Disappointing Doctors, Villains, Notre Dame Review, and Looking for Fall
- At September 04, 2017
- By Jeannine Gailey
- In Blog
0
Hello my friends!
Notre Dame Review and a new poem
First of all, thanks so much to Notre Dame Review – I was so happy to get this acceptance after at least fifteen years of submitting – I received my Fall 2017 contributor’s copy the other day, including my poem “On Being Told You’re Going to Die, But Not Quite Believing It.” Here’s the poem and Sylvia posing with the Fall 2017 issue.

Villains and Disability
And thank you to Kelly Davio for her “reading loop” about disability and villains in pop culture, which features one of my poems 🙂 It’s also just fascinating to think about how the disabled body is often presented in movies and comics.
A Report on How I’m Doing, and Wishing for Fall
I’m sorry to report I’m not doing any better yet, especially after I had so many hopes for my appointment at the Swedish MS Center last week. The doctor was either extremely unknowledgeable or extremely uncaring (literally answering almost every question with a shrug or an “I Don’t know” – even for things that he definitely should have known something about as merely a practicing doctor, not to mention a neurologist )- or possibly both, and left me with no new information, no help for any of my problems, and a lot of frustration. (It was so bad I actually called back the office to complain, which I have literally never done before. They got me another appointment with a different doctor, but not til December. December!) If you remember my cancer stuff last year, you might remember I had a similar appointment with a “top” oncologist at UW, so I guess this is par for the course – you can never rely on the first doctor you see after a hospitalization, I guess. So I’m still unable to eat or walk much, mostly stuck inside, and frustrated by my lack of getting better. So many sweet friends have offered support, which I really appreciate, and at least my reading ability – which was knocked out by vertigo for a while – has some back, so I finished up work on a book review and my newest book manuscript draft and sent it in to a third publisher. (If any of you publishers are interested in a book about being diagnosed with terminal cancer and then MS, but you know, with a funny spin, please let me know. I could really use the pick-me-up!) The dizziness has improved with home therapy exercises but the nausea and gastroparesis stuff persists, unfortunately, along with the weird leg weakness and some other weird symptoms. I’m sorry I can’t report dramatic improvement yet, but then again, I’ve started no new treatments thanks to deadbeat doc neurologist #1, so…I guess it would be overly optimistic to hope this goes away on its own. But you can send good thoughts my way if you want, I feel so bad for my poor husband who has been taking care of me since a month before the hospitalization, just to watch me becoming increasingly sick and weak – I don’t like it, I wish he didn’t have to watch it either.
We have wildfires on all sides of us right now and they’re predicting weather in the nineties today and tomorrow. MS flares happen more often in the heat, so maybe things will settle down when our weather changes, at least I hope so. I’ve always liked the fall but never really craved it the way I have this year, this year of record-breaking heat and scorched earth and fires in the usually mild Northwest. Looking at the news – wildfires down the coast in California, Houston’s flooding, North Korea’s nuclear warheads – isn’t particularly hope-inspiring right now, is it? I’m hoping for something better for me, for the weather, for the world, soon. I think we could all use a break.
Still Summer, Still Struggling, MS Center Tomorrow
- At August 30, 2017
- By Jeannine Gailey
- In Blog
4
Hey guys, thank you so much for your support, which means so much in these long hot mean days of summer, which just keeps holding on, it seems. Just this week, I received a vase full of pink flowers from some of my speculative writer friends (thanks Nancy, Kelly, Lesley, Molly, Sally!), some really beautiful get-well-soon cards from various friends, an offer to visit which I hope to take on soon from one poet. I’ve ordered (on orders from occupational and physical therapists) a rollator/walker thing in pink, a pink travel chair, some “cooling” accessories, books on MS…a lot of fun shopping, you can tell. Apparently MS hits you harder when you get hot, so traveling with ice packs is a must, especially on these weird late summer hazy 90’s days we’ve been having. I’ve never been so ready for fall in my entire life!

I’m due at the MS Center tomorrow for my grand rounds and intake and such, and hoping against all hope I walk out with a decent treatment plan, so I don’t feel like vomiting round the clock, and maybe my legs will start working again, etc. Please think good thoughts for me tomorrow starting at 3:30 PM.
I’ve been asked how I’m doing, so I’ll be frank – everything still sort of sucks, as you might imagine as I’m only on symptom control as of today, and really it’s been hard not being able to speak easily, swallow pills easily, remember things, dropping stuff, and oh yeah, remembering I might throw up or fall at random times and staying on some absolute knock out pills for the nausea and dizziness round the clock. I haven’t been able to put on any weight yet. I don’t really feel better yet. I’m hoping that’ll change as of tomorrow.
I did start being able to read in teeny doses – otherwise I’ve been on a steady diet of TCM and HGTV to entertain myself, while everything else does weird stuff to my eyes to make me dizzy. It’s hard to type, (SO CLUMSY!) but here I wanted to show up for a quick update while I was up for it.
I’m also going to beg my Science Fiction Poetry Association Friends to please vote for Field Guide to the End of the World for the Elgin Awards – votes are due for members September 15! Here’s the link: https://docs.google.com/forms/d/e/1FAIpQLScC4YJ4eDbRAXqpEMPcEpIsrqPl19k_fjQtFG_J7-c5OZj2ZA/viewform?c=0&w=1
There are a lot of great books and chapbooks up this year, including many by friends like Nancy Hightower, Margaret Rhee, Jessie Carty! And I think we could all use a pick me up. It’s been a rough year for a lot of us.
I hope to have some good (or at least better news) next time I post. In the meantime, send me your positive vibes! I hope fall gets here soon for all of us. (And of course, prayers for my Texas friends!)
Some Time in the Hospital, a New Diagnosis, and a Tor.com shout for Field Guide to the End of the World
- At August 15, 2017
- By Jeannine Gailey
- In Blog
10
First of all, thanks to Abby Murray and Lish McBride for writing up Field Guide to the End of the World for this feature on Tor.com! This was a bright spot in an otherwise challenging week
I spent the last three days admitted into a hospital – after a week of repeated trips to the ER, collapsing with dehydration and fainting and cyclical vomiting – hooked up to IVs, getting lots of MRIs (three!) and giving lots of blood. Before that, I’ve had over a month of very strange symptoms – dizziness, nausea, vomiting, inability to keep down food, and strange heavy feeling in my lower legs, with wobbliness and my knees giving out. At the hospital I had a neurologist specialist work me up along with the hospitalist (along with, among others, a nutritionist, an occupational therapist, and a physical therapist.) It should be said here vomiting is one of my most hated things in life and the other is being hooked up to a damn IV. Even at a very nice hospital with private rooms and big televisions and pretty surroundings, like Swedish Issaquah, no one loves being in the hospital.
Several different radiologists and neurologists have decided my symptoms, combined with a rather devastating new MRI of my brain, mean I have probable MS. This has qualified me to be worked up at the best MS Center in Seattle with one of their top doctors. (If these doctors hadn’t interceded for me, there’s almost no way I would have made it in with their doc within two weeks notice.)
A Year After I Received a Terminal Cancer Diagnosis, I’ve Received a Positive MS Diagnosis.
A year and a half after I received a terminal cancer diagnosis at an ER in Redmond, I’ve discovered that my neural lesions, which had been watched for over five years and stayed pretty static, had changed, grown, spread, and generally developed a pattern that looked a lot to the neurologist and radiologist like MS. (The medical terminology is “McDonald’s criteria.”) Because I cannot have a spinal tap – the usual way to get a diagnosis – my diagnosis has been slow to come, even as I developed more lesions and more symptoms. This latest weirdness has been termed an official “MS flare,” which typically last thirty days and bring lots of symptoms on to the unwary MS sufferer.
MS is not as scary a diagnosis as terminal cancer, and MS is treatable – though we don’t know yet what kind of treatment will work for me. Currently I’m on a giant cocktail of meds to get me through the time when the MS specialists will decide what the best treatment for me is (because of my other health conditions, they didn’t want to do the usual throw a huge dose of steroids treatment at me. Though I might have welcomed it!) My brother came to visit me in the hospital, and my parents flew out to Ohio to help Glenn as right now I am termed a “fall risk” and can’t be left alone even if I wanted to be. Getting out of a chair or taking a shower have become huge difficult challenges for me all of a sudden.
Anyway, it’s been more than a month since I could focus on being a friend, a writer, or even a decent human being, so I apologize – – but just trying to survive the constant vomiting – along with a huge decrease in my ability to walk or even stand unaided – has been a real bear. I hope that the new cocktail of drugs will work until they can get me under a more stable treatment plan. Think good thoughts for me as I am dealing with a new reality. I said to a friend that MS wouldn’t even be the scariest thing – or the thing most likely to lead to be death – that I’ve been diagnosed with. But it is still a challenge as I learn the new reality of my body, which constantly morphs. Like Buffy, you learn to defend yourself against one monster one week, and the next week, another pops up and you start all over again,
BookRiot and Poets for People Who Don’t Like Poetry, plus ER trips and Smoke on the water
- At August 06, 2017
- By Jeannine Gailey
- In Blog
1
First, thanks to BookRiot and Carolina Ciucci for including me on this list of “Poetry for People who Don’t Like Poetry.” Very good company there! Share if you like the article.
Second, I’m sorry if I haven’t been on top of things – I’ve been sick – several trips to the hospital and different doctors kind of sick, where I can’t stop getting – well – no graphics here, but let’s just say I’m having trouble keeping down anything but liquids, and sometimes not even those. They can’t figure out what’s wrong though my white blood cell count is sky-high and other inflammatory factors, they’ve misdiagnosed me twice already and given me a bunch of meds that didn’t help, so I’m a little frustrated (and tired, and having a hard time staying hydrated or doing anything but sleep with all the anti-nausea drugs. Oof.) This has been a month so far, with no relief. Boo. I have things on hold – haven’t been writing and sending out as much, so forgive me if I have been slow to respond.
Also in the weird zone, the British Columbia fires – 500 miles from us – have covered Seattle and the whole state of Washington in smoke, and this along with a bizarre hot/dry streak have left us kind of living in an apocalypse zone, right when most of us would like to be spending time outdoors, the air is literally too unhealthy – not just for asthmatics, for everyone! Now everyone is wishing for rain and wind and lower temperatures. I can look over the valley from my deck, and a weird thick haze hangs over everything. The moon was weirdly orange last night, baleful even.

Sweeptpeas and lavender running wild in my garden
Here’s a quick clip of my garden in bloom. It doesn’t seem to be bothered either by the smoke or my illness, nor do the hummingbirds and stellar jays and flickers. We saw a coyote on our street the night we went to the hospital, and I saw this when I went out to water the garden yesterday – a tiny bunny eating the leaves off my dahlia! 


Jeannine Hall Gailey served as the second Poet Laureate of Redmond, Washington and the author of Becoming the Villainess, She Returns to the Floating World, Unexplained Fevers, The Robot Scientist’s Daughter, and winner of the Moon City Press Book Prize and SFPA’s Elgin Award, Field Guide to the End of the World. Her latest, Flare, Corona from BOA Editions, was a finalist for the Washington State Book Award. She’s also the author of PR for Poets, a Guidebook to Publicity and Marketing. Her work has been featured on NPR’s The Writer’s Almanac, Verse Daily and The Year’s Best Fantasy and Horror. Her poems have appeared in The American Poetry Review, Poetry, and JAMA.


