Thursday, April 5, 2018

Teenaged Diabetes Ramblings for Newbies

The girls are continuing to do well with school, activities, work and T1D.  Nothing seems to slow them down.  In general, life is very good and they are living their lives just like any of their peers. They often stay up too late, rather hang out with friends than do homework and love to shop for new clothes.  They also work hard, get good grades and help us around the house.  It's not always perfect but we have a lot of love for these two young people and feel grateful for each moment. 

I think that is something that I always wondered about... what would the teen years be like? 

And most importantly, would our daughters be happy?

The answer... YES!  Yes, they are happy, joyful and sometimes, a bit too spunky!  They are just the way that you would imagine in any other family.  T1D is not overshadowing their joy in the slightest.

I say this to continue to reassure the new families that dealing with a first-time diagnosis.  It may be very overwhelming with learning, coping and managing T1D.  I guarantee though, that in just a few short weeks, life will resume a new normal.  In a few months, you will begin to adjust almost seamlessly and in a few years, you might even forget what it was like before T1D entered the picture.

It gets better, it really does. 

Keep finding your joy!

Hugs,
Naturally Sweet Sisters

PS... Proud mama alert... find the NSS oldest in this article (quote).  She is wise beyond her 16 years! 

http://diabetesstopshere.org/2018/04/05/thisisdiabetes-on-capitol-hill-2018-call-to-congress-recap/









#ADA #C2C018 #ThisisDiabetes

Tuesday, March 27, 2018

ADA Call to Congress 2018



A few days ago, our oldest daughter and I had the pleasure of attending the American Diabetes Association 'Call to Congress', held in Washington, D.C..  And wow!  What a wonderful opportunity it was to speak, share and to listen to over 200 other advocates as they told their own personal stories of living with diabetes.

There are these amazing moments in our lives in which suddenly you realize that you have an ability to communicate not just for yourselves but for the greater world at large.  This was one of those moments. 

As we walked into a meeting with Congressman Mike Bishop, 8th District, of the state of Michigan, I could sense an exciting chance to help further teach what we as patients and families live with through having been diagnosed with T1d.  While we have learned much on our journey and do our best to maintain health, there is nothing more that we would like to have than a CURE.  With this in mind, our meeting started and in a few moments, I watched as my daughter calmly begin to speak. 

This is what she shared:

"Diabetes is a disease that goes with me wherever I go. It is something that I can't ignore or take a day off from.  By looking at me, you might not realize that I am a person living with diabetes.  You would also not know that my little sister and many of my friends have diabetes.  It is truly an invisible disease.  It also does not discriminate and anyone, at anytime, can be diagnosed.  I have watched my friend become diagnosed and I have had to be the support system for them.  This is something that no one has asked for and something that no one deserves.  This chronic and life-threatening disease needs a cure.  That is exactly why research funding is so very important".




Then, she casually pulled out her blood sugar meter and begin the process of checking her glucose.  Congressman Bishop spotted the attached car key and questioned why the two were paired together.  Our daughter explained that when she drives, she must check her blood sugar.  This was a surprise as it was not widely understood that checking happens beyond mealtimes, but also, during sports, activities, parties, holidays, at night and well, even at a Congressman's office. 

The story she shared wasn't overly dramatic but it was honest and authentic.  Checking glucose happens every day, multiple times throughout a day.  It has become such a routine event that we rarely think about the process but in this setting, watching a pretty, well-spoken, young person calmly use a needle lancing device on their finger, only then to squeeze out a blood droplet, felt barbaric.  Even when she correlated the data to her technologically advance Continuous Glucose Monitor (CGM), it still felt like not enough in terms of progress had been made.  There should be more (and better) diabetes treatments.  Where are the implantable sensors?  The true artificial, fully automated pancreas? Research is only as good as the funding it is provided. 

Within the room, there was an empathetic silence in understanding that life with diabetes is difficult.  As she finished speaking, smiling through her testimonial, the reality became even clearer; people living with diabetes need better. Each head around the table nodded in support of improving care and helping our patients and families.  Yes, we can do this! We can make change.

When the meeting ended, we shared our thank you's and exchanged our good-bye's for the time being.  There is more work yet to be done and we will carry on with hope that we are continued to be heard.  You can join our advocacy efforts by attending your own home-town meetings and through sharing your story.  I would love to hear back on your involvement.


Thursday, March 8, 2018

GET INVOLVED - TWO RESEARCH STUDIES

Hi Patients, Families and Friends - 

Just a quick note to share that there are TWO exciting research opportunities through Nemours.  You do NOT need to be a patient or live in the area because these are both fun ONLINE opportunities.  Read more below for qualifying details and please, feel free to SHARE this post to help us fill up their research study so we can improve T1D care for all!!!

Research is the magic medicine of helping to improve care while also feeling EMPOWERED by sharing and bettering our T1D community.  I attest much of the positivism within our family to rolling up our sleeves and giving back in ways that create tangible change and better outcomes for everyone living with T1D.  

If there is just one thing you do, try participating in research - you won't regret it and the payback will be worth every second.  

Best wishes and thank you!

Naturally Sweet Sisters






Research Study #1  Click HERE for details or type in your browser http://bit.ly/TCT1D.





Research Study #2 Click HERE to learn more or type in your browser http://bit.ly/youngT1D

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