Dawson’s Journey: Fighting a Rare Childhood Cancer

Dawson, 8, faces rare LCH; funds will cover scans, port placement, and chemo

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Dawson’s Journey: Fighting a Rare Childhood Cancer

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On January 19th, the Griep family received devastating news: Dawson (8) has been diagnosed with Langerhans Cell Histiocytosis (LCH). LCH is an extremely rare form of cancer that most commonly affects children ages 1–3, making Dawson’s diagnosis at his age even more uncommon. Essentially, his body is attacking itself and creating tumors.

At this time, Dawson has two known masses. One is located on his mastoid bone and has completely deteriorated the bone, causing the mass to press against his brain. Thankfully, his brain is not currently affected. The second mass is on his femur. Both cause him pain, yet Dawson has been an absolute trooper through it all.

Next week, Dawson will undergo a full-body scan to determine if there are any other areas affected. We are praying this does not reveal anything further. Following the scan, he will have a port placed and will begin chemotherapy.

While this diagnosis is overwhelming, LCH is a cancer that can be fought, and treatment outcomes are very promising. We are incredibly grateful for the amazing oncology team and specialists caring for Dawson, and thankful that we now have answers and a plan in place. We are ready to fight alongside him.

There are still many unknowns ahead, and this journey is only beginning. Dawson’s care will continue at Children’s Hospital of Milwaukee.

Any donation to help support the Griep family during this incredibly difficult time would be deeply appreciated. Thank you for your love, prayers, and support.

Co-organizers3

Brittiney Belche
Organizer
Richland Center, WI
Alison Griep
Beneficiary
Mackenzie Kaney
Co-organizer
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