Support Courtney's Fight Against A Rare Cavernoma

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Support Courtney's Fight Against A Rare Cavernoma

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Hello, I am a friend of Courtney's. We met many years ago at Patriot Sports, and even though we haven't seen each other in person in awhile, we get to keep up via Facebook and I love following her and her sweet family!

As many of you know, Courtney has been diagnosed with a very rare cavernoma, also known as a cavernous malformation (an abnormal cluster of blood vessels in the brain or spinal cord that can leak blood, potentially causing seizures or other neurological issues).

Courtney's diagnosis is so rare, she is having trouble finding help with her symptoms and answers on how to get rid of it. There are out-of-state specialists that she is looking into now, but these options are extremely costly and I thought we could lighten their load and help them out with funds to help with her medical bills and second opinions that sometimes run as much as $900.

I know we all love Courtney and her sweet family, so let's rally around them and show her some love. When many of us don't know how we can help and it leaves us feeling helpless, she is blessing us and giving us a way to help support them. God calls us to help those in need, and she is in need at this time, so let's get the word out and bless her family with some assistance and DAILY prayers.

We know the power of prayer works, and we can all send them up along with all the good vibes we can send her way. Thanks in advance for blessing the Parker family.

Please share this with all your friends and family who might know the Parker family and want to help.

Organizer and beneficiary

Laura Teran
Organizer
Austin, TX
Courtney Parker
Beneficiary
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