IT'S NOVEMBER!!!!!!!! That means it is Nation Diabetes Awareness Month!! What better way to celebrate this month than to raise a little cash for a fabulous cause???? We did that yesterday!!
Yesterday was amazing. Seriously, out of this world, larger than life, amazing!
We have all been trying to raise money to help my best friend, Jennifer, get her daughter a Diabetic Alert Dog, also know as a D.A.D. The family is working with a company called Warren Retrievers. These life saving animals are very expensive. The company puts you on a waiting list after you raise a $1,000.00 deposit. This town amazingly helped the family raise the deposit in a matter of days and they are now on the list. The dogs are however between 15 and 20 thousand dollars. They have 2 years to raise the money and yesterday was the first large fundraiser held. It was a 5K. One of our friends, Candi, put it all together, with the help of the Abilene Runners Club (This is their site if you want to check them out) and did an amazing job! There were just over 100 runners yesterday. I believe it was a total of 113, to be exact. That number included The Abilene Derby Dames, who put a team together and roller skated the whole 5k!! There was also the sweetest group of kids that saved their change and donated it. As well as a woman running alone who donated $50 which was more than the price of a group rate. So many people showed up ready and willing to write a check. So many people were curious to know and learn about Type 1 diabetes. The people that showed up were people who actually cared, people who wanted to make this happen, people that wanted to be a part of something special. That is my exact idea of what the of definition of "community" should be.
HOLY CRAP!!
I am still reeling over how awesome it all was! It was amazing to take in. It was also so very emotional!
I feel so blessed to live in such an amazing town. The out pour of support in the Abilene Community is simply incredible! It is just so filled with love and the people here jump at the opportunity to help! You don't have to state your case and then wait to see if they deem you worthy of their help. The community just jumps in and volunteers. No questions asked! There is still a lot of money to be raised but yesterday put them one step closer to getting there. Thank you to all that participated! This family holds such a special place in my heart. They are my second family and I will do anything, including posting this blog a million times over to get donations! hehehehehehe You can check out some 5k pictures by scrolling to the bottom.
Do you want to know what series of events lead to all of this? You can read the blog I wrote by clicking HERE.
Want to learn more about the cause? Click HERE for the news story.
Would you like to donate by getting something in return?? Buy one of the beautiful Ashley Rings!! They are $15 and every penny of the $15 goes directly to Ashley's fund thanks to the amazing Tommy and Christine Moore!! Check out this local husband and wife team of Jewelers!! They have a Facebook page!! Follow this Link to Oak Tree Jewelers facebook page or click HERE!!! to purchase directly from their Etsy shop. This could very well be your one stop Christmas shop this season :) You can also read about how awesome they are in the Abilene Reporter News by clicking THIS link!
Oh and don't forget to check out Ashley's Facebook page Meet the Ashley Team!! <---click it and like it :)
Most importantly, are you willing to donate?? You can CLICK ME!! CLICK ME!! CLICK ME!!!!! go to the bottom of the page and click donate. It will take you to a paypal account. They will contact you to see who you want the money to go to by which you can respond happily and proudly "THE BOLDEN FAMILY!!"
Do you want to learn more about Type 1 Diabetes??
Go visit JDRF's website! More and more children are being diagnosed this year and ALL parents should know the signs!!!
Showing posts with label diabetes. Show all posts
Showing posts with label diabetes. Show all posts
Sunday, November 13, 2011
Friday, September 16, 2011
The Never Ending Story, needs a Happy Ending Already!! Please?
My heart is aching today. Not for me but for a total stranger. Actually for a whole community of total strangers. It is also hurting for a friend. My best friend. Today, a family in Abilene suffered a loss. A horrible, disgusting, unnecessary, tragic loss. The worst part is that it was a child they lost.
A Child!!!!!!!
I cried. It sickens me. It sickens me even more that it was a child lost to Type 1 Diabetes. There should be a cure by now!! This isn't your everyday, run of the mill kind of diabetes. This is not a disease you get from poor dieting and lack of exercise. It's not something you do to yourself! This is an autoimmune disorder that can happen to ANYONE!! So, where is the cure? Where??? Why are so many children losing their lives to this disease and having to live this way....in fear? How can there be so many advancements in technology to help those suffering from this sneaky, life altering disease but no answer as to how to fix it?
Politics? Money? Greed?
Yes, I am certain all three are playing a roll in this and it's not fair!! The parents and the children deserve an answer!! They have lived in fear long enough. I watch all of these stimulus bills fly through congress full of earmarks. I watch the millions, no, wait, billions of dollars in earmarks going towards parking garages, swine waste management, small fruit research, The Paper Industry International Hall of fame and so on and so forth. These selfish, ignorant jerks do it just to have their name on something. Why would you want your name on things so ridiculous?? Why not put the money to good use?? You know, like researching diseases and helping to prevent them and cure them. If I were a senator and I had my name go on something it would not be on "the Paper Industry International Hall of Fame"!! I would want it to go on a State of the Art building that was cranking out cures that save lives!! Doesn't that make sense?? Yes, yes it does...to people like me and you. Those of us who have souls that haven't yet been sold for campaign contributions and political gain.
Lord knows these politicians DO NOT want to piss off these pharmaceutical companies who donate millions in campaign contributions with the return favor of only finding life long drug fixes for diseases rather than life changing cures!! As long as the money is rolling in what do they care??
I am so disgusted having to see families suffer through this kind of heartbreak! I am tired of watching young kids constantly having to shed blood for the disease. I'm tired of the blue candles burning and I'm tired of seeing the word "HOPE" on everyone's hands when I know inside that they just feel hopeLESS at times.
I can't imagine the pain of having to live with a constant fear. I don't ever want to live through it with my own children but I am an outsider who watches through the eyes of a family that is very near and dear to my heart and I hate that they are living this hell! I am also not blind to the fact that this could happen to my kids or anyone of our kids for that matter.
It makes it even more real that I have a sister with the disease. A sister who better be taking care of herself!!!
There is nothing that makes you special and will keep your kid from being attacked. So before you ignore this and think "this could never happen to my family" take some time to pray for these people. Yes they are people, they are real, they exist. They are scared mothers and fathers who take turns sleeping because they are scared that they will lose their child, they are children who pray for a cure so that they can quit trying to find a good finger to use to test...a finger that isn't yet calloused from so many pricks. They are beautiful teenager girls who want to wear that beautiful dress to prom WITHOUT having to find a place to put her insulin pump so it won't bulge through that "perfect dress". They are young boys who want to play football without having to stop for a sugar pill, or quick stick because all of that running made them go low, or have to get a shot of insulin because all of that adrenaline made them go high. They are 8 year olds who miss field trips because there isn't enough staff trained to care for them and mom and dad have to work to make sure they have insurance for this overly priced disease. They are 18 month old's with keytone strips in their diapers. And you never know if you will have to join their community someday it may be you on their side asking for prayers.
I wish that everyone would take a moment and light a blue candle to show your support for this family that you may or may not know and for all of the other families with breaking hearts. Also take some time to email your Senators and Congressmen and demand answers and cures not temporary fixes that cost tons of dollars!!! They need to quit being bought by the damn drug companies and start remembering who they are working for!!!! I am emailing them what I wrote in this blog right now. Take some time and email them your feelings too.
My prayers are with all of the families out there dealing with this!!


| This can happen to ANYONE so learn the Warning signs of T1D (these may occur suddenly): | |
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These Pleasant Nightmares are coming from
Tuscola, TX 79562, USA
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