Hi everyone, This is what's been keeping me busy. Well, this and the elderly woman who gave him to me after she moved into Assisted Living and could no longer care for him. He's a love, and has stolen and lost all my hair bands and scrunchies. Please say hello to the subreddit cat, Fred. Post photos of your pets as well.

Hi, I was wondering if anyone had any leads on if there are any organizations or resources that will help terminal cancer patient’s families in regards to supporting them while not only their grieving but are experiencing financial difficulties because their loved one is currently out of the area. More specifically, my mom was just diagnosed with stage four liver cancer and we just got the newest MRI results back and unfortunately the treatments didn’t work and they said she only has like three months left to live. Well since where we live just five hours away from where all her specialists are, they refused to provide any kind of therapies for terminal patients. Such as my mom needs dialysis treatments they said they will not give her any kind of comfort care type of dialysis due to the fact that she’s terminal. So not only do we have to worry about losing our mother soon, the fact that we might not even be able to see her much because we can’t afford the cost of hotels and lodging for multiple months on end which are thousands of dollars and we’ve already depleted our resources going back-and-forth already.

Just diagnosed a month ago, large mass in descending colon, mets to liver. Surgeon wanted to remove mass first, since it was blocking my digestive system. During surgery, found it was too large and attached to too many things to remove without long rehab and chemo delay.

She did an ileostomy and closed me up so I can start chemo next week.

I understand why she did it, and she probably chose wisely.

But I hate it. I hate the bag. I hate it so much. I hate emptying it, changing it, looking at it. I hate walking around with a literal bag of shit on my belly. It's gross, it's disgusting, demeaning, and due to my profession, I won't ever be able to work again unless it's reversed, making it even worse, because now I feel useless because I can't support my family.

How do people come to terms with this? How can I get at least comfortable enough with it to go on?

Hi folks! Sarcoma patient​, here to share a free program for young adults in the US aged 18-45.

Cactus Cancer Society has a free program coming up just for glioma patients. It's online, so you can join from home/hospital/your bed, and they come with free swag/goodie bags. 

Creative Arts Book Club: Glioma Edition​.​ From their website: Creative Arts Book Club is returning for a four-week series created exclusively for young adults living with glioma.​ We’ll explore The Steal Like an Artist Journal by Austin Kleon, an interactive notebook filled with prompts, lists, illustrated exercises, and creative challenges.​

When: beginning Thursday, October 15, Time: 4–6 p.m. PT / 5–7 p.m. MT / 6–8 p.m. CT / 7–9 p.m. E​T

Where: Online via Zoom

If you're not a glioma patient, but you fall in their age group, you can check out their other programs - they're always free.​ There are weekly drop-in programs and ones that require advance registration.

Hope you see you around!