IYKYK A fun model I threw together super quick. Hope you all like it ;) Links in following tweet!

To anyone who is still on this platform...I'm going to be starting up streaming again tomorrow! BUT, it will be different...not so much 3D printing, more baking, cooking, and anything else I feel like with the random 3d printing thrown in. 🧁Since Valentines day is the end of this week, is there anything that someone wants to bake for their significant other that they would like me to make and go over? I'm open to suggestions, otherwise I'll just run with it! 🧁 😜

Well, due to some unforeseen circumstances we will be open for commissions if anyone is looking to get something 3D modeled. It will likely be @GarrettKearney doing most of them, if you need anything you can send me a DM and I'll send you the email to reach out to us! Thanks 🙃 P.S. If anyone is in need of a highly talented computer programmer/game dev let me know. Someone I know has a hot resume they could send 😉🤞

🎄 Hei Hei got into the holiday decorations!!!🎄 Files for 3d printing are FREE right now on my @Thangs3D page! (Link in my bio & attached tweet)

MY FAMILY NEEDS YOUR HELP!!!!!! A Message from my parents about my nephew.... 4 weeks ago our grandson Kase was rushed to children’s Nebraska after a CT scan in Kearney showed a brain tumor. Children’s Nebraska in Omaha was able to fully resect the tumor. Kase has recovered well from the surgery; however, the diagnosis we received this week showed the tumor as a high grade glioblastoma and to make it even worse it showed he has LI–fraumeni syndrome. Li–Fraumeni syndrome (LFS) is a rare, autosomal dominant, hereditary disorder[1] that predisposes carriers to cancer development. As a child and even more important a child with this rare disorder, he should be treated with proton radiation therapy. There are such few cancer centers that have this treatment available and we keep hitting dead ends.  It feels like we are struggling to find a facility to help get us the treatment for his specific LFS treatment approach. Every minute matters in stopping any remaining cells from growing.  These cells being treated in his brain with proton, versus photon, therapy significantly reduces his risk of a secondary cancer growing due to the LFS disorder. We as a family are reaching out with hopes that there is someone you might know that would know someone that can help expedite getting him to an oncology team of doctors and help us give him the very best chance that he can have. In just the few days since his diagnosis we have had doctors tell us it doesn’t matter which treatment he gets and others that have said it does matter. We desperately want him to have the best option to live as long and healthy as possible. We are being challenged with lack of consistency and poor communication and are looking to change this in some way.  We truly believe, and so does our Oncologist at Children's Hospital in Omaha, that his best option, and chance, is immediate proton treatment, since this drastically reduces the risk that secondary malignancy would grow. Or, that other forms of cancer would develop, which is what would be guaranteed to happen, if they proceeded with the photon therapy approach. We are asking you to help us get the word out. We are forever grateful for all the support our family has received already, but are asking for anyone that can help us get in touch with that one, right person, and we can and will be there immediately! Every child deserves the very best chance anybody can give them and we want that for Kase. We are continuing to reach out to cancer centers and trying to get a response but are not having much luck. With the urgency, it cannot be delayed any longer. Every minute matters. If you or someone you know can help us, please DM me and we will exchange information there. Again we want to thank everyone for the support and prayers our family has received and continue to receive. We are forever grateful for anyone that can help us urgently get the treatment he deserves. With our deepest gratitude Troy and Cindi Clayton

If anyone has experience or knowledge about high grade glioblastomas and any clinical trials or anything please DM me asap. I'm just trying anything I can for more info right now. Thanks everyone ❤️

I need some massive thoughts and prayers or whatever good juju you can send in the direction of my family right now. We really really need it. 😔❤️

♥️🧡💛Celebrate love! 💚💙💜 I have some fun Pride sculpts and a keychain up on my @Thangs3D page FREE! Grab them here: than.gs/u/28873 #3dprining #3dsculpting #prideforall2024 #Pride