adrian_turtle: (Dracomir)
I have carefully avoided eating in restaurants for more than 5 years now. I remember the last time I casually got a cup of tea and a macaroon in the library cafe (in early March of 2020. That was the trip where I checked out a doorstopper of a short story collection that sat on my headboard shelf for 10 months.) After the 3 of us were vaccinated in 2021, we went out for lunch, rejoicing. We didn't know how little help the vaccine was on somebody immunocompromised, nor how little it helped with the new variants. That was probably when Vicki got Covid. And pneumonia. And she's coughing yet.

For a long time, I've heard some people saying Covid has been thoroughly suppressed already and we can go back to doing what we like. The economy needs it, or everyone is exhausted, or it just isn't necessary to be cautious anymore. And I hear others say common courtesy requires stringent precautions: masking everywhere, not eating in restaurants, etc. Brunch? You would risk everyone's health for something as trivial as brunch? Yes, I am taking stringent precautions, but it's a loss. And it has been a real loss that I have not been able to have a festive meal in company. That I have not been able to invite someone over for dinner. That I have not been able to stop off for a sandwich as part of a long day of errands. It's not trivial. (footnote) I've missed it.

I spent most of last week at a shiva out of state, eating meals at restaurants. Cousins very kindly drove me everywhere, as I can't drive. There are restaurants that one or another of my relatives really like, so all eleven of us went together. Sitting under flickering lights, in a large group that contained Cousin Shouty, it did not seem feasible to keep my mask on OR ask detailed questions of waiters before each meal. Are the eggs cooked in butter? Is there beer in the fried mushrooms? I took a lot of LactAid, but it wasn't for dairy foods that I enjoyed. I ate in restaurants without masking, but they weren't foods that I enjoyed, and they weren't experiences that I enjoyed.

So now I am wearing a mask at home. To protect Vicki, in case I caught something from all that unmasked running around Ohio and eating in restaurants.



(footnote) I do eat outdoors in company in good weather, but I live in Boston and good weather for outdoor dining is not predictable, and just doesn't happen for much of the year. Especially for those of us who can't tolerate serious heat and don't have our own comfy backyards.
adrian_turtle: (Default)
I made a doctor's appointment yesterday, and the person in the office asked me a question I didn't expect. (No, I still haven't found a primary care doctor. Still looking.) I found a neurologist connected with MGH who seemed vaguely promising, so I called the neurology clinic desk at MGH. The nice person there arranged for me to have the next-available appointment with a neurologist she thinks might be able to help. I'll let you know in 10 months how it goes.

The person in the neurology clinic really was very helpful in setting up the appointment, and asked all the usual questions about name and address and insurance and emergency contacts and so forth. They had a more extensive form than I expected, either because it's 2025 or because it's such a big hospital.
Some of the questions are recognizably sensible even if I'm not accustomed to them. Am I looking for a second opinion? Am I being treated for this problem currently? Have I been hospitalized overnight in the last 4 weeks? Do I plan to arrive by ambulance?
Then they asked "In what state were you born?" This is not relevant to my health nor to my health insurance. This is not part of my medical records at all! It's on my passport, which I've never needed to show a health care provider or insurance company.

A neurologist once asked me if I'd been born by C-section, but I don't recall him asking where. I suppose it might be relevant to a person's brain chemistry if they had spent early childhood in some spectacularly polluted area. But that's a confluence of place and time, and the place is usually more specific than the whole state. I was born in Michigan, but I left long before the notorious water pollution of Flint. I was even out of state the year half the milk was contaminated.

I vaguely recall hearing that in some states (Texas? Someplace else down south?) there were new rules last year requiring hospitals to ask patients their citizenship status. Could this be that sort of thing? It hardly seems plausible. If Boston's major hospitals closed their doors to everyone who had been born abroad, all the places would collapse.
adrian_turtle: (Default)
Well, that was a waste of time. I put so much time and energy and worry trying to find doctors in the Aetna directory that were listed as being near transit, listed as taking new patients, and listed as affiliated with the appropriate hospitals. As I said in the last few posts, I ran into an awful lot of trouble with doctors being covered, but working in hospitals that were not covered. Then I found hospitals in the network, but doctors working in them were out of the network.

It did not occur to me that Aetna would mark doctors as "taking new patients" when they did not. The information looked so plausible it did not occur to me to question it. Like, one doctor's office has 4 doctors and the network says 1 is taking new patients. Or a big clinic has 14 doctors and 6 NPs and 8 are taking new patients. And I finally find somebody I want and call to talk to the New Patient Coordinator, who tells me none of the primary care providers associated with their hospital are taking new patients. None, at any location. The wait list is closed. She suggests I call back in 2 months.
adrian_turtle: (Default)
I am in search of new medical care. I am not dangerously ill, but I'm not healthy either, which is probably a good time to be going about it. I found a doctor 3 months after moving to Massachusetts, Read more... )

I'm looking for a primary care doctor and a neurologist in the same hospital network, all 3 covered by my insurance. If I need an EEG or something else they do in a hospital, I want it all to be covered. I didn't expect it to be so hard. Read more... )

I have 2 searchable indices. I have a map. I have an insurance company that actually answers questions over the phone. Why the hell is this so hard? It can't be good for my blood pressure.
adrian_turtle: (Default)
This morning, I was running a small errand at the doctor's office. It was just an errand, I'm not sick, so of course I waited while they dealt with other people. A family having a Bad Day came into the waiting room from the doctor side. The mom was carrying a child of maybe 8. They were the size of big kid you don't carry unless something is wrong, and it's a long way down the hall to the elevator. There was a little kid (2 or 3) trailing along behind looking worried.

I stood up and offered to get the door to the hallway for her, because she had her hands full. She said, "Oh no! Thank you, but I don't want you to get sick. I can get it." I was wearing an N95 face mask. She and her sick kid weren't. I want to appreciate her kind thought, her desire to protect a stranger. I just wish we lived in a world where such kindness was more usefully expressed.
adrian_turtle: (Default)
Last week was difficult, as everyone knows.

So then Monday morning I went into the dentist's office for some minor oral surgery I had been very carefully not thinking about because otherwise I would panic. And the dentist said it went well and I am taking it on faith that it went well and my feeling that something is terribly, terribly, wrong is all in my head only in the sense that my jaw is in my head and has not healed yet.

And I tried to make applesauce Monday afternoon. I have a peculiar sort of plastic bandage inside my mouth on one side, and instructions to eat on the other side. And not to eat anything hard or crunchy. We had plenty of apples from the farmers' market in the refrigerator, but I didn't want to take expensive apples with delicate flavor and good texture and cook them down to mush, so I got some from the store. They had quinces next to the apples, and I thought it might be a good idea to throw one into the applesauce. I had one of those steel things that cuts the core out of an apple or pear and divides the fruit into 8 pieces with a satisfying ker-THUNK. I took it home when we were cleaning out the synagogue attic last year, and enjoyed using it. Alas, the quince was stronger than the kerthunker! The outer ring tore away as I pushed it down, so the jagged ends of the spokes cut me. It wasn't bad enough to need stitches but it was still very upsetting.
adrian_turtle: (Default)
This is not the future I expected, back in the 20th century. Yes, I thought I might have an alternative lifestyle that my mother would disapprove of. But I didn't expect she'd disapprove of my getting vaccinated against contagious diseases. Or getting part of my electricity from wind and solar.

She doesn't understand about being bisexual and polyamorous, but she is ok with "these wonderful people are very important to me, and I am living with them now." I don't expect her to object to my rainbow-striped airgami because of the rainbow stripes. She just thinks it's dangerous to wear any mask and I should stop.

new iPhone

Jun. 10th, 2020 01:21 pm
adrian_turtle: (Default)
I have a new iPhone. I hate it.

It's not that I loved my Android )

Rather than live 2 weeks without library books on my phone, I bought a new phone. Wouldn't you?

So I have a shiny new iPhone SE, which seemed to be the smallest thing on the market. Does everybody actually want such big phones? Doesn't anyone put them in their pockets anymore? I don't want to play video games, and I resent that it takes a more and more powerful phone for me to get real time information about bus connections and when somebody is looking for a math tutor.

It's big and heavy, )

It's hard for me to read. )

Even though it's 3 kinds of physically painful, I'm afraid I'm stuck with it. Apple would probably be willing to take it back, because I only got it yesterday. The problem is that any other machine capable of running the apps I want would be even heavier. I would be happier about trying to work with the damn thing if it would do what I wanted in other ways. I have a lot of epub and mp3 files on my Android, and I can't figure out how to transfer them to the iPhone. Is this even possible?
adrian_turtle: (Default)
I don't mean "why am I on Dreamwidth?" I'm HERE to stay in touch with the rasff diaspora and its friends and relations.

The question is "Why am I living next to Boston?" and the answer to that is that it's a city where people live fairly close together, and I can walk to many of the places where I want to go and take public transit to others. I can be welcome in several overlapping communities. There are lots of people I don't really know, but we smile and nod and say good morning at the bus stop or passing on the sidewalk. I feel surrounded by a vague network of friendliness in a way I wasn't, where everybody traveled by car.

In other words, I love this city because it's a place where large numbers of people breathe on each other. Oops.

ginger ale

Aug. 23rd, 2013 02:36 pm
adrian_turtle: (Default)
A few years ago, Coca-cola started advertising that their new cans of regular coke contained only 100 calories. They had reduced the calorie count by making the cans slightly smaller--it seemed like a nice thing to do for their customers who liked the taste of classic coke and didn't want too many calories.

A couple of days ago, I was on an airplane, and I asked for ginger ale when the flight attendant offered me a drink. I hardly noticed the little green box on the green Seagrams can, announcing "25% fewer calories than regular ginger ales." When I saw it, I thought maybe they were using less sugar--a less sweet ginger ale would be nice. (There's a version of frosted flakes that just uses less of the frosting and brags that it's a lower cereal.) Then I thought maybe they were using a smaller can, but the can had a weird aspect ratio, and I picked it up trying to read the label to see how small.

It was a little tricky to read the label, because I didn't have my reading glasses. (I just had my e-reader, which lets me use big fonts and my distance glasses.) So there was a fair amount of dumb luck involved in seeing the sucralose on the ingredients list in the first place.* It wasn't diet pop; it had lots of corn syrup. It felt like they were just sneaking the migraine trigger into the can and hoping people wouldn't notice.

They really are being sneaky. It's not just that I was oblivious or that I've had so little ginger ale this year (while irrationally thinking of it as a familiar product I don't need to investigate before drinking.) I went back to the little airplane galley to discard the unused can and see if they could spare me a little water, and the flight attendant was shocked. "What seat are you in? I could have sworn I gave you regular soda!" No, really, it's not her fault. It looks exactly like non-diet soda. By the standards of people who want the diet stuff, it probably IS non-diet soda. Seagrams is just being sneaky. Or I suppose a person could use a less polite word than "sneaky."


*The flight attendant gave me the can in the first place, instead of just pouring me a cup.
I noticed the green-on-green box.
I read the ingredients list, when I didn't expect any need to.
adrian_turtle: (Default)
I went to see a new medical specialist this morning.

Office Manager: And what's your primary care doctor's name?
Adrian: Doctor [name]. It's spelled [...]
Office Manager: Do you know his first name?
Adrian: Of course. It's Deborah.

The office manager was seriously flustered by her mistake. I'm wondering how, in 2013, she might have made it. It's not like it's UNUSUAL for a family practitioner to be a woman. What surprised me even more was her thinking that I might not have known my doctor's first name.

A long time ago, when I lived in Michigan, my doctor was Dr. Bernstein. He shared an office with Dr. Blum, and I went on seeing Dr. Blum after Dr. Bernstein retired. I think I had some abstract awareness that they must have first names, but I had no idea what they might be.

Is this a difference between the 1970s and now? Or between how children and adults interact with their doctors? Or is it not perfectly routine to know the first name of one's primary doctor?
adrian_turtle: (Default)
The word "opiate" does not mean "something that makes a person behave badly." It does not even mean "something that makes a person behave badly, and is also hard to stop using." Most especially, it does not mean, "something that makes a person agitated and short-tempered, and is hard to avoid because it's so pervasive."

I wish there was not so much stigma around the medicine that lets me be as functional as I am.
adrian_turtle: (Default)
As many of you know, I live in Massachusetts, which has had a patchwork of nearly-universal health insurance coverage for several years now. We have religious exemptions to our health insurance requirements, but it's not nearly as infuriating as the type being discussed in national politics these days.

The Massachusetts plan tries to get as many people as possible into insurance plans, considering different reasons for doing without insurance:
1) health insurance plans won't sell to them
2) they have access, but can't afford the premiums
3) they have access and money, but want to save their money because they don't expect to need health care this year
4) they object to seeing doctors, on general principle

So there are rules for the health insurance plans to address problem 1, that they have to make their plans available to everybody, and can't raise the premiums too much. And rules for businesses, that they have to make group plans available to their employees. And subsidies to help low-income (and moderate-income) people with premiums. It's a reasonable attempt to address problem 2. In an attempt to get the 3rd group to pay premiums (whether they get insurance and health care or not), you're supposed to pay a tax penalty if you opt out of buying health insurance for reasons other than low income or religious conviction. The penalty money goes to support the subsidies.

The 4th group doesn't involve all that many people, but they're symbolically important. I don't know what religions have such strong objections to all medical care that the devout consider it wrong to have health insurance. (Maybe Christian Science?)

My Massachusetts tax form asks:
Are you claiming an exemption from the requirement to purchase health insurance based on your sincerely held religious beliefs?
If you are claiming a religious exemption in line 8a, did you receive medical health care during the 2011 tax year?


It was a religious exemption for individuals wanting to avoid buying health insurance. When did "religious exemption," in the context of health insurance, start to be about employers or insurers wanting to limit coverage? I feel like the jargon changed under my feet, and I didn't even notice it had changed until I sat down to do my taxes.
adrian_turtle: (Default)
Last month, I posted about a medical procedure I was planning to have on December 16th. It was scary and expensive, but I was hoping it would stop my migraines for a few months. I knew it wouldn't be an immediate fix. Patients who have good results report some pain after the injection, even headaches as a side effect. And the good results don't happen for at least a week. The doctor told me to expect optimal relief beginning 2 or 3 weeks after the injection.

I have mixed feelings about this "optimal relief."

The first week after the injection was very, very, bad. The shoulder pain flare was spectacular, and referred to hand and jaw. And my headache got worse. And a lot of my coping mechanisms stopped working, because I couldn't use my shoulder. (This made me overuse my bad hand on the other side, which wasn't any good for me either.) Fortunately, the worst of that effect was temporary. My shoulder pain is back down to the level it was in early December, with a reasonable range of motion. The problem is that I can't lift much at all.

You might have thought I couldn't lift much before. I certainly complained about not being able to do the hands-on part of my work in materials engineering. I was unhappy about not being able to carry a preschooler, or a whole turkey with a lot of vegetables. It's different when a 5-lb bag of oranges, all by itself, is too much to carry home in my backpack. It's different when it seems prudent to return paperbacks to the library one at a time.

For all that, it DID help my headaches. I had a continuous migraine from 10/29 to 12/29. Since then, my migraines have been frequent, but not continuous. I've even had a couple of half-day intervals with no headache at all, which were just lovely. That hasn't happened since the summer of 2000.

Thus, as I said, mixed feelings.
adrian_turtle: (Default)
Strobes don't bite most people, so he can get away with that. Usually. Last weekend, it went bad.

I was uncertain about going to Chicago for my cousin's bar mitzvah. I thought it would be worth the strain of air travel to see that set of relatives* and maintain my connection with the family. What really worried me was the possibility of strobe lights at the party after the service. Strobes are the worst triggers for my seizures, and pretty bad migraine triggers as well.

I dithered for WEEKS. It would be an evening party, which made strobes more likely. Yet it was a party in the synagogue social hall, which might make it quieter and less likely to have strobes than a party in a more party-specific space. Last time I saw the bar-mitzvah boy, he had been a very young 12 year old...would that make him less likely to be interested in the kind of dance party that relied on strobes? The next older cousin (who'd had strobes at her bat mitzvah party, that kept me hiding in the lobby most of the afternoon, and still needing a week of recovery time afterward) seemed a lot more sophisticated.

I finally phoned my cousin** and asked him if there would be strobes or flashing lights at the party. I grew up with the idea that it's an outrageous imposition for me to ask somebody to turn off a flickering light, or not to wear perfume. Now, mostly, I can recognize that people outside my family are ok with such requests (and if they aren't, I can walk away.) But when dealing with relatives, I can't bring myself to ask them to change what they're doing for my comfort. It feels daring and rude just to ask for information, so I can be be elsewhere if I think it's going to be too uncomfortable.***

In this case, my cousin was very gracious about it. He said they'd hired a DJ, and didn't know if he would have strobes. He's be happy to ask the DJ not to use any strobes, if they were a problem for me. I made travel plans thinking that maybe it was no longer appropriate for me to go on defining that side of my family based on my mother, my aunts and uncles, and my grandparents (of blessed memory.) The kids' table takes over gradually, and I didn't notice a lot of it, because it happened between my aunt and my cousins.

I shouldn't be surprised my cousin was so gracious about this issue. We haven't spoken much in the last few decades, and weren't particularly close as children, but I have no reason to think he's a mean guy. And I wasn't thinking about it when I made the call, but he has some reason to be sensitive about this sort of thing. The bar mitzvah boy also has absence seizures, and his parents have spent the last ten years trying hard to protect him from possible triggers. His seizures are very infrequent, and he's not photosensitive, and of course parents are more protective of children than adults are protective of themselves. Even so...when they're trying hard to make sure the kid doesn't have a seizure the week before he has to do something important, I wonder if my attempts to insist "I'm fine, it's nothing," for only one seizure in an evening might be inappropriate.

So. There I was, after the service, in the lobby of an enormous Chicago synagogue. The doors to the dining room were open, and the music was starting up, and I could tell there were strobe lights. Not a single device like a photographer's strobe, or even a disco ball, that I could point to and say "please turn that off." It was a whole dramatic light show, with flickering screens in several colors. I decided to stay in the lobby, eat the appetizers being carried around on trays, and play with my little nephews and their toy trains. (They didn't like the light show, either. Or possibly the music or the crowd.) It was unfortunate to miss the party after coming all that way, but the appetizers were yummy and there were lots of them, all pareve. And my nephews and I were enjoying one another's company. And maybe I could chat with various other relatives in passing. Everybody went in to dinner, and I settled down in the lobby.

Then my sister-in-law came for the boys. They had to go in and eat dinner. "Oh, you can't stay out here and miss the the whole party!" I tried to explain. A cousin came out to chat, and to invite me in. "But they turned off the strobes! You have to come in for this part!" I explained I preferred to stay in the lobby. Eventually, I was convinced to go into the party space--just for a little while, you'll see how safe it is now, it won't bother you, you really can't miss this. It was my own bad judgment that made me go into the room. But I stayed in the room for 2 hours because my judgment was so badly impaired by frequent seizures.

I made it home with great difficulty. I've felt purely awful all week. I am recovering, albeit slowly; I couldn't have written this on Wednesday.



*I would be seeing my brother and his wife and children, all my cousins and aunts and uncles on that side of the family, but not my mother.

**the one whose bar mitzvah was in 1980, not last week. Now that I think of it, that one also had strobes that made me uncomfortable, though it wasn't nearly so bad.

***as the bar mitzvah last week was Saturday evening, the young man was talking about Lech Lecha. He spoke of how admirable it is to just *go* when told, rather than trying to negotiate. (You want me to go WHERE? What's so great about this land that you will show me?) It echoed through what little thinking I was doing, later in the evening.
adrian_turtle: (Default)
Elise had a stroke a few days ago.* She managed to communicate enough of the problem that the person with her (sensitized by having one dear friend recovering from a stroke, and another working in emergency medicine) recognized the emergency and called 911. This was all despite Elise's initial desire to lie down and hope the symptoms went away. Thanks to prompt treatment, the stroke did not do permanent damage.

Elise, and the many people who care about her, bounced from profound terror to profound relief. In the first day or so after the stroke, I saw several people posting the news that she was in the hospital, and there was a tremendous outpouring of sympathy and offers to help. From over here, it looked like caring for Elise, caring for the community she helps build, and an attempt to fight back against disease and feeling helpless. Now that Elise is back from the hospital, and her stroke is no longer a medical problem, the community is redirecting the desire to help. I understand why so many people are talking about the importance of calling emergency medical services at the first sign of stroke symptoms. I even understand why the conversation has such emotional intensity--all that energy from fear and relief and the sudden transition has to go somewhere.

It's still making me uncomfortable. Read more... )
adrian_turtle: (Default)
I do not want to see this correlation, because it makes no sense and because implies I should limit my already limited lifestyle in fairly unpleasant ways, but here is the suspicion. It looks like audiobooks are bad for my shoulder. (Books or music. Any mp3 I listen to on purpose. But in practice, it turns out to be mostly books.) I got out of the habit of listening to anything after I got my ears pierced, but went back to it in January.
adrian_turtle: (Default)
I went to the eye doctor last year, and determined that my glasses prescription was a little too strong. I hadn't been sufficiently aware of this for it to send me to the eye doctor. I went because I was seeing bugs that should not have been in my apartment, that should not have been on my PLANET. When I asked the doctor who prescribes my anti-seizure meds if perhaps my brain might be playing an unpleasant new kind of trick on me, he asked if the bugs tended to turn up in the same place, and where I was when I saw them. When it turned out that I was seeing them in different rooms, but always to my left, he sent me to an eye doctor. My eye playing tricks on me is very much less scary than my brain playing tricks on me. The eye doctor assured me that I was seeing a moving dark spot and just interpreting it as "bug," and that it would gradually get smaller and disappear. That's how it went, from Lovecraftian horrors to palmeto bugs to ladybugs (a few of which I could see with both eyes and even step on) to ants. And no bugs at all since the middle of December.

I've been getting less nearsighted as I age*, rather than the more common pattern of becoming both nearsighted and farsighted and needing bifocals (or transition lenses. Or two pair of glasses.) I know some people have a lot of trouble adjusting to bifocals or transition lenses, or are unable to do so at all, and I'm afraid I might be one of them. I have been really, really, bad at visual processing since I was very young and throwing up every time I tried to use a Viewmaster. This past eye exam included something I've never done before--I don't know if it's a standard thing for being over 40, or something this doctor does, or a recent part of the standard of care. After I looked at the eye chart across the room, with and without my glasses, the doctor gave me a laminated card with an eye chart on it, and told me to read the smallest line I could see clearly. "Where should I hold it?" "Wherever you like. Any place that's comfortable for you to read it." So I held it about 18-20" away and read a line with my glasses, and she asked me to read the next line but it was too blurry. And I took my glasses off, and had to move it closer because I couldn't see the text...but she'd said that was ok. At about 8-10" from my face, it popped into focus. Even the small text I couldn't read with my glasses popped into focus. I wouldn't have believed it if I hadn't seen it with my own eyes, and I wouldn't have thought to do the experiment. 8-10" is a great distance for reading a paperback in bed, in case you were wondering. The eye doctor wrote me a prescription for new glasses, and advised me to take them off for reading fine print or doing close work. And she warned me that I am likely to need bifocals or transition lenses in a few years, but that they are likely to be problematic for my migraines and motion sickness so I should put them off as long as I can.

I remember when my glasses were -8.00 and -7.50, and I had to argue with the opthamologist who couldn't believe a 10% change was significant enough to cause eyestrain. (I suppose one might not notice a 10% change in a 1 or 2 diopter correction.) That transition was really brutal, partly because I was working a full-time job with a fair amount of physical danger, and my migraines were completely out of control. Now I'm going from -5.50 to -5.00 and -4.75, with more astigmatism correction. It should be a piece of cake. Furthermore, I'm home, and can handle the adjustment period in relative safety. I think it also helps that I have more faith in the ophthalmologist. Anxiously second-guessing whether the new glasses are really a good idea makes it harder to persist through the headaches and double vision and motion sickness. This is going to be easy. Right. Easy. I am still going to go lie down for a bit.



*Note to the opthamologist in Winter Hill: this is unusual. It is not unheard of.
Note to the optometrist in Porter Square: this is unusual. It is not freakish.
Note to the medical professionals of the world: if our bodies worked perfectly well, we would not be consulting you nearly so often. Please be respectful of the ways in which bodies work differently or fail to work. It is your job to know this stuff, for crying out loud.
adrian_turtle: (Default)
A few weeks ago, my doctor suggested trying a new kind of treatment for the chronic pain in my hand and shoulder. It's not the silliest thing I've ever heard of, but the competition there is pretty stiff. A low intensity laser tuned to exactly the right wavelength is supposed to stimulate the mitochondria to produce more ATP, which improves healing even in an old injury. What amazes me is that this therapeutic wavelength is VISIBLE light. I don't see how it can get past my skin to the damaged tendon, much less reduce the scar tissue on the other side of the tendon. I want it to help. I want so much for it to help. And I want a hypoallergenic pony unicorn.

I tried it once, for both hand and shoulder. It didn't seem to do anything for the hand at all. It might have helped the shoulder a little, briefly. It didn't do me any harm, which puts it way ahead of lots of other pain treatments (including massage, direct acupuncture, capscicum ointments, muscle relaxants, and almost all PT.) So I tried it again, just on the shoulder. Again, it might have helped a little, briefly...I can't tell if it's a real benefit, or if I'm fooling myself because I want it so much. The pain varies so much it's hard to be sure of changes when they aren't large, sudden, or consistent. Did it get better because of the treatment and worse when the treatment effects worse off? Or just a little better in the warm middle of the day and worse when it got cold at night?
adrian_turtle: (Default)
Dear Health Connector,

Thanks for running this contest, asking people to tell their stories about why they are happy to have health insurance. I think it's great to have a wide range of personal stories as well as financial statistics to show why health insurance is such a good idea. I won't be entering the contest myself, though. I wouldn't, even if I really wanted the Red Sox tickets you're offering as a prize.

If I didn't have good health care, I would be so disabled by chronic pain and depression that I couldn't work at all. Thanks to the Health Connector, I have been able to afford health care when I was looking for work, or working intermittent contract jobs with no benefits. That makes me healthy enough to work 40-45 hours/week, doing the kind of scientific work I was trained for. Unfortunately, chronic pain and depression are both heavily stigmatized. Many employers would rather not hire somebody with that kind of problem, even if it's controlled well enough to not affect job performance. I don't want you to publicize my story, because I rely on medical privacy to protect me from discrimination.

I expect you'll get stories from lots of people whose lives were saved by health insurance. Or their children's lives. Stories of life and death are certainly dramatic, and a program that saves lives is impressive. But I wonder how many people are using health insurance to stay on the employable side of marginal disabilities? (Is the state as a whole supposed to turn a profit? Or is it just health insurance that is supposed to take in more money than it spends?) Those people are tremendously happy to have health insurance, but they aren't going to tell you about it, if they are trying to keep stigmatized disorders hidden.

Best wishes,
[name withheld]

ETA: Hours later, I noticed that I wrote "those people" to refer to a group that includes me. At the end of a letter *about* being a member of that stigmatized group. Speaking of stigma.

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