_littlewing Dallas bound & down, baby. I wish you the world, B! 4d

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_littlewing W O R L D S E R I E S 6d

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_littlewing "why are your sunglasses on at night?" "because I don't know how long I'm gonna be fuckin' partyin', & I don't know where I'll wake up" 3w

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_littlewing I cannot breathe. 4w

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Amaro Spencer Jewell Dean

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_littlewing Plaza Art (dog) Fair. #Cash 1mon

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_littlewing me too, Biggie Smalls. 1mon

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_littlewing I'm coming for ya #AndYouSayChiCity 1mon

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_littlewing just BEAN cool 1mon

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_littlewing special shoutout to these mamas for helping to make my 25th so great. love y'all 1mon

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_littlewing Iceberg! Right ahead! 2mon

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_littlewing would you just look at this beautiful bride..... #KratzerWedding 2mon

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_littlewing Congratulations, Mrs. Kratzer! love, love, love you @bavanshee #KratzerWedding 2mon

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_littlewing Annual Martinis, Women & Shoes - Heartland Women Leadership Council fashion show. love being a part of this! 2mon

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_littlewing No coast... Random... Oceanless... #KansasCity 2mon

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_littlewing my job sucks. 2mon

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_littlewing Reposting this from a few months back. I'd like to give my thanks, & show my appreciation to those pouring ice water over your heads to raise awareness for ALS For those of you who don't fully understand the disease, read the novel below. The #ALSIceBucketChallenge has helped to surpass the $10 million dollar mark in donations.Thanks, y'all ️ Freezing your asses off is truly making a difference! --- ALS is one of the most heartbreaking diseases I have ever seen strike a human body due to it's rapid, & persistent attack on the nerves responsible for controlling voluntary muscles, all while the brain remains fully functioning, & completely coherent as to what is happening to the body. I cannot imagine losing my ability to move, or speak, & my only form of communication being a blink of an eye - yet still knowing exactly what's going on around you, & knowing, & feeling your decrease in abilities each & every day. •

My dad is the epitome of a "businessman", & is straight to the point in every aspect of his life, yet still finds a way to have the softest, most sensitive heart among many I know. I've seen my dad cry on 2 occasions - once at my grandpa's funeral, & the second every year we attend the ALS Night of Hope charity event. •

Last night the ALS Association not only broke their record of 60k raised in an evening, but broke the record of the largest 1 sum amount donated by a single person. I am proud to say my father is the one to break that record last night, & donate to the ALS Association not just simply money, but hope in finding a cure. •

My uncle was a college professor who showed no signs of such disease until my dad took notice of his brothers speech becoming more & more slow. In highschool, he acted as my tutor in math, which is just IMPOSSIBLE for me to wrap my mind around, but he always remained patient. Today he cannot write, nevertheless pick up a piece of chalk. •

Both men are beyond courageous, & the definition of fighters. ALS is incurable, & fatal with median survival of 3 years. Last night marked the 3rd year of us attending this event. Keep strong, Uncle Paul. We love you dearly!
2mon
  •   mcdoc32 That's an amazing story!! 2mon

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_littlewing my loves forever 2mon

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