THE STORY OF ONE FAMILY'S JOURNEY WITH TYPE 1 DIABETES AND CELIAC DISEASE.
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Showing posts with label #dka. Show all posts
Showing posts with label #dka. Show all posts

Friday, February 11, 2011

In The Nick of Time.

Fatigue
Dry mouth.
Frequent urination.
Thirsty.
Itchy spots.
Abdominal pain.
Vomiting.
Headache.
Blurred vision.
Increased respiration rate.
Weakness.
Worsening abdominal pain.
More urination.
More vomiting.
More pain.
Terribly thirsty.
Tired.
Worsening weakness.
More vomiting.
Unable to move.
Faster respiratory rate.
Excruciating abdominal pain.
Can't focus.
Abdominal distention.
Gasping for air.
Worse headache.
Hurts to breath.
Worsening thirst.
Generalized swelling.
More swelling.
Eye swell closed.
Can't see.
Shallow, labored respirations.
Still thirsty.
Urinary incontinence.
Pain.
Can't think.
Pain.
Thirst.
Air.
Weak.
Pain.
Head too heavy to lift.
Awake.
Confused.
Asleep.
Awake.
Asleep.
Coma.
Seizure.
Death.

Diabetic Ketone Acidosis (DKA).  Inevitably this is what will happen if your body doesn't produce insulin and you are unable to access medical intervention in time.  It can happen very slowly or things can go downhill very quickly.  Suffering is always part of process, and the end result is NEVER survival.

When Sugar was diagnosed, she was very close to the end of the list...fortunately, we were able to get a diagnosis, an ambulance, and an insulin infusion in the nick of time.

Sadly, that isn't the case for many families more often than we'd like to believe.  Somewhere today a child will succumb to Type 1 Diabetes because their family cannot access the insulin he or she needs to survive.

Please pray for this child's comfort....the broken hearted family....the turmoil that will be left behind.  Pray for the situation.  Pray that someone, somewhere, somehow can get insulin to these innocent children in time.  Pray that they'll be able to continue accessing it in order to keep their child alive.

Say BIG PRAYERS.  It's a BIG PROBLEM.

And then, please pray for Candy Hearts and the journey that begins unfolding on

2/14/11.
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While I'm happy to share our experiences with what works, and what doesn't work, for the management of Type 1 Diabetes and Celiac Disease in our house, please do not mistake anything you read here for medical advice. Decisions regarding your/your child's health care should be made only with the assistance of your medical care team. Use any information from this blog at your own risk.