Camp Diasozo

05/30/2021

If eyes are the windows of the soul, does that make morphea windows to the vascular system??
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05/24/2021

Nothing let’s off some steam like playing in the mud! 💙

04/18/2021

Having a chronic illness is HARD and so many of us struggle with the day to day aspects of it. You are not alone! How can we pray for you today??

03/24/2021

Happy spring! Who else 😍 flowers?? These are ‘I’m sorry I put together your IKEA furniture without you’ apology flowers but who’s counting!

02/15/2021

Happy Valentine’s Day from a snow covered Texas! 🥶😍

02/03/2021

Congratulations to Michelle!!! Keep up the good work, Michelle, and show the world what a fighter you are! ❤️

We are so grateful to everyone who entered January's giveaway and can't wait to do it again in February. Follow us on fb and Instagram and watch for our next giveaway!

02/01/2021

I haven’t been feeling well the past couple days so I thought it was about time I went on a run🏃🏼‍♀️! It always makes me feel better 😊
I’m also just sticking to some grapefruit with coconut sugar for dinner but I’m oddly happy with it 😋

@ Alamo Springs Ranch, Fredericksburg, Texas

01/26/2021

**GIVEAWAY!!!**

Since Covid has delayed the opening of Camp Diasozo, we have decided to make a $100 contribution for the month of January to a family with a child who is living with scleroderma or morphea. If you or someone you know has a child with scleroderma or morphea, tell us briefly about the family or child in need and pm us with the family's name and contact info by Friday, January 29, 2021 at 10 p.m. central standard time. We will choose a winner from the submissions and announce it here over the weekend!

12/31/2020

A little bit of Texas snow to ring in the new year!! ❄️

12/30/2020

Time to stay hydrated!! Apparently my red blood cells are high so here’s hoping that I was just dehydrated! 🤞🏻

11/22/2020

We're so happy to partner with to bring awareness to this disease. Who do you know who has been affected by scleroderma??

11/15/2020

We here at Camp Diasozo have had the privilege of knowing Cat for a few years now. She and a handful of other young women battling scleroderma were instrumental in giving Shannie the confidence to embrace her lot in life and be who she is, unapologetically.

Cat was diagnosed at 22 and now at 33 her life here on earth is coming to an end. Her hope is to make it through the holidays with her family. Cat's mom, Sally, has willingly sacrificed so much to care for her daughter over the years, something that hits so close to home for those of us caring for our own sons and daughters with scleroderma. Please keep this sweet family in your prayers and help if you can. Their faith is extraordinary and something to be emulated. To God be the glory for this amazing young woman. ❤️

In 2010 at 22 years of age, Cat Davis was diagnosed with rapidly Advancing Diffuse Systemic Scle… Melinda Sanchez needs your support for Cat Davis Bucket List