Dear Coach …. please keep my kid alive

It’s that time of year again…

Basketball season 💗🏀😳

 

I have a LOVE/HATE relationship with it… mostly LOVE…

I LOVE the game – and even more so, I LOVE watching my girl play the game, do what she does best and loves with all her heart.

 

But – I HATE it because it causes me stress .. lots of stress

 

This year is the first year Eden will play basketball for her school – she has played other sports – but basketball is just different.. it impacts her body differently and I KNOW my child will NOT stop, take a break, check her blood sugar or sit out for one minute if she doesn’t have to, because she loves the game so much.

 

Eden had her first official “tryout/practice” yesterday.. I made all the previous arrangements with the school to be sure the new coach would be sufficiently glucagon trained for a Type 1 Diabetes emergency – which was done right before the session.

At the end of practice I approached him and introduced myself and said I was “Eden’s mom” …

his response – WHICH one is Eden?

Yup – slight internal FREAK OUT from me.. In my head – you mean, the emergency training you just had and the kid you just learned has a life threatening condition and are supposed to ensure is SAFE and you don’t even KNOW WHO SHE IS ?!?!

 

Calm down – momma bear.. calm down…

 

Resume conversation – question him on glucagon training to ensure it took place – get a very off hand – “oh yea, the insulin thing” response..  I’m sure I had a look of pure horror on my face ..

 

I honestly can’t even remember exactly how the conversation went from there – I probably rambled – he had a deer in headlights look – and I handed him my cell phone number and email address and said I would send him additional information and guidelines that needed to be followed..

 

Yes – Eden is in Middle School and for the most part can manage the majority of her T1D care.. I’m SURE I sounded like an over bearing, over protective momma – BUT – exercise is a different animal all together – basketball is different – AND I KNOW MY KID…  and I am entrusting a COMPLETE stranger – who clearly knows nothing about her medical condition – or even what she looks like to keep her SAFE..

 

… insert major stress here … 😳

 

Type 1 Diabetes is SO unpredictable… you just NEVER know what will happen especially when exercising..

 

prime example – last night..

 

Eden has her first real “coaching job” – she was asked to be assistant coach to a 3rd/4th grade rec team.. SO EXCITING! She insisted that I didn’t need to stay and I could drop her off because she wouldn’t technically be exercising… I did think about it, but being her first time I wanted to see her in action! 😃

We had an early dinner and on the way there her blood sugar was trending low and she still had a LOT of active insulin that would lower it further… It was a fairly heavy dinner and I was pretty confident that her blood sugar would rise substantially to counteract the insulin and told her she needed to keep her insulin pump ON (she usually takes off for basketball) and did not give her any additional sugar..

As practice begins, her blood sugar starts to drop and hover at a pretty low level – within less than 30 minutes we were pulling her from the court – giving her glucose gel and taking her pump off so she wouldn’t get any additional insulin… (her Dex read BELOW 55) Because we were alerted by her CGM and watching what was happening disaster was averted. Her blood sugar was falling rapidly and Eden had NO CLUE her blood sugar was tanking…

This is what makes me SO NERVOUS – and she wasn’t even “exercising”…

 

fast forward to this morning and my “dear coach – please keep my kid alive” email below…

overboard? maybe …

necessary? I certainly think so..

I tried to keep it as concise and to the point as necessary – unless you live the T1D life – you just DO NOT realize how serious this can get and HOW QUICKLY it can get there… He needs to know it is serious .. and not just a blasé – “oh yea, the insulin thing”.

 

Yes – I need to find the strength to let go and have Eden take the reins – but as I said before – I KNOW MY KID… She has put her life in jeopardy one TOO MANY times when left in control in the past.. She is just not there yet and neither am I.

 

As discussed – below is some additional info in relation to Eden’s Type 1 Diabetes…

I am unsure exactly what Nurse XXX covered besides what to do in an emergency situation – obviously we need / want to prevent it ever getting that serious!

Type 1 Diabetes is an incurable AUTOIMMUNE condition – where her body attacked and destroyed the insulin producing cells in her pancreas. Not to be confused with Type 2 – nothing she did or didn’t do caused it and it is not due to a lack of exercise or poor eating habits. A healthy pancreas automatically secretes the appropriate amount of insulin and balances/maintains a healthy blood glucose level. Eden’s body DOES NOT produce any insulin naturally so we need to give it externally and monitor her blood sugar extremely closely 24 HOURS A DAY – EVERY DAY..

Eden wears an insulin pump to infuse her insulin and will take it off for basketball, she also wears a CGM (continuous glucose monitor) on her arm which takes a blood sugar reading every 5 minutes.

Basically a “perfect” healthy range for Eden’s blood sugar is around 100-120 .. to get it to this level and keep it there is VERY difficult and a daily struggle.

HIGH blood sugar = requires insulin
LOW blood sugar = requires sugar

Anything below 70-80 is considered “low” and bordering dangerous for basketball – exercise will usually cause her blood sugar to drop further so she needs instant sugar to bring it up to a safer level (juice / glucose tabs / fruit gummies in the box I gave you) anything lower than 70 and she should technically sit out for a few minutes and then re-test her blood sugar to be sure it is coming back up. Usually she is able to eat something quickly and get right back at it but she DOES NOT always feel her blood sugar dropping and it can happen very rapidly when exercising even if she starts at a “perfect” blood sugar level. Low blood sugar is much more immediately dangerous than high as her brain and body need the sugar to function and survive and it can be immediately life threatening. She could collapse, have a seizure and pass out if too low – thus the glucagon training you had. Her fast acting sugar and glucagon need to be readily accessible at all times.

We prefer her to be in the high 100’s for basketball – that gives her a good cushion in case she drops. Starting there – not always so easy. On the flip side – if she is 300 or over – she CANNOT participate until her blood sugar levels start to come down.

Eden will be responsible for checking her blood sugar prior to practice and notifying me. I will have her communicate that number to you – please text me – so that we can cross check and know she is good to participate.

The problem with starting to exercise when her blood sugar is elevated (250s or higher) is that it usually just continues to rise as her body then feels it is under “stress”. It isn’t immediately dangerous – but she does require insulin to bring blood sugar back into range and you may notice changes in her behavior. Unfortunately high blood sugar causes slow reaction times, a dazed, spacey look and the inability to focus. She is not being disrespectful if not following instructions – she literally cannot process what is being said and it is completely out of her control.
Eden is an extremely athletic kid and has been playing competitive basketball for many years. Type 1 Diabetes does NOT hold her back but it does require constant and diligent management. We are working really hard to try to get Eden to take responsibility for her health – but it is an extremely hard balance to maintain – and even harder when playing basketball because she DOES NOT feel blood sugar changes when she is exercising and does not want to leave the court or be a disruption.

Technically she should check her blood sugar and/or the reading on her CGM device (I attached picture so you know what I am talking about) every 30 minutes. Even keeping this device on the bench would be great – easier for her to check (and yourself if so inclined) and know where her levels are. Thankfully we have wonderful technology that enables us to also view her CGM reading remotely so we can monitor her from afar – but technology is technology and it does not always function or we lose connection.

 

Let me know if you have any questions or concerns ..

Communication will be key to keep Eden safe and ultimately have a great basketball season!

I understand that the 8th grade coach was also glucagon trained – I will have Mr XXX give him this additional information for reference also.

Please be sure to notify me if you are going to be absent from practice so we can ensure Eden will be in safe hands.

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Bacon to the rescue – just another Monday living with Type 1 Diabetes… 

 

I picked Eden up from school today and it was instant “grumpy” ..

she got in – glanced down and saw the lab paperwork in the center console and knew we were headed to get blood work.

“oh, great, blood work – really?!” ..

yup – sorry kid..

 

I asked her to check her blood sugar – the usual first thing she does as soon as she gets home from school

her response – “oh yeah – my site came out” as she shows me the end of the tubing that SHOULD be attached to her body and infusing the insulin she needs to SURVIVE..

 

huh, well that explains why her blood sugar would be in the 400’s ?!

 

I keep driving until there is a safe place to pull over and get a new infusion set out of her D bag – the kit she carries with her everywhere – and now not only is she going to get blood work, but I am having to jab her with a giant needle on the side of the road..

grumpy silence the entire drive to the lab ..

 

Once there, I WANTED to take pictures (just of her arm mind you) for the benefit of Diabetes Awareness Month, but in her current mood she was having absolutely nothing of it..

 

Blood work completed – USUALLY afterwards she gets a “treat” … maybe a Starbucks or ice cream or something small – just because getting blood work every few months is not something she enjoys but will be a part of her life forever.. in the early years it was probably a bribe and the tradition stuck.

BUT – given the fact that her blood sugar WAS NOT coming down – and the anxiety from the blood draw had actually sent it UP higher there was no possibility of a treat.. 😕

 

As a Type 1 Diabetic SHE CAN eat anything and everything…

the difference is whether or not it is a good idea.

 

At this point in time – I had to say NO.. it was much more important to get her blood sugar back in range first.

 

so now Eden had endured –

  • a new site inserted on the side of the road
  • bloodwork – 4 vials of blood drawn and a tech who “clicked the thing” as she said – and hurt her
  • me saying NO to the treat that she usually gets afterwards
  • and being STARVING and not able to eat until her blood sugar comes down a little bit.

 

 

Another example of the stuff people don’t see or realize goes on behind the scenes .. every.single.day.

and aside from being grumpy and me getting the silent treatment for an hour or so- SHE DID NOT COMPLAIN

 

 

A few hours later – her blood sugar is improving and she asked me to make her some bacon..

how could I refuse… ??

BACON TO THE RESCUE ..

Bacon requires no insulin, does not cause an immediate spike in blood sugar and is the stand in “treat” for today – at least it brought a smile to her face

 

just another Monday living with Type 1 Diabetes…

 

Oh boy… what a way to start the day

 

This is what you get when you “rage” bolus in the wee hours of the morning… a guilt producing, scary low blood sugar reading that you, the parent caused. 😢

 

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Multiple, multiple times every single day we make medical decisions that affect Eden’s life.

We do the very best we can to act like her non-functioning pancreas but we make mistakes, we are not perfect and Type 1 Diabetes is unpredictable and stupid.

 

the backstory…

Last night Eden had basketball practice – as typical LATELY – her blood sugar starts off fine and then adrenaline kicks in and she skyrockets mid practice. I have experimented with giving her extra insulin before practice to counterbalance the high that is coming – but that in itself is very risky. Exercise typically causes a DROP in blood sugar, so additional insulin upfront could have BAD consequences. Adrenaline highs usually correct themselves over a period of hours after her body recovers and her blood sugar levels out.

I say USUALLY…

Because over the past few months, everything that we had become accustomed to her body doing has changed. Her body is changing and so are her insulin needs and how it reacts.

 

We change Eden’s insulin pump site every 2-3 days.

We fill the reservoir in the pump that holds the insulin with 2-3 days worth of insulin. (mind you she doesn’t use the same amount daily) The insulin only stays stable for that length of time due to body and outside temperatures and we also need to rotate the location of the cannula under her skin. The longer the cannula stays under the skin in one place, the poorer the adsorption, the greater risk for bacteria entering her body and the development of scar tissue. The longer the insulin stays in the reservoir, the more it breaks down and is less effective in controlling her blood sugars.

Eden does not particularly like having her site changed. Honestly, I really can’t blame her – its a big needle that we have to insert into her body and I hate having to do it – but it is a necessary evil.

I mark on my calendar the 2 day mark and check in with her on how much insulin she has remaining so that she doesn’t run out, consider how stable her numbers are and go from there. Yesterday was day 3 and her site needed to be changed but she still had plenty of insulin left to get through the night after practice so I opted to put it off and do it in the morning – putting off inflicting pain on my child and wanting to use every precious drop of the liquid gold she had remaining in her pump.

 

8.40pm :

Her blood sugar after practice was high – not unusual – and not as high as it has been getting

 

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A fairly typical reading of late – she gave herself a correction dose of insulin to bring it down and I watched Dex closely over the next couple of hours.

10.30pm:

Bedtime for me and Dex showed she had come down consistently – not too quickly – and leveled off in the 200’s.. I was totally happy with that knowing that she would continue to drop on her own.

12.00am:

What I did NOT expect was at her next check that her Dexcom reading would be WAY off  – showing a reading in the mid 200’s when a finger prick was actually 395 😒

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YIKES…

SO – I give her another correction dose of insulin using her pump and stumble back to bed.

Restless – I continue to check Dex consistently over the next few hours – waiting for it to catch up and display an accurate blood sugar number. Dex still showing in the 200’s..

3.20am:

Get up again and do another finger prick… 302

UGH… another correction with her pump.

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Back to bed – I fall asleep for 30 mins or so and it dawns on me… HER PUMP SITE IS NOT WORKING.

Fed up and exhausted – I get BACK OUT OF BED – head to the supply cupboard – get a syringe – go to the fridge and get the insulin. I draw out insulin for the correction I am convinced she just didn’t receive and an extra unit to make up for the basal insulin she wasn’t going to be getting..

I take the insulin and I inject it into her arm and head back to bed.

2 hours later and I am awoken by D-dad getting up and ready for work. I look at my wrist and it says Eden’s blood sugar is 85 with an arrow down… I thought to myself – well, it probably isn’t accurate – it has been off all night – fighting the need to get up.

5.45am:

Get out of bed AGAIN to test Eden.

Finger prick 85…

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SPOT ON – COMPLETELY ACCURATE and MATCHING DEX

SAY WHAT ?!

Well, I guess my day has now officially started.. 85 is on the low end and thanks to Dex it shows, still dropping. Given the fact it is Spring Break and she will be in bed for a few more hours – too low for my liking..  Within minutes, my wrist is vibrating and she drops to 74 – head to her room – wake her up to eat some sugar. I watch and wait – she drops into the 60’s – head back to her room – wake her again and make her eat some more..

and that, my friends is how we ended up at a lovely blood sugar reading of 52 this morning.

Fed up with a blood sugar that would not come down, frustrated with an inaccurate reading from Dex that we rely heavily on and mad at myself that I didn’t just change her site before bed and just wanting to SLEEP.

I, her mother, gave her a dose of insulin that caused a dangerous low blood sugar..

To be fair – we will never actually know whether it was the exercise finally catching up with Eden or the dose of insulin I gave her that caused it. Her Dex could have been accurate the entire time and she could have had residue on her fingers causing an inaccurate finger prick. It could have been a combination of all of those things and/or her site could have been functioning just fine and we were only dealing with a stubborn high??

no way to know whether it was my fault or not… But I am her mother and I am in charge of keeping her ALIVE during the overnight hours.. the guilty feelings will ALWAYS creep in – even though we do the very best we can with what we have…

 

So – not only did I save my child’s life today – I could easily have taken it away..

It could have been MUCH worse and those thoughts will plague me today… a hard thing to swallow for sure but I cannot dwell on it too long.. 

It is our life – walking that tightrope every.single.day. and some days we fall off..

But we bounce back and do it all over again because we have no other choice.

THAT is the Type 1 Diabetes life.. 

 

WE NEED A CURE…

My human guinea pig …

We had our Endo (specialist doctor) appointment on Tuesday – a day that we really do not look forward to.

I went into the appointment with a list of questions, comments and concerns – MANY more than usual – and the fear that I would let my frayed emotions get the better of me.

We have had SO MANY issues with T1D lately and it has been ridiculously, frustratingly, HARD. I hate the feeling of trying to explain how/why Eden’s blood sugars have been so high and whacked out. Thankfully her Dr. is amazing, kind and incredibly supportive and encouraging.

 

The thing is, I’m kind of off the hook.

I can only do so much with her D care and management and SHE needs to do the rest. 

BUT, I’m kind of also ON the hook too because I’m her parent and it’s my job to ensure she is safe and healthy. 

 

Eden is not at the point of being able to completely self-manage. Among other things, I keep track of site change days, insulin levels in her pump, CGM sensor changes and inserting the devices into her body. Eden does not make any changes to the insulin dosages that are programmed into her pump either.

I do that. 

The only way to do that is to track trends and consistently ask questions of Eden to determine whether changes might even need to be made. Increasing the amount of insulin Eden gets is not a thing to mess around with – I take it very seriously and do my darndest to fine tune things to the best of my ability.

Eden gets a steady stream of insulin (called basal insulin) 24hours a day – as well as needing insulin for meals or high blood sugar (those rates vary too). Her basal insulin requirements vary dramatically depending upon the time of day. Currently she has NINE basal rate settings programmed into her pump that I tweak up/down and change the time around. An hour here or there makes a difference – and getting those settings just right is a near impossible feat lately.

 

The only true way to test whether Eden is getting the correct amount of basal insulin is to do basal rate testing – which requires her NOT to eat or exercise – so we can see if her blood sugar rates remain steady over whatever period of time we are analyzing. For the past 4 days we have not allowed Eden to have a snack in the morning at school so I can get a better idea of what is happening with her blood sugars. Thank goodness I can monitor from afar with the use of Dex and Nightscout – or she would be needing to test her blood sugar every 30-60 minutes.

The gradual changes I made over the last few weeks have not been working. The doctor helped with some suggestions which I applied but they still weren’t making ANY difference. This morning, being completely fed up, I decided to go super aggressive on the changes and told Eden ONE more day of no snack..

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Well – that didn’t work..

Eden’s blood sugar went low at the tail end of PE today (hopefully not from my changes) so she needed to treat herself with some fast acting sugar. PE is another story all together – never the same level of exercise 2 days in a row – so very hard to manage.

 

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I watched from a distance as her blood sugar slowly crept from low, to in-range and then higher and higher and higher, into crazy high ONCE AGAIN.

 

I now have no idea whether she over treated the low and that contributed to the rising blood sugar levels or my aggressive basal rate changes were NO WHERE near aggressive enough??

The reality – my poor kid is really nothing short of my human guinea pig.

Every day we are taking our best guess with the information we have and giving her medication that can kill her based on those guesses…

no snack again tomorrow for my girl as we try to figure out the mystery and exactly WHICH basal rate I need to change by a little or a lot.. pretty sure we need an overhaul for other settings too – but basal rates is the place to start.

Type 1 Diabetes seriously has a mind of it’s own – it makes absolutely NO SENSE some days and changes the rules whenever the heck it wants to. There is ALWAYS something to keep us on our toes – D never rests and lately seems to be getting the last laugh.

 

WE NEED A CURE

that is all …

things with Type 1 Diabetes have NOT been easy around here lately..

 

 

ridiculous high blood sugars, ketones, not testing, not bolusing.

normal pre-teen eye rolling – I’ve got this – I don’t need you attitude

bad moods, frayed nerves and feeling like bashing my head against a brick wall.

 

all around hard – because T1D NEVER goes away.

We NEVER get a break from it

 

 

Eden is tired of dealing with it.

I am tired of dealing with it.

Our entire family is tired of dealing with it.

 

But we have NO CHOICE.. 

we have to take the good with the bad – celebrate the little victories that lately seem few and far between.

 

Most days we remain positive and upbeat.

Today is not one of those days..

 

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Today, I HATE Type 1 Diabetes.

My heart breaks for my daughter because it really just isn’t fair. 

I HATE seeing her upset by this disease and having to go through what she does.

Today, I want it GONE. 

 

 

 

that is all…

 

 

what comfort zone?

A little known fact about me – I hate politics…

ANYTHING to do with politics, government going on around me and I tune out. 

completely.

Should I care – probably..  but it goes back to my high school days (a LONG time ago) ..

short version of events and how I remember it going down. In high school I wanted to either be a doctor or a lawyer. There were prerequisite classes that needed to be done to set me up for entry into university. My school counsellor was of the opinion that I should go into politics and put me into that class and not what I actually wanted to do. I HATED it. I REALLY wanted out – but was not given that option.. It turned me against school and eventually lead me to dropping out of high school.

Yup – I have a rebellious streak and it has lead me into a lifelong dislike for ANYTHING related to politics or government.

SO – when I was asked by our local JDRF Chapter to write a letter to our local Congressman so that the JDRF Government Chair could take it to Washington DC in March – I have to admit I was totally put out of my comfort zone. My first gut reaction was UGH. I just saw the word Government and I went UGH.

Silly – I know… but it was my natural first gut instinct.

Of course, I sucked it up and wrote the letter…

I would do pretty much anything to help find a cure to Type 1 Diabetes for Eden – although I don’t think you will see me personally in Washington DC anytime soon..

 

below is my letter.. will it make a difference – I really don’t know..?

but I am certainly willing to give it a try.

I love her THAT much .. 💖

 

Dear Congressman …..,

Currently, my biggest hope, dream and wish for the future is a cure for Type 1 Diabetes (T1D). 

Why? 

Because our life changed forever almost 5 years ago when my daughter Eden (7) was diagnosed with this incurable, sometimes life threatening, misunderstood, auto immune disease.

Why contact you?

Because you have more power than I do to create change and help fight for funding for research to find that cure – and I need your help. Eden needs your help.

Our story is becoming one that I hear all too often. Another child being diagnosed with T1D and being thrown into the world of fear, heartache and anguish as we are forced to act as one of our child’s internal organs to keep them alive 24hrs a day 7 days a week 365 days a year. One wrong calculation can mean the death of your child – now that is immense pressure!

Type 1 Diabetes is an auto immune disease that causes our children to be insulin dependent for LIFE. Living with T1D is a very difficult balancing act as we juggle the physical and emotional burdens that it imposes. There currently is NO CURE and although insulin treatment allows Eden to live – it is only possible by her being subjected to 8-12 finger pricks a day to test her blood sugar, accounting for every single item of food that she eats and trying to maintain blood sugar levels when everything she does makes a difference. A blood sugar too low is immediately dangerous and too high puts her at risk for long term complications creating a very difficult balancing act.

Eden wears an insulin pump that infuses insulin into her body 24 hours a day and a CGM (continuous glucose monitor) to help manage her T1D – but these require insertion via big needles every 3 and 7 days respectively. They are only tools – medical devices – which help sustain her life. Without insulin – Eden will DIE. What we really need and want is a biological CURE so that Eden and all the other people living with Type 1 Diabetes can live a life without needles, being attached to medical devices or having to consider T1D in every single decision they make in their day. 

Eden is now at the age (almost 13) where she is needing and wanting to try to manage her disease on her own. It is also a very delicate age where she is trying to find herself, fit in with her peers and doesn’t want to be different. That alone is hard as a pre-teen, let alone factoring in wearing 2 medical devices attached to your body and having to make medical decisions that keep you alive all day long. Decisions that she will never get a break from – EVER.

As her mother, it is incredibly exhausting, frustrating and sometimes scary as I try to teach her about managing a complicated disease where one wrong move can cause death, but also giving her the freedom to live her life without fear and hovering. As Eden grows older the burdens will entirely be on her shoulders – right now I try to ease the burden as much as possible. I wake multiple times during the night to test her blood sugar, I keep an extensive medical plan in place at her school to ensure she is safe, I advocate for her wellbeing and education with teachers and coaches, the costs drain our bank account, I spend hours on the phone with insurance companies, keep track of blood draws, doctors appointments, her prescriptions and of insertion days (for medical devices) and I also inflict the pain on my daughter to keep her alive. 

The general population does not understand what living a life with Type 1 Diabetes is truly like. It is a daily roller coaster ride of emotions that we cannot escape. Eden does not let T1D hold her back and we will not allow it to determine what she can and cannot do with her life. We attack this disease as a family and do what needs to be done to allow her to live as good a life as possible. Eden is an amazing daughter, friend, sister, student, athlete and T1D advocate and my biggest hero.

The T1D life is not easy – but for the most part we make it look easy – because right now, we have no other choice than to live with it.

I hope you will join me in my mission, my dream, to help educate the world and find Eden a cure for Type 1 Diabetes. Help me to educate and fight for the funding that is so desperately needed. Not only will a cure make a difference in our lives – but in the lives of future generations that may be diagnosed today, tomorrow or next year. 

Thank you in advance for your support.

Sincerely Yours,

I guess we will see …

So all of you who read regularly know that basketball is a huge part of our lives.

Eden lives and breathes basketball 🏀❤️

 

Over the years she has had many different coaches – this always makes it difficult for me as to whether or not to even bring up the big “D” word. Some of them have been basically kids themselves – and I didn’t feel the need to put that on their shoulders – especially since I am always there.

 

They would see her test her blood sugar – some would question Eden – some wouldn’t.

I just learned fairly recently that Eden told one of them a few years ago that she had diabetes – but not the “fat kind”. 

out of the mouths of babes – hey – at least she told him 😳

 

anyway – the coach of her current team has known Eden for many years. He has worked on and off with her but not necessarily on a consistent basis. He knows she has Type 1 Diabetes – he recently joined and supported us when we were doing the JDRF Walk to Cure Diabetes in October. He actually missed a tournament game to support our family.. 💙

 

Last night was the first time he actually noticed that Eden has not “right”. She had missed practice on Monday night – something we NEVER do. If there is practice – we are pretty much ALWAYS there, and then some.. Missing practice was D related and he knew that so maybe it was on his radar? He was actually concerned enough to ask Eden if she was OK and to call out to me during practice to make sure she was alright.

 

She was – but she wasn’t.

Her blood sugar was high – very high.

 

  • she was moving in slow motion
  • she had a dazed look on her face
  • she was not reacting to the ball or following instructions well
  • she totally airballed a 3 pointer

 

After practice he called me – he reached out and I was so thankful.

He wanted to know and understand more so he could help.

To know that there will be another set of eyes watching out – helping Eden to put her health first is going to be a wonderful thing.

 

There is SO much to know and learn – what to say when you have to start at the beginning? 

 

this was my attempt

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Type 1 Diabetes doesn’t and shouldn’t limit Eden – but it DOES very clearly affect her ability to perform at the best of her ability when her blood sugars are out of whack. Unfortunately that is more often than not lately. Even more unfortunately is the fact that Eden THINKS she is totally fine when she clearly is NOT.

 

I’m hoping the fact coach noticed – means that she will WANT to take more care and responsibility.

Diabetes or not – poor performace will see more bench time and less court time. 💔🏀

you would think that would be a pretty big motivator..

 

I guess we will see