All posts by KarenVasquez

Yep. I’m Still Here.

Yep. I’m Still Here.

Hello! So…someone from a private healthcare referral service received someone else’s death notification from the VA, then reached out to Angela*, my home occupational therapy provider, and told her I had died. The good news is, I’m not dead. Like all my posts, this is another story about my personal experience that I hope will make us all better health care advocates for ourselves and others.

The VA Did Not Fuck Up
Whenever I talk about a medical mistake, it’s usually assumed that it’s a mistake by Veterans Healthcare. The VA did set me up with OT, but they did not call and notify anyone that I was dead. The VA informed Bob, an employee of a government contractor that refers VA patients to private health care providers about a death. Bob mistakenly thought the decedent was me.

How Did I Get Here? Dancing.
During a hospital stay in December 2021, Madison, my in-patient social worker concluded that I needed ongoing home occupational therapy. Madison had to send that referral to another department to determine if I am entitled to home occupational therapy. Once approved, my referral was sent to Bob’s referral service to connect me with an OT provider.

The provider sent a patient treatment manager, an OT named Emma, to determine the course of my treatment. Emma submitted the treatment plan, then another OT named Angela performed my treatment. In my case, I was approved for 10 visits, with a treatment plan of two visits per week, to be reassessed by Emma after all 10 visits.

I was frustrated that I would have to be reassessed every five weeks to determine that I had not somehow been miraculously cured. Through the years, I’ve had different partners but it’s always the same dance. Before I knew the dance, most practitioners dismissed my request for any type of preventive therapy for scleroderma. Before it became the public norm to encourage people with disabilities due to chronic illness to stay active, any occupational therapy to slow down the progression was considered a waste of money. It took a long time for me to find medical providers who would help and encourage me to live a fulfilling life that met my standards.

More for Context
It’s not that I would need OT twice a week forever. My goal is always to get to a spot where I need fewer visits. Why do I think that’s helpful? That’s how it was done in the second half of the 1990s for me through the Madison Wisconsin Veterans Healthcare System. Ever hear the phrase, “If you’ve ever been to one VA hospital, you’ve been to only one VA hospital”? It’s fucking mind-numbing how each state can have different policies for its VA healthcare system.

When I lived in LaCrosse, Wisconsin, I was allowed weekly occupational therapy at a private facility. Back then it was called Fee Basis, and it was god damn spectacular.

When I returned to California in 1999, I presented Debbie, the occupational therapist at the San Diego VA, my treatment plan from the Madison VA hospital in Wisconsin. Debbie determined that the cost of local OT therapy was a waste of government funds to delay the inevitable. San Diego and Loma Linda VA Healthcare System felt the same way. Now, I’m at the West LA VA and after fighting for decades, I’ve got the OT I need. Well, I did until my case was closed thanks to the death fuck-up.

Treatment Interrupted
When any kind of treatment or therapy suddenly stops, it sets me back in function and reduces the odds of my fingers recovering as well as they could have. It’s a domino effect. I subconsciously guard an injured spot only to become aware of it after getting an additional impact wound because I zigged when I should’ve zagged. Those injuries are painful and protecting wounds by compensating in other ways leads to additional injuries and infections. Once this domino effect is in motion, it’s as easy to handle as nailing Jello to a tree.

How I Dropped Off the Radar This Time
It’s easy to fall between the cracks when care suddenly stops. Frustration is overwhelming and there’s always a chance of a visit from the Crippling Depression Fairy. It’s happened to me a lot.

Here’s what happened this time. A couple of Fridays ago, my OT therapist Angela, tested positive for COVID. (I tested negative BTW) She had no symptoms, but my visits had to be canceled until Angela was cleared. They couldn’t just send out another because I had been exposed to Covid. A week went by, so I reached out to her via text to see if she had been cleared. That’s how I discovered my death had been reported.

Now, I’m into the second week of no treatment. I have yet to learn if the referral dance I mentioned earlier must start again. It could be one week or two, maybe a month.

So who is to blame? Is it VA Healthcare? Or the companies paid to manage my case? It’s neither and it’s both. This cluster-fuckery is baked into the design of our shoestring healthcare infrastructure. Screw-ups remotely related to VA services make it easy for public opinion to favor private health care over government-funded healthcare like the VA. If funded properly, VA Healthcare could potentially make a good model for universal healthcare or Medicare for all. But we can’t have that. A small percentage of Americans need to collect dividends for their big pharma and health Insurance stock in addition to those “life saving” stock buybacks.

Ever notice that screw-ups at VA hospitals are all over the news, but rarely from our private hospitals? That’s because private health insurance and private hospitals have bigger public relations budgets.

If government-funded healthcare like VA healthcare looks shitty all the time, and private insurance overshadows their medical and administrative fuck ups with celebrity spokespeople, sound design, puppies, and talks about bare-minimum services like insurance companies are benevolent and care, of course, health insurance-funded private medical systems look better. Health insurance is the biggest racket since self-check-out at the supermarket. Self-service checkout makes as much sense as paying someone else to gleefully paint their fence.

It’s simple. If we don’t fund government services like veterans’ healthcare, they don’t work. Unelected douche canoes like Grover Norquist want the government to fail and benefit their own personal gain. They actually brag about it. I don’t want someone fixing my car who hates cars. Things like this inhibit progress. Could you imagine if the stagecoach industry blocked progress in automobiles the way fossil fuel interests have tried to kill electric cars? Sure, it would create jobs for horse shit removal, but it still would stink.

Good Government Is Possible
In that poorly named but well-crafted BBB bill, there were some great changes for all American citizens regarding healthcare infrastructure, especially for veterans. But of course, a small majority in the Senate removed that. Elected officials who are supported by pharma and health insurance companies can’t make government-funded healthcare look like a good option to voters.

What if VA hospitals were not 50 years behind in improvements? What if there was an updated system for medicare that made getting treatment less financially painful? What if veterans everywhere got better healthcare? No way. If government services like Veterans Healthcare and Medicare are properly funded, how would Americans continue to remain divided thus continuing to vote against our own best interests?

You Have The Power to Help Change This
Next time you think about thanking me for my service, don’t. Thank me by voting for representatives who will legislate for veterans in good faith by funding veterans services over privatization. It will work. I’m exhausted, and it would be great if I didn’t have to fight for simple treatments that when denied kneecap my quality of life and cost taxpayers more money in the long run. If you want government services to work properly, especially for veterans, stop trying to make government so small it can be drowned. The only difference between the quality of Kaiser Permanente and VA Healthcare is their PR budgets.

NOTES AND REFERENCES

*The real names of professionals in healthcare in all of my posts have been changed for privacy and to assert the humanity of those who work as public servants and private company employees.

The “Healthcare” Blog Category Explained

The “Healthcare” Blog Category Explained

I created a healthcare category. Veterans’ healthcare & insurance-funded health care have a lot in common, so Voila! It’s all in one place.

I’m a 100% service-connected veteran of nearly 30 years. I have advocated for myself as both a veteran and private insurance-funded healthcare*.  

The only difference is that one healthcare system can pass laws to prevent treatment, and the other lobbies politicians to pass laws to deny services to their customers.  

My goal is to share my experiences to promote more questions that will inspire  Americans to ask a minimum of one of these three:

1. Why isn’t veterans’ healthcare adequately funded?   

2. Veterans have family and friends who die from inadequate health care*. Why aren’t all Americans getting the medical care and social services we need?

3.   How is someone with no medical training in diagnostic medicine paid to deny needed health care and treatments based on the best bargain in favor of insurance company profits? 

References
Grammarist, “Healthcare vs Health Care“*

Veterans Provisions in the Build Back Better Agenda

Welcome Back to The Mighty Turtle.

The turtle on a skateboard wearng a rocket symbolizes perseverance with a side of humor.
Perseverance with a side of humor.
And of course, the Turtle’s name is Ricky-Bobby.  

Hello, my name is Karen Vasquez.  In 1994 I was diagnosed with a rare progressive degenerative disease called, scleroderma.  I felt isolated, even in support groups and after the internet became a thing.  I thought no one could possibly understand what I was going through.  In 2007, I was diagnosed with sarcoidosis in addition to scleroderma and that opened my eyes to the similar symptoms experienced by people with different chronic illnesses.  I started talking to people with other chronic illnesses and people who don’t have an ongoing medical stuggle.  I found one thing that connected us all, grief. I may not know exactly how a person with Lupus feels, but I do understand their loss of function and/or abilities.  

Not only did I find grieving loss in common with others who had different symptoms and hard to pronounce names, but I also found grieving loss in common with people who did not have chronic illnesses. Sure, I don’t know what suddenly losing a job after twenty-three years feels like, but I do understand what it’s like to lose my thumb at twenty-five years old.  Yes, they are distinctly different devastating losses, but both trigger overwhelming grief. 
 The Grief Connection  
In college, I was introduced to two books; one in psychology class and the other in philosophy class.  They are The Five Stages of Grief and The Power of Myth.  The Five Stages of Grief,  by Elisabeth Kübler-Ross, is based on her studies of death and dying.  The Power of Myth is based on a six-hour conversation between journalist Bill Moyers, and author of The Hero’s Journey, Joseph Cambell at George Lucas’ Skywalker Ranch in 1998. 

Continue reading…