Friday, November 15, 2013

So I am obviously totally horrible at keeping up with all these daily things.. which is why I don't do the Facebook Thankful posts or 365 in 365 days. Anyway, here's what I have for the pic a day--

Day 5: Advocate


  It's hard to see, but I have a T1D license plate and the green shoe is JDRF. Plus there's a ribbon on the driver's side of the car.


Day 6: Relationship

 Family!

 

Day 7: Blue


Day 8: Organization
Organization? In our life?? HA. Instead I'll give you this -


Walking organized in a parking lot?
(L to R - Olliver, my dad, Charlie, my nephew, Brandon and Emi)

Day 9: Support

Who better to support you than your dad?


Day 10: Exercise
Soccer!

Day 11: Play


Day 12: Work
When you're 4.5, making lemonade IS work!

Day 13: Awareness

 I'm stretching here, I know :P


Day 14: WDD


This was the kids yesterday on World Diabetes Day. They were with Mamo (Maggie Duncan) who took this picture after they made hats!

Day 15: Aler

Ollie with his Blood Sugar Fairy and you can see his Alert bracelet. That's the best I got!

And I'm caught up.. for 3 more hours :P



Wednesday, November 13, 2013

Olliver's 4 year Interview

1. What is your favorite color? "maybe all the colors. no purple"
2. What is your favorite toy? Blocks
3. What is your favorite fruit? strawberries and oranges
4. What is your favorite tv show? Jake and the Neverland Pirates
5. What is your favorite thing to eat for lunch?
6. What is your favorite outfit? Batman shirt
7. What is your favorite game? Angry Birds
8. What is your favorite snack? Apples
9. What is your favorite animal? Dee
10. What is your favorite song? "Old Mc Donald had a farm"
11. What is your favorite book? Curious George
12. Who is your best friend? Dee
13. What is your favorite cereal? Square cereal (Quaker oatmeal squares)
14. What is your favorite thing to do outside? my new basketball and hoop
15. What is your favorite drink? Chocolate milk and white milk
16. What is your favorite holiday? .Halloween
17. What do you like to take to bed with you at night? Dee
18. What is your favorite thing to eat for breakfast? chocolate chip muffins
19. What do you want for dinner on your birthday? Melting Pot
20. What do you want to be when you grow up? "I don't know"
 
5 year:
1. What is your favorite color? Green
2. What is your favorite toy? a toy plane from Disney World
3. What is your favorite fruit? bananas
4. What is your favorite tv show? Ghost Hunters
5. What is your favorite thing to eat for lunch? shrimp
6. What is your favorite outfit? button shirts (button up) and his red tie shirt
7. What is your favorite game? hide and seek
8. What is your favorite snack? Angry Bird graham crackers
9. What is your favorite animal? giraffes
10. What is your favorite song? Christmas songs
11. What is your favorite book? bug book
12. Who is your best friend? Brandon
13. What is your favorite cereal? Honey nut Cheerios
14. What is your favorite thing to do outside? Basketball
15. What is your favorite drink? fruit punch (Crystal Light)
16. What is your favorite holiday? Christmas
17. What do you like to take to bed with you at night? Dee
18. What is your favorite thing to eat for breakfast? toast with jelly
19. What is your favorite dinner? mac and cheese and carrots at MeMaw's
20. What do you want to be when you grow up? a Batman
 

Monday, November 4, 2013






 Day 1: Past (11/12)






Day 2: Checks (Yep. Low. At night).



Day 3: Snacks (who doesn't love ice cream??)




Day 4: Proud (Checking his own BS)


Thursday, October 31, 2013

Diabetes Awareness Month!



Also, November is Diabetes Awareness Month. I plan on being highly annoying on my Facebook page and hope to continue the trend on here. Seriously though, text the number and get texts through out the day telling you to "check" your blood sugar (the rubber band snap. Not the same pain, but I guess it's feasible).

Happy Halloween!

Happy Halloween from our bat and Princess Sofia the first. 

How does a diabetic do Halloween?


I dunno, how does your kid? Yep. Mine too ;) Ollie was content to have 2 pieces of candy tonight after Trick or Treating.. he picked them out himself and got a Reese Cup (kid after my own heart) and a bag of Cheetos. <3 He had no issues with knowing he wouldn't eat everything tonight (we wouldn't have let him even before T1D diagnosis). I thought it was sweet that Doug put both kids in their JDRF walk tshirts to go to sleep in :)

Ollie also had his 5th birthday last week. 

I can't believe that he's 5! It seems like that those pics on the bottom were just taken (2yrs, 3 and 2.5 in order)! He had an amazing day at Chuck E Cheese and his joint party (my nephew's birthday was yesterday, so we're having a joint party) is this weekend. He is so excited :D I love seeing experiences through the eyes of a kid. And no matter what, he's a kid first, diabetic second. I've recently found a group on Facebook that's amazing (if you're a T1D parent, shoot me a message and I can add you!) and it's nice to keep getting that reminder.

Wednesday, September 18, 2013

JDRF Walk for a Cure

Sunday was our JDRF walk. I am SO pleased to announce we raised $437!! It was a very busy and packed event. We got there early enough to walk around before the walk. We saw different pump sponsors, food booths (with carb counts listed!), games, bounce houses, an awesome band playing and TONS of people. We weren't really able to connect with anyone in particular, but I want to connect with some local D families.

Yesterday, my sister, nephew, Emi and Ollie and I went to the Smith Aquatic Center in Charlottesville. First of all, um, AWESOME place for little kids. Probably not so great for like, 7 and over. Second, Ollie was checking his BS in the locker room (yep, he's started doing it all by himself!) and a mom walked by and said "my little girl does that too" - she has an 8 year old whose been dx'ed with T1D for 6 years. It was nice to connect with another D mom even if only for a few minutes! 

Monday, September 9, 2013

JDRF Walk

Isn't it weird how things we acknowledged before now are in the forefront of our lives? I vaguely heard about the JDRF walks, saw the Diabetes support shoes and hands at Subway and other places.. now it's my life (although, by some weird work of fate, I've actually only tested Ollie's BS once in the last 48 hours!).

I'm really getting excited for our JDRF walk this weekend. I really hope Ollie enjoys it and can make a connection that he isn't the only one who has Diabetes. (Note to self: Start fundraising earlier in the year! Like, next month!)

Donate to The O-Team!


Monday, September 2, 2013

6 month Diaversary

So, we can officially say we survived 6 months of Diabetes.... 6 months?? It seems like a lifetime. I can't remember the last time I looked at food and didn't think about carb counts. I can't remember not worrying about ketones and highs, or lows. To to top it all off, Ollie now has a cavity (my theory is from correcting lows at night). These past six months (again, are we sure it's ONLY been 6 months??) have been a whirlwind of math, emotions and needles. Ollie has proven time and time again to be an amazing trooper through all of this. I can't imagine what he goes through - not only the testing and insulin, but the highs and lows. I've read that coming down from a high can make you feel sluggish and sick. The many times as he's gone high (or low) and come back in to range, I always try to let him relax, but there is no slowing him down.



Last week I signed us up for the local (well, most local to us) JDRF walk. I can't wait for Ollie to be around other T1D kids! I would love to find more local (like, really local, not an hour and a half away) kids and parents for us to be around, but I figure this is a start. Anyway, if you have the time, or resources, we would all love for you to check our page out - any step to curing Type 1 Diabetes is amazing to me.

The O Team (JDRF Walk)

Wednesday, July 17, 2013

Flying!



We had a great experience flying to Portland. As you can tell from the picture, Ollie was thoroughly amazed. (You can also see hubby's T1D tattoo on his wrist in the 2nd pic).Only kidding, he did enjoy it. He and Doug sat together for the first leg and played games and watched the inflight movie. Emi slept beside me. (These pics were taken 2nd leg- LAX to PDX). We switched kids on the next flight and that's when Ollie fell asleep... Beside me! I must have that effect. (In my defense, they had woken up at 5am, way earlier than usual!) We had no issues with his T1D supplies. The TSA agent at Dulles didn't even bat an eye. The only problem we had was the ice pack didn't stay cold as long as we needed for his new/extra meds and they got warm :/ On the way home, I forgot to tell them what the bag was/had in it, and not one word was said. Seriously, we had more issues with the kids car seats than we did his supplies. Anyway, we did touristy things in Oregon- (Tillamook Cheese Factory)
 attended a wedding (the reason for going out!), 

hung out at the beach house with family and friends
 played on the beach,
Had a bonfire,
(That's my cousin, Andrea- it was her wedding! I hope she doesn't mind this picture of her talking ..)

Moral of the story: don't fear flying or traveling!! We took more supplies than we ever needed, but felt better about traveling. We were prepared with a letter from the Endo but didn't need it. Oh, his sugars were so wacky, (I think due to time change/meal difference) but we just went with the flow. Next time I will come up with a better solution for new, unopened meds.

We had an amazing time! I wish Andrea and April the most amazing life together :)  thanks for sharing your special day with us!!

Monday, July 15, 2013

I'm ecstatic that I got this in the mail -





This was the most challenging semester for me yet. We started clinicals, I missed a week because of DS's T1D diagnosis, and we had a bunch of ups and downs, yet I still had the energy, the time, the drive and the support (especially from my amazing husband and family!) to get on the Dean's List. It may have been by the skin of my teeth, but I did it :)

(If anyone doesn't know, it's for Respiratory Therapy, by the way!)

Tuesday, June 25, 2013

Yay!

Hey! There's an app for that.... Blogger mobile!!

A1C, the Pool and Vacation

First A1C -
What is A1C? It's a blood level that kind of gives a picture of how blood sugars have been for the past several months. When Ollie was diagnosed, it was over 10. At his first appointment it was 9 something. At his appointment this month, it was 6.6! I've always heard under 7 is great... however, that isn't for a preschooler. It's too low.. who would have thought?? His goal is 7.5-8. He's apparently having lows at night. Have you ever attempted to wake up a sleeping child to force feed them candy or chocolate milk?? No?? Yeah, me either until this year :P

This was Ollie being forced to eat a Starburst. The rest of his appointment went well, however. No changes to his doses or anything.

Next up - the pool.


Any summer activity is a challenge for glucose levels. Happily, he seems to be doing well. We spend a decent amount of time in the water. Yesterday, it thundered (boo!) while we were there and if you've ever been to a public pool you know you have to get out for 15 or so minutes to make sure it doesn't storm. We (we met 2 of my BFFs and their kids there) decided to wait it out and went over to the playground beside it. There was another little boy playing, who I guess asked Ollie about his bracelet. Ollie, being the champ he is said "Oh, it's my bracelet. I can't take it off. I'm diabetes" Well, close kid. Good enough to make this momma proud. I think the kid moved on and didn't question him anymore.

Lastly, vacation. I'm so glad for all my new D friends who have given me so many links and information about traveling. Here's to hoping the Dulles TSA agents don't question us (most people have said they have no issues, possibly a swab of meds to make sure they don't give off a toxic substance or something?) and Ollie holds ok on the plane. We're flying to IAD to LAX, then to PDX (for those non flying people [which I am one of you, I'm just pretending to be in the know because I know these acronyms ;)] that's Dulles (Wash DC) to Los Angeles,CA to Portland, OR). The first flight is the one I'm worried about, because it's the longest at about 5 hours. Thankfully I found out we can take food past security, just not liquid (although, because of the D we probably could, but I don't want to chance it and we CAN buy drinks. It's not a necessity for lows, we have options.) I'm planning on taking several snacks for each kid, along with new activities.

Now, just pray for my sanity and upper arm strength through the airport.

Tuesday, May 7, 2013

Two months already?!

I missed our 2 month anniversary (which was 4/22)

Eh, not a day I really want to remember over and over anyway! However, looking at it differently - we have survived 2 months! 2 months? It feels like a lifetime. It feels like 2 years some days. I'm starting to feel like an old hat "Oh, you want shrimp, ok, if you take the breading off like normal, it's about 2-3 carbs" (Allowing for leftover breading on them). "Oh, you want a PBJ? 26 for the bread, 3 for the jelly, 5ish for the PB". Then other days he eats a donut and ends up sky high. The doctors and nurses said we'd get it. We'd just become carb counting experts and 'know' it. I laughed - remember MORE numbers? Ha! But they were right. It did come, we did realize what to do and how to do it and when to panic and when to relax. Now, if only I could find the missing medic alert necklace I'd be feeling better!



Switching gears...here's some facts about Type 1 Diabetes:
It is NOT caused by what you eat.
It is NOT preventable.
It IS autoimmune - your body attacks itself for a reason that is unknown.
Insulin is NOT a cure - it's a treatment until a cure can be found.

Please think twice before 1) asking if a diabetic can eat something and 2) saying that your sugary treat is going to cause you diabetes. I've only been confronted by these a few times, and normally it's not hateful. But really, don't think that witholding that cupcake from your kid is going to prevent diabetes. Heck- Ollie ate a cake ball earlier today!

Sunday, April 21, 2013

Some days are frustrating. Well, a lot of days are frustrating, but when you have a kid with T1D, it's a different kind of frustrating. I worked today, but his numbers this morning looked something like this - Waking, 60. After breakfast, 310. Before lunch, 67, Before dinner, 217. After dinner 69. Whaaaaat??? Imagine the above. So, he bounced between that and feeling crazy off the hook from being high ALL DAY. Back and forth.. screeching about whatever - it's never a normal voice -and then imagine not being able to figure out WHY - Is it the carb count? Is it the overage factor? Is it what he ate? Should he eat something else? Life is hectic enough with 2 kids, school, work, Doug's work, but now we have to second guess EVERY.THING. it seems.

Monday, April 1, 2013

Happy Easter!

A week after Easter 2012:

Yep, chugging chocolate milk.

Easter 2013:
Yep, runny nose, bunny hat and all (I'm sure I'll pick on him years from now for this). Do you know what I find amazing? We got a handful of candy for Easter and that's it. Normally we'd have a  TON - in eggs, in baskets, all over. This year, Doug and I got some Starburst (which is Ollie's preference for when he's low.. so yes, I kind of cheated and he got "medicine" for Easter :P Ha!), a family friend got him some sugar free candy and then a friend of mine got him some diabetic bars and sugar free candy. I am so happy with how people have adapted and thought of him. That is seriously what gets me - not the fact we have to deal with diabetes or shots or glucose checks - the fact that people are all thinking of him and keeping us in mind and not making it so I have to be stuck explaining why he can't have something someone gave him. (Geez, did that make any sense?)

So, what do you DO for Easter that doesn't include tons of sugar??? In their baskets the kids (from us, err the Bunny) got Matchbox cars, an Angry Bird pencil kit, 2 snack bags each from my friend's store 6 Silly Monkeys, a small notebook for each, bubbles, playdoh, and Ollie's big present was an Iron Man mining vehicle. As for the eggs- the Starburst were in there, yogurt covered raisins, pistachios, finger flashlights, coins, some cars for Ollie and binkies and nailpolish for Emi.

Surprisingly enough, after breakfast (eggs, cinnamon rolls made from crescents and a couple Starburst thrown in there) he was LOW. Say whaaaaat? I'm glad he had those Starburst, who knows how low he would have been without them!

Anyway, I'm happy to say we conquered our first T1D holiday!

Oh, and a bit of advice? When someone tells you their child has Diabetes 1) don't assume it can be fixed by diet. and 2) DO NOT tell them about your great aunt's boyfriend's daughter's mother in law who had to have a kidney donated to them and then lost a leg or eyesight or whatever. Seriously, just don't do it, ok? KThanks.


Monday, March 18, 2013

Sometimes I don't know how much information people want. However, tonight, I realize it doesn't matter. It's the amount of information people NEED. Is it scary to give your child (or grandchild or nephew ) shots? Yes. You don't want to hurt them.

But you know what? A friend I've had for 5 years (We met on a November 08 birth board online - her son and mine actually share a birthday!) is with her son at their local children's hospital because of new onset Type 1 Diabetes. She realized it due to me posting Ollie's symptoms. So yeah, it's what people NEED to know, not want.

Sunday, March 17, 2013

Clockwise from the top, Brandon (my nephew, 4), Emi and Ollie playing at my parent's house this weekend.

Staycation 2013

This past week Doug took off for my Spring Break. We didn't go anywhere overnight, just stayed home.

Well, as much as our family stays home. You'll soon learn (if you haven't already) that we're an On The Go Family. Monday we went to the Massanutten Water Park (although, looking at the link it says it's always 84 in there, um, I was cold!). The kids had a blast in the "Crazy River" (ie, Lazy River" and we LOVED that it had double tubes where one had a bottom the kids could sit in! SO much better than other places we've been where we've had to finagle the kids on our laps or hold them on the tube. 10000 Thumbs up on that, Massanutten!! Ollie did a bunch of slides on his own, both kids loved swimming in the pool area. We can't wait to go back this summer! Too bad it won't be as un-crowded as it was last week - there was minimal waiting for everything except the big adult tube slides! What, you thought Diabetes would slow us down? Heck no!

Wednesday was our first Endocrine follow up appointment. The day started with us having to wake him up early (bad juju 1), him not eat all of his breakfast (bad juju 2) and him fall asleep during the appointment (actually not bad). His BS was 125 (even without eating all his cereal!) and his A1C was 10.4 - I was mistakenly told 9.8 in the hospital it was actually 11.8 - sliiiight difference, eh?? We were told we're doing excellently with pretty much everything. The dietician was happily surprised to see we have a log book of everything he's eaten since he was diagnosed (although, this week it hasn't been 100% accurate, oops). The attending Dr was nice, although he told us to not give him so many cheese sticks after the initial period.. I'm still scratching my head over that one.  Good news: We were told that if Ollie's numbers continue to be normal over night we can drop at least one check soon! They were going to tell us to drop one at the appointment, but he'd been having some lows overnight that week. We changed his dinner carb ratio and his Lantus dose. We also got a Lantus pen (instead of a vial of meds with a syringe). It has its pros and cons - pros, it's more accurate dosing, it's easy to use, nice to have 2 different systems (the Humalog is still vial/syringe) so they don't get confused, you can't get bubbles in it. Cons, however - it can't do half units and there's some leak back we're dealing with (leak back is when you pull the needle out, there's a bubble of med on the skin, so he didn't get the whole dose). All in all, I really like it! I wish we could have both be pens, but we really need the half unit of Humalog right now.

The rest of the week was quieter (well, minus Emi chirping "Wadoo pack??"[water park?] every once in a while. Happily, we correctly bolused for a breakfast buffet, pizza and a piece of cake. No, that wasn't one meal :P Olliver is starting to slow down on eating. He's starting to not scarf everything on his plate and then some. He's also not always begging for snacks right after a meal. Doug and I were talking yesterday - we're both getting better at being able to tell when his sugar is out of whack. We've had several lows this week - and Ollie can tell, too. He's pretty good at telling us to check his finger, or ask for his "green bag" (his meter and supplies are in a camo type bag).

I know I've said it before, and I'm sure I'll say it again.. however, Ollie is doing amazing. We tested sugar at the water park, we gave an injection in Panera, we tested his sugar in the car... he hardly complains (especially for a cranky 4 yr old who doesn't know really what's going on!). I know it sucks for him, it does for all of us! But we're getting a routine (he likes to use the alcohol wipe himself, pick where we're injecting/testing, he likes to check the needle to make sure it's there, he likes to see the medicine in the syringe, etc) and it's working.

Tuesday, March 5, 2013

12 days later....

12 days later.. people might assume it's all gravy now, huh?

Nope.

Diabetes is an asshole. Sorry, that's the best word I can think of. It sneaks in and takes my precious boy and turns him into a lunatic. Screaming that he's hungry. Crying he doesn't want "his leg" (ie insulin). Whining in general. It's amazing to be able to step back and see him having a tantrum and now go "Oh, yep. He's high" (and I mean that in the best way possible. Although, this way sucks too.. and he has no control over it).

The good part is we ARE getting used to it. We now know we DO NOT leave the house without the insulin, even if we're just running to the store. You never know if it'll take longer than you expect and you need to grab lunch (or, you know, if you're looking at car lots for cars and your kid will see Red Lobster and beg to eat there, you get out of the car, look at your husband and both say "You grabbed the insulin, right?" and have to get BACK in the car to drive home to get it. You know. Hypothetically).  We've also learned that Zinga has a no sugar added vanilla (Ollie's favorite) that has 16g of carbs for about a 1/2 cup. Everyone keeps telling me ice cream is a great bed time snack, so why not? ;)

Want to know the rest of the list of stuff we can't leave without? Blood monitor, test strips, lancets, "pokey thing" (the needle), cotton balls, band aids (several types so he can pick), log book, pen, syringes, alcohol wipes, low fat cheese sticks, no sugar added Jello, several 15g snacks (Cheerios, nuts, Teddy Grahams, etc), juice boxes (in case of a low), sippies with water, Glucagon pen, Ketone strips and the Calorie King book that gives us nutritional info on places we eat. Oh, plus Little Sister's diapers, wet bag, extra clothes and binkies. Yep. Never complain about a regular diaper bag again!

One of my lessons for "non T1D" folk: The next time you see a mom with a kid, and the kid is a screaming, crying brat.. think twice before you think the kid IS a brat. There could be a multitude of issues that could be causing it.

Wednesday, February 27, 2013

3AM

My alarm goes off - 3AM. Doug and I roll out of bed, get the meter and everything together, I put on the headlight (yes, we wear an oh, so fashionable flashlight headlamp. It was actually a kind of gag gift for Doug for Christmas!). I poke Ollie's finger - great drop of blood first try! The meter reads it (287 if you were wondering), we get everything put away in probably under 5 minutes! I'm reaching for the sharps box and .... Drop the lancet. We're talking a tiny little semi clear/light blue thing on our white bathroom floor.

It's still missing. Be careful if you go into my bathroom.

Monday, February 25, 2013

Totally Not Current Normal New Normal

I'm not an idiot. I like to think of myself as a fairly educated person. Add on to that the facts that I've worked in an Emergency Room (as a secretary, but you pick up on a lot being in an environment like that) and I'm in a Respiratory Therapy program, I have a good portion of medical knowledge.

That being said, when I took my son to the pediatrician on Friday 2/22/13, for what I assumed to be a stomach bug, maybe the flu, worst case scenario appendicitis (Olliver had been complaining on and off of stomach pain for a week or so, had been throwing up and very lethargic for 2 days) and the pediatrician had a nurse come check his blood sugar - my brain was confused. Blood sugar? Why would that be an issue? I guess he's just checking it for a baseline to rule it out.  When the meter read 544 - my brain went even FASTER. WHY is it so high? Dr M came back in and could read my face - I knew that was super high. Like, holy crap high. He told me that Ollie has diabetes and is in DKA. All of a sudden the past couple weeks made sense. Olliver had started drinking tons of water and peeing more. I figured this was just good habits. He had been eating more - I figured a growth spurt. Ollie had been getting SUPER cranky before meals (which I now know is his blood sugar peeking). His "tummy bug" was actually DKA. We were sent to the Pediatric ER and told to expect to stay in the PICU. I came home, grabbed some stuff, picked up Doug and Emi - dropped Emi off at my in-laws and raced over the mountain. We were taken back immediatly where his Accucheck read "Hi" (Yep, hi to you too, Meter but I don't feel like chatting right now. Kthanksbye). Ollie got a line placed and barely whimpered. We were admitted to the Pediatric Intensive Care Unit with a blood sugar of about 500. He was a picture perfect patient, no screaming, no complaining. The worst part of the night was that Ollie was NPO - he wanted water but we couldn't let him. The Pediatric Endocrine Fellow came and spent a good amount of time talking to me. Friday night we had nurses coming in hourly for accuchecks and they did labs several times overnight as well. Ollie slept through all of this. I however slept about 3 hours.
Saturday morning, Ollie was allowed to eat.. and not happy. We now have to carb count his food out and dose him with insulin according to how many carbs he has. Thank goodness I had purchased Amazon Prime for the streaming videos for him. It was seriously a lifesaver! Saturday was a whirlwind of a day - doctors, nutritionists, family.. lots of people in and out of the room. We met the Pediatric Endocrinology attending, who said we'd probably go home on Monday best case scenario. We were moved to a regular room in the evening and Ollie got a wagon ride out of there -

On the regular pediatric unit, we had to share a room. Ollie got his bedtime snack, accucheck and insulin and we both fell asleep around 9:30. Somehow, I slept through the midnight check (as did he!).

Sunday started out cranky. Ollie wanted his food, which wasn't coming up quick enough for him. We had an AMAZING nurse, Kelly. He got his breakfast, was eating and FINALLY had to poop (it had been days, seriously). When we came back from the bathroom... the breakfast tray was gone. The very efficient tray lady had picked it up. Which, while normally would make a pre-schooler cranky... this one NEEDS his carbs because we dose his insulin depending on how many he's going to eat. He had only eaten about half so um, PANIC MOM. I gave him an extra carton of milk, some grapes and called the nurse. She said I did exactly the right thing and brought a pack of graham crackers as well. Dr L (the Fellow) came back in and said again, I had done the right thing. I was starting to think I might get the hang of this, finally! Dr C threw us a curve ball and asked if we'd like to go home after lunch if we felt comfortable - um, YES! Ollie's after lunch numbers were high, so I had a momentary defeated feeling, but they let us go home because that was kind of normal for him at that point and we felt comfortable treating it.

And away we went!

To answer questions that I'm sure are out there : Yes, we have to give him insulin - 4x a day. Before each meal and before bed. Yes, we give him accuchecks 9x a day. Before each meal, 2 hours after a meal, at bedtime, midnight and 3am. Yes, he can pretty much eat anything anyone else does... as soon as I figure out how to carb count it!