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	<title>Diagnosis Archives - Fanconi Cancer Foundation</title>
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		<title>From Shock to Strength: Our FA Diagnosis</title>
		<link>https://fanconi.org/from-shock-to-strength-our-fa-diagnosis/</link>
		
		<dc:creator><![CDATA[Sherri Van Ravenhorst]]></dc:creator>
		<pubDate>Mon, 22 Jul 2024 19:37:11 +0000</pubDate>
				<category><![CDATA[Stories]]></category>
		<category><![CDATA[Diagnosis]]></category>
		<guid isPermaLink="false">https://fanconi.org/?p=4416</guid>

					<description><![CDATA[<p>It took me weeks to come to terms with the fact that there were no easy answers. I couldn't change the past or the diagnosis, so I focused on educating myself and becoming Tinslee's biggest advocate. We underwent all the necessary tests, scans, and procedures, and spent a year going in for lab work and check-ups.</p>
<p>The post <a href="https://fanconi.org/from-shock-to-strength-our-fa-diagnosis/">From Shock to Strength: Our FA Diagnosis</a> appeared first on <a href="https://fanconi.org">Fanconi Cancer Foundation</a>.</p>
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<p>By Alex Taylor</p>



<figure class="wp-block-image size-large"><img fetchpriority="high" decoding="async" width="1024" height="683" src="https://fanconi.org/wp-content/uploads/2024/07/Tinslee-1024x683.jpeg" alt="" class="wp-image-4417" srcset="https://fanconi.org/wp-content/uploads/2024/07/Tinslee-1024x683.jpeg 1024w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee-300x200.jpeg 300w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee-768x512.jpeg 768w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee-1536x1024.jpeg 1536w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee-2048x1365.jpeg 2048w" sizes="(max-width: 1024px) 100vw, 1024px" /></figure>



<p>Hi! My name is Alex, and I am a single mom to my almost 4-year-old daughter, Tinslee. We discovered Tinslee has Fanconi anemia (FA) the same day we first learned about the condition. At her two-year check-up, her pediatrician recommended blood work because Tinslee hadn&#8217;t been growing as expected. This led to a referral to the Hematology Oncology department at Children&#8217;s Mercy Kansas City. After months of testing, we received the diagnosis.</p>



<p>Initially, we had no warning signs apart from her being very petite. The diagnosis brought an overwhelming mix of shock, disbelief, and heartbreak. I made the mistake of Googling FA, and what I found shattered me. I spent the first two days in tears, questioning why this was happening to my daughter. I wondered why children get sick and turned to prayer, hoping to find solace in a bigger picture. Although I had never been very religious, I needed something to hold onto.</p>



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<figure class="wp-block-image size-large"><img decoding="async" width="683" height="1024" data-id="4423" src="https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-683x1024.jpeg" alt="" class="wp-image-4423" srcset="https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-683x1024.jpeg 683w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-200x300.jpeg 200w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-768x1152.jpeg 768w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-1024x1536.jpeg 1024w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-1365x2048.jpeg 1365w, https://fanconi.org/wp-content/uploads/2024/07/Tinslee3-1-scaled.jpeg 1707w" sizes="(max-width: 683px) 100vw, 683px" /></figure>



<figure class="wp-block-image size-large"><img decoding="async" data-id="4422" src="https://fanconi.org/wp-content/uploads/2024/07/Tinslee4-1-768x1024.jpeg" alt="" class="wp-image-4422"/></figure>
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<p>It took me weeks to come to terms with the fact that there were no easy answers. I couldn&#8217;t change the past or the diagnosis, so I focused on educating myself and becoming Tinslee&#8217;s biggest advocate. We underwent all the necessary tests, scans, and procedures, and spent a year going in for lab work and check-ups.</p>



<p>One day, I was added to the Fanconi Cancer Foundation (FCF) support group on Facebook. Finally, I had a community of people who understood our journey. They encouraged me to seek a second opinion. Although we had been receiving care at Children&#8217;s Mercy Kansas City, they didn&#8217;t have an FA specialist. The closest specialist was in Cincinnati, so we drove 10 hours straight for Tinslee&#8217;s appointment. We left feeling encouraged and empowered.</p>



<p>Tinslee is now preparing for a bone marrow transplant in Cincinnati. We don&#8217;t know when it will happen, but we are confident she will receive the best care possible. While I still have moments of random tears or anger at the world for the hand my daughter was dealt, I find strength in the support of our family, friends, and community. Together, we will make it through.</p>
<p>The post <a href="https://fanconi.org/from-shock-to-strength-our-fa-diagnosis/">From Shock to Strength: Our FA Diagnosis</a> appeared first on <a href="https://fanconi.org">Fanconi Cancer Foundation</a>.</p>
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