like this:

GaGa's Truck


My truck
Thursday, July 22, 2010

D-Feast Friday

FAIL. 

I am super excited about D-Feast Friday and I am super sad that I am not participating.  Here's the deal - - -
I've been sick all week, I've got the diabetes blues and I am pretty sure there is not a recipe that I can offer that doesn't spike Nate's bg to the MOON! Even the bacon and eggs he had this morning sent him off the charts - - - I give up!

Maybe he's getting sick - I don't think so.  Maybe he's growing - could be!  Maybe diabetes sucks - yep I think that's it!! 

I am already seeing fantastic recipes popping up on my blog roll so please take a look on the left hand side of my blog and check out all of the awesome bloggers that are participating!

Thank you Karen, Lorraine and Elizabeth for coming up with D-Feast Friday - you girls are AMAZING!!
Sunday, July 18, 2010

Dear Insurance Companies,

How can you not insure these 2 adorable children?


That is all.

Thank you,

Laura Houston

Just a Mom

I am NOT a doctor, nor do I play one on this blog.

I AM a wife.
I AM the mom of 3 wonderful children.
I AM my son's pancreas.

The information provided on this blog is from our personal experiences with Type 1 diabetes. Because something works for us does not mean it will work for you.

Please consult your doctor if you have any questions or concerns about your health care options.

Powered by Blogger.

Grab my button!




Check out these AWESOME
D-rent Blogs . . .
Life For A Child Button 2
o6e3vl
BlogWithIntegrity.com

Followers


D Tales

My Blog List

Search This Blog

Button
My Diabetic Child

Subscribe via email

Enter your email address:

Delivered by FeedBurner

asweetgrace" />

Subscribe Now: standard