Couch Potato Files Vol. 14

Happy First Day of Spring. Crazy that we’ve already made it to late March and that our hotter temps are already trying to show up here in Arizona. Please stay away, triple digits, for as long as possible!

This past Sunday, March 16, was two months since I started on this wellness path with my ma. In all honesty, it feels more like six months. The old saying time flies when you’re having fun doesn’t apply in this case. It’s more like time stands still when you’re dealing with anything in the medical industry and you have no patience left or never had it in the first place. 

It reminds me of when my pop had cancer and the eternity it took for my mom and him to get help at the VA hospital, especially when he was literally dying and the clock was ticking away. Have I mentioned what a shitty healthcare system we have? 

The moral of the current trajectory I’m on with my ma is be careful what you wish for. I wished for my ma to get better and to take better care of herself, only to discover the list of what needed to be taken care of was a mile long. It all really adds up when you haven’t seen a doctor in three decades. So we try to laugh about it, that she’s making up for lost time, while every doctor, nurse, therapist and specialist we see has their head spin when they see her list of ailments. It’s pretty remarkable she’s survived, as morbid as that sounds and is. The story you see around the web about the 100+ year old woman who drinks a Dr. Pepper a day and is still kicking reminds me of my ma. I bought her a shirt that says “Save Water. Drink Dr. Pepper.” for a reason. I took her a mini can every day to the hospital and I knew the days she was really struggling were the days she wouldn’t drink much of it. Same goes for at home now. 

In all reality, this dumpster fire of an adventure has been a real learning experience, not just about how cocky I can get with acting like I’m a nurse or doctor, since I’ve now read and experienced enough to maybe give nursing school a go or even med school – not really, just like to act like it. But, it’s more a learning experience about myself, my family, friends, and the medical industry. 

I’ve found that many can be empathetic or sympathetic and many are just assholes. I’ve learned that some people can’t dig in and help or even know where to start and that’s ok – maybe some just literally can’t and it’s not in their make-up as a human. Although it’s frustrating, I keep reminding myself that on a daily basis.

I also have learned that I don’t post on social media or write here on my blog to seek sympathy from others – it’s a coping mechanism since I love to write and this whole experience has given me A LOT of material. When I do finally take the time to book my own therapist appointment, I plan to provide whoever the lucky contestant is with the link to this blog. It’s the cliffnotes’ version of what they’re in for BUT they might also find some interesting TV and movie recommendations as a nice bonus.

This whole experience is still a giant PSA to take better care of myself and my family. There’s just no excuse and if depression takes over, seek help. I just really, REALLY wish my ma would have let me help sooner but there’s no take-backsies, especially when it comes to this shitshow of a situation – I’m just still so grateful I got to her before it was too late. And let’s be honest, it may be too late anyway but I’m glad she’s trying. Even as small as the improvements are every day, they’re still improvements. 

Couch Potato Files Vol. 13

I’ve had a Vol 12 doc sitting in my Google Drive folder for awhile. Someday I will get back to it and my usual fun recommendations for TV shows and movies. For now though, I have a special entry that I need to write as I sit in a hospital room with my ma for the fourth time in just under one month.

We’ve visited three ERs and hospitals since January 16th in both California and Arizona. Neither of us set out to make 2025 a big year of change but it’s turned into that, for better or worse. It felt like for the better until the last few days and this most recent hospital stay. 

For over thirty years, my ma hasn’t seen a doctor’s office or hospital for her own care and now is making up for lost time. She sadly didn’t keep up with regular check-ups and her health has taken a big decline in recent years. I have pleaded with her to see doctors and even have gone as far as to make appointments, only for her to stubbornly make me cancel them. In hindsight I should have not taken no for an answer but I really wanted her to care to seek help as much as I wanted her to receive it.

She spoke regularly of not wanting to be a burden only for me to then tell her she was being a huge burden by not taking care of herself and not letting me help her.

So here we are now, at Chandler Regional, for the toughest days she’s experienced so far.

She’s suffering from Chronic Leukemia, Congestive Heart Failure, some crazy painful wounds that a primary care doc was finally able to tell us what they were called and why they even happened and now a side fracture and head-to-toe sore body and pain from a scooter fall earlier this week. 

The hardest part is watching her decline in the last few days since she was pretty hopeful as of just last Thursday when she was discharged from a Colton, CA hospital and we drove home to Arizona, a move I’d been wanting her to make for over twenty years, after my pop passed away from throat cancer in 2003. That hospital had helped us with everything but the scooter fall and we were on a path to better days. Days that included her living with us and then hopefully by us with some assisted care, seeing her granddaughter graduate from high school in May and other fun family things that got her active again. She’d spent the better part of two years at home alone, not facing any of her increasingly evident medical problems. 

Ironically her recent scooter fall unearthed more problems than even the fall, underlying problems that she had been downplaying quite a bit and the heart failure has intensified too.

As much as I love my ma I am filled with anger and sadness for what has happened. Most of her medical problems are self inflicted or at the very least could have been more preventable or maintained and I can’t for the life of me understand why she was ok with suffering for literal years and not seeking any help. Her stubbornness and independence to live life on her own terms and not “burden anyone” turned out to be the worst route to take. And, I really don’t know if she’s even accepted that reality or is just angry with me for finally taking her down what she likely thinks is this unwanted hospital ridden path of pain. 

What I do know is that some therapist is really going to enjoy taking some of my hard-earned dollars very soon. I used to see a therapist when my pop passed away so it’s been awhile and it’s time to saddle up again.

As hopeless as right now feels while writing this, I do still hold out some hope that my ma’s health improves and she’s able to move on from this current hospital to a skilled nursing facility and rehabilitation center. I’m really hopeful she hasn’t given up because I haven’t given up on her.