Can’t seem to get med refills or doctor appointment before leaving town. They interrupt and don’t listen to you. I even got hung up on trying to explain why people with autism hate talking on the phone and why it’s such a problem for a supposed mental health provider. Hardly any locations in the city or accessible without a car. I don’t know if I’ll be in drug withdrawal for the two weeks I’m in Columbus. This is how Medicaid and King County Community mental health work. Programs for the poor are poor programs.
For all the bullshit about sleep “hygiene”–as if it’s an issue of cleanliness or moral weakness–it seems bloody obvious that sleeping in a different place every weekend with different animals, noises, beds, etc. is one of the MOST disruptive things you could do to your sleep. I’ve been pet sitting for 3 1/2 years, but not one health care provider pontificating at me about sleep has bothered to consider that. I need to be at home. Which means I need a different source of income. Which should be SSDI, but you can die waiting for that. I just managed to summon all the energy to arrange a trip to Florida; I’m in no position to fight the disability denials or start something like online editing for hire. I need someone to help me with that stuff, the energy of initial startup, but that would require them to be paid for their time. And a minimum wage sure as hell won’t do that, no matter how high or low. But situations like mine are invisible to those who choose a solution based on ideology, insist it’s perfect and ideal, and blind themselves to the human suffering it causes. I’m just collateral damage.
I saw a doctor and got temporary psych med prescriptions. I’m waiting for them to be ready. That should bring some relief by tonight. This doctor wanted me to alter an existing appointment, I forget why, so I go back Friday to see the kind, understanding, pretty doctor (locum) again. My regular doc is back soon, so she’ll be gone.
Today’s doc was naturopathic and suggested cranio-sacral therapy (?) for PTSD in Wallingford. I’ll look it up. She says they found a way to get Medicaid to cover it. She also wants to believe my toe numbness is due to high blood sugar, but I’m seeing diabetics online who have the same side effect from the med I take and say it goes away as soon as they switch meds, so I want to try an alternative. I’ll try to do the intake for longer term psychiatry tomorrow.
A small present I got myself arrived, so hopefully I can get the broadcast TV channels well and watch Jeopardy regularly.
I got an email blast from a temp agency I worked for years ago, seeking an executive assistant. They’re interviewing me Monday morning. I expect absolutely nothing out of this. They treated me pretty badly in 2012-13 after I did a great job for them in 2011. I mentioned the idea of unionizing temp workers, and they banned me from their Facebook page. It rubs me the wrong way that they’re even open on MLK Day, let alone having people interview then.
I emailed a bunch of information to the community mental health ombudsman, and he claims interest in helping but won’t deal over email. I’ve emailed and left phone messages for Larry Gossett about a few things, but the man never answers. I’m ready to vote for someone who responds to constituents, rare as that is.
So call this all cautiously relieved. Never count your chickens before they’ve hatched.
UPDATE: Two meds filled, one not ready until tomorrow.
We have a problem. Twice in the past month, my apartment has lost heat. Both times, I called DCI and filed a complaint. The first time, I never heard back from them, and my landlord, SHA, took five days to fix it despite the legally required 48 hour response time. They acted very non-chalant about it, saying it could take much longer, and there was nothing anyone could do about it, so I should just be patient. The second time, when I told SHA, I warned them that they faced citation and/or fine if they didn’t fix it in 48 hours. I didn’t hear back from DCI for five days. This time, SHA found the ability to fix the heat in 48 hours.
But in neither case did DCI even inspect my apartment. In neither case did they respond within the 48 hour limit. They never contacted SHA, so the 48 hour clock never started ticking. Had I not gotten lucky, there would have been no enforcement of the law whatsoever.
I fully expect my heat to go out again this winter because SHA is cheap and values nothing less than their disabled, impoverished tenants. I highly doubt they fixed the heat any more than necessary to keep it running a couple more weeks. I shouldn’t have to take my chances with DCI. They are not doing their job or enforcing the law. With no enforcement, tenants don’t really have any rights. And I’m one of the lucky ones whose native language is English, who can write articulately, who doesn’t have to worry about deportation, who knows my rights, who has professional experience working in housing and homelessness, and who can make savvy decisions about what scares landlords into following the law. This is totally unacceptable and even immoral. Please help.
What tenants really need is the no-brainer right to repair and deduct. It works, and it gives renters some agency over their own living situation.
[Written to Seattle Councilwoman Lisa Herbold, Chair of the housing committee and huge help to tenants in her district or not; my own Councilman Bruce Harrell couldn’t care less]
Please sign this petition against 2nd class transit. Here are my comments:
ORCA Lift is a great program, and I commend you for taking the leadership to implement a low-income fare in a major jurisdiction like King County. As a transit junkie and advocate, I know there are many good reasons for shifting fare collection away from paper and toward smart cards. One of these is the ability to create just about any fare category you want, and charge it to targeted populations. So I’m interested in working *with* ORCA rather than seeking a step backward (in the long term) toward paper fare media.
I appreciate the rationale for peak-hour and two-zone surcharges; they make sense from a transportation perspective. And I understand the reasons for having senior, disabled, and youth fares too–I use an RRFP myself. But it seems to me that these last three are indirect attempts to help people who really need it, which is mostly people with the least money. And a large share of peak-hour commuters paying both the distance and rush hour premiums are probably employees whose fares are subsidized by their employers anyway, so the surcharges raise more money but don’t have the transportation or location effects desired.
I increasingly believe that simplicity is of great and underappreciated importance, and income inequality nationally and locally has become so great that I think it’s now more important than the reasons for, and effects of, the rush hour and two-zone surcharges. So I propose that, short of violating any federal requirements, Metro end the surcharges, abolish the special senior, disabled, and youth fare categories, and charge fares entirely based on income. We have lots of good ways to verify income for people under 200% of the poverty line; we can use existing infrastructure to charge still lower fares for people below 100% and 50% of poverty. Above that, the County has a large role in health care, and the ACA offers premium subsidies to people up to 400% of poverty. I suggest that the Health Department, perhaps working with WA Healthplanfinder, use that information to verify incomes in the 200-400% poverty range and apply an appropriate income-based fare category. This would be simpler and fairer for everyone.