We prayed for a miracle which God granted in heaven. Daily we walk the path of grief, ever leaning on Jesus for our comfort. Until we meet again Millie, always remember you are forever loved and missed!

Wednesday, September 1, 2021

𝙄 𝙬𝙞𝙡𝙡 𝙨𝙝𝙖𝙧𝙚 𝙩𝙝𝙚 𝙝𝙚𝙖𝙧𝙩𝙗𝙧𝙚𝙖𝙠 𝙤𝙛 𝘾𝙝𝙞𝙡𝙙𝙝𝙤𝙤𝙙 𝘾𝙖𝙣𝙘𝙚𝙧


 


𝐒𝐞𝐩𝐭𝐞𝐦𝐛𝐞𝐫 𝐢𝐬 𝐭𝐡𝐞 𝐦𝐨𝐧𝐭𝐡 𝐬𝐞𝐭 𝐚𝐬𝐢𝐝𝐞 𝐭𝐨 𝐫𝐞𝐜𝐨𝐠𝐧𝐢𝐳𝐞 𝐂𝐡𝐢𝐥𝐝𝐡𝐨𝐨𝐝 𝐂𝐚𝐧𝐜𝐞𝐫
𝑩𝒖𝒕 𝑾𝑯𝒀 𝒘𝒐𝒖𝒍𝒅 𝒂𝒏𝒚𝒐𝒏𝒆 𝒘𝒂𝒏𝒕 𝒕𝒐 𝒓𝒆𝒄𝒐𝒈𝒏𝒊𝒛𝒆 𝒔𝒖𝒄𝒉 𝒂 𝒘𝒓𝒆𝒕𝒄𝒉𝒆𝒅 𝒂𝒏𝒅 𝒂𝒘𝒇𝒖𝒍 𝒅𝒊𝒔𝒆𝒂𝒔𝒆?
{{Please SHARE for awareness}}
Because every year in the U.S. there are an around 15,780 children between birth and 19 years old who are diagnosed with cancer. Approximately 1 in 285 children in the U.S. will be diagnosed with cancer before their 20th birthday. Around the world there are more than 300,000 children diagnosed with cancer each year.
Our daughter Millie was one of those statistics in 2019. We were that family that heard the devastating words, “I’m sorry it looks like she has cancer.” Those horrible words that would forever change our family. No longer would we live without the scars of cancer.
Millie fought Neuroblastoma from June 20, 2019, to July 8, 2020. On that day she became one of the approximately 1800 children who would lose their life to cancer that year. Cancer remains the most common cause of death by disease for children in America.
I share this to remind you that research is the key. Finding a treatment for cancer is important to the future of our children, however it is a huge task. The term cancer covers close to 200 different diseases. I have friends that have children who have fought:
• Wilms cancer,
• Acute Myeloid Leukemia
• Acute Lymphoblastic Leukemia
• Hodgkins Lymphoma
• Ewings Sarcoma
• Langerhans Cell Histocytosis
• Juvenile granulosa cell
• Neurofibromatosis 1
• Medulloblastoma
• Retinoblastoma
• Neuroblastoma
• DIPG
With each of these ‘cancers’ the treatment is completely different. What Millie received is nothing like the treatment our friend Leavyn goes through as she battles Leukemia. The testing that Mille had is not the same tests our friend Blaise had when he was diagnosed with Wilms.
With such individual diseases, it takes a lot of funding to research each one. Currently, only 4% of federal cancer research funding is dedicated to childhood cancer. Our children are worth #MoreThan4 percent of the funding. Millie was worth more than 4!
𝗧𝗵𝗲 𝗺𝗼𝗻𝘁𝗵 𝗼𝗳 𝗦𝗲𝗽𝘁𝗲𝗺𝗯𝗲𝗿 𝗜 𝘄𝗶𝗹𝗹 𝗯𝗲 𝘀𝗵𝗮𝗿𝗶𝗻𝗴 𝘄𝗵𝗮𝘁 𝗰𝗵𝗶𝗹𝗱𝗵𝗼𝗼𝗱 𝗰𝗮𝗻𝗰𝗲𝗿 𝗶𝘀 𝘁𝗼 𝗺𝗲, 𝗠𝗶𝗹𝗹𝗶𝗲’𝘀 𝗺𝗮𝗺𝗮.
𝗪𝗵𝗮𝘁 𝗶𝘁 𝘄𝗮𝘀 𝘁𝗼 𝗠𝗶𝗹𝗹𝗶𝗲’𝘀 𝗱𝗮𝗱𝗱𝘆, 𝗵𝗲𝗿 𝘀𝗶𝗯𝗹𝗶𝗻𝗴𝘀, 𝗵𝗲𝗿 𝗻𝗶𝗲𝗰𝗲𝘀, 𝗮𝗻𝗱 𝗻𝗲𝗽𝗵𝗲𝘄𝘀.
𝗜 𝘄𝗶𝗹𝗹 𝘀𝗵𝗮𝗿𝗲 𝘄𝗵𝗮𝘁 𝗰𝗵𝗶𝗹𝗱𝗵𝗼𝗼𝗱 𝗰𝗮𝗻𝗰𝗲𝗿 𝘄𝗮𝘀 𝘁𝗼 𝗮 3-𝘆𝗲𝗮𝗿-𝗼𝗹𝗱 𝗹𝗶𝘁𝘁𝗹𝗲 𝗴𝗶𝗿𝗹.
~~~𝙄 𝙬𝙞𝙡𝙡 𝙨𝙝𝙖𝙧𝙚 𝙩𝙝𝙚 𝙝𝙚𝙖𝙧𝙩𝙗𝙧𝙚𝙖𝙠 𝙤𝙛 𝘾𝙝𝙞𝙡𝙙𝙝𝙤𝙤𝙙 𝘾𝙖𝙣𝙘𝙚𝙧~~~
Blessings sweet friends…
☆。・:*:・゚★,。・:*:・゚☆ 。・:*:・゚★
I still believe in Millie’s Miracle
☆。・:*:・゚ Hebrews 11:1 。・:*:・゚☆
︵‿︵‿୨☆୧‿︵‿︵

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