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^- I had spent about four weeks, I think it was maybe

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^four to six weeks at combat skills training

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^at Fort Hood, before I left for Afghanistan.

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^It was an immediate departure,

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you just kind of went from one to the next.

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Unfortunately, about two weeks after I arrived

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I was just noticing that I was struggling to kind of wake up

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and I said, "Let me go to the gym."

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And so I would go to the gym and I would try to run,

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I think, one mile, and mind you,

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several weeks before I had gone,

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I was running three or four miles, a day.

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I tried to run one mile and I was struggling.

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I remember I had to take a flight to Kandahar,

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and I ran into my friend that evening,

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and she said, "Kimberly, you look awfully pale.

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"Maybe we should take you to Sick Call tomorrow."

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And I said "Okay," and she did, she took me to Sick Call,

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at Kandahar, and I remember I met a Major

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who took one look at me and she said,

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"I think we need to get you to Kandahar Hospital

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"for a blood draw", and I arrived at Kandahar Hospital

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and I remember they assigned an EMT,

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and they took a lab draw, and a doctor

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came running through and she said,

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"I can't even believe you're alive right now.

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You have no detectable platelets and a hemoglobin of three."

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To have no detectable platelets is extremely serious.

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Anything below ten thousand, you're at risk for stroke,

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brain hemorrhage, to have hemoglobin of three is like

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having one good pint of blood running through your body.

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The night that they were going to take me to Landstuhl,

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they brought a C5, and I remember they took me

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in an ambulance exit night, and I looked outside

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the ambulance window, and there's a C5 on the Tarmac,

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and the back is open and it's a huge aircraft.

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And inside the aircraft, the only thing in it

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is one gurney, one gurney and a ton of nurses,

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or people in gowns and they are all moving about,

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and I'm sitting in this ambulance and I'm thinking,

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"Surely that's not just for me," and it was.

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And it launched til I was met by a Colonel and a Major,

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and they said, "You're not going to Landstuhl,

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"You're going to Walter Reed."

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I think at that point, and they said it was in D.C.,

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I realized just how serious things were.

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(light music)

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At that point, that was the treatment for the

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Aplastic Anemia, and the N.I.H. continues to follow you

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for multiple years after that treatment,

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and they just expected after follow up, that my

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blood counts would resolve over time.

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My red cells were not producing on their own,

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and so I was continuing to receive blood transfusions

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about every three weeks, but during that time

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I was back at work, I was continuing to work on my

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Masters Program, driving across town to go to school,

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and then every three weeks, I would go in and get blood,

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and then go back on my way, and keep working.

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Then spring time, year of 2010,

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my bone marrow started to work,

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and I stopped needing transfusions.

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So it was in remission from the Severe Aplastic Anemia,

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and the treatment worked, and by the fall of that year,

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I went to Professional Military Education

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and Squadron Officers School.

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I was running, again, when they told me that

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I wouldn't be able to do that, and in 2011,

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my Severe Aplastic Anemia evolved into what's called

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Myelodysplastic Syndrome or M.D.S.,

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and that is a precursory chemic bone marrow failure disease.

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The course of action for that was to

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sort of continue to live, so from 2011 onward,

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I was selected to cross train to intel,

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I went to Intel School, I worked shift work,

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I deployed, I took PT tests.

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I did everything, all the while with this,

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while managing my Myelodysplastic Syndrome.

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Then in 2016, I PCS'd to Kirtland Air Force Base.

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I was starting to experience just some different things

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with my skin, and with my eyes.

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I was trying to keep it all together, and keep going to work

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but that became increasingly difficult when

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my platelet count started to drop.

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I had hoped that it was the medication that I was taking

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that was causing my counts to act up,

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and I had a bone marrow biopsy done, and unfortunately

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the biopsy came back to confirm that my

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Myelodysplastic Syndrome had evolved into Leukemia.

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At the moment of diagnosis, the option of

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being part of the Patient Squadron in San Antonio

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or remaining as a member of my unit

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was something that I discussed with my Commander

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and I worked very hard, and she worked very hard,

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to ensure that I remain a member of her unit.

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That I did not PCS because the intention and goal

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was always to get better, and come back to work.

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(light music)

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- I sit here before you, having gone through

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something traumatic, I had to take a knee

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for a while, but it was temporary.

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This challenge wasn't about to stop me.

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It was brought to bring me closer to my destiny,

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and sometimes you find yourselves in

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overwhelming, unexpected situations,

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and when we do, we lean on our faith,

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on our family, and on our friends, and I lean on my faith,

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and on my incredible family, and my friends still.

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Not every day is an easy one,

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but it's about believing for good things,

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and continuing to move forward, and choosing to live.

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And, I choose to live.

