January 23, 2017
It’s 9 p.m., Friday, January 20, 2017. Yes, I haven’t written a blog about my new cat, his beauty and his “talking” to me as though he had some Siamese streak in him, my calling him Mr. Taksi, in part because of my taxi-driving father I loved. I’ve had the cat since January 3, although two days after he arrived, his eyes told me he was ill. At the same time, whatever is wrong with me, especially my ability to walk, has been growing worse so that I cried in rehab, not only because of the pain, but because it all felt so useless: walking three steps forward and metaphorically falling four steps backward. So what to do?
Victoria Pajak (Vicki), the woman who has been coming to my apartment at eight p.m. to give Mr. Taksi his evening eye drops and throat drops, knew nothing of my state of mind, but she chose one moment last night to tell me about her two cats, both of whom had been strays, and one of whom was totally blind. The two, normal and blind had been adopted together and they had grown up as close friends and delightful pets.
So, yes, I stopped feeling sorry for myself, at least for an evening. But it’s hard that I can’t pick up my cat—my arms are no longer strong enough to hold a 13-pound cat. Nor can I get down on the floor with him. And it will take some time for him to learn that he can have petting from me only when on the couch or the bed.
As for my own physical state, I’m trying to get an appointment with a couple of neurologists and hear their takes on neuropathy, if that’s what I’ve got (along with depression). I am trying to think about ways to be cheerful—and there’s politics to depress me daily, so that’s not the route to follow. Suggestions? I have used the usual: yes, I have my brain, and my fingers still work at the keyboard; I live in New York and there are taxis to get me to appointments; I still have a few old friends and I have made a few young new friends. I have a comfortable apartment. And I don’t have cancer or Alzheimer’s. So, Florence, I talk to myself: cheer up!
*Note: I’ve been typing journals usually every day, since returning from Mississippi’s Freedom Schools in August, 1964 and 1965. And long before computers, I typed journals on a typewriter. When I travelled, I wrote in tiny notebooks (and I have more than 100 of them). Later, of course I had a laptop when I traveled. These journals were both private as well as political. I would not have thought of sending them out to the world. But that’s where a blog has to go, and I was urged by Feminist Press to start a blog after my memoir appeared. It was hard not to confuse the blog with the journal, but I worked that out. I’m writing this today because this is the first of what I can call a blog/journal. It’s more personal than usual, or at least that’s how it seems to me. It’s also being filed with the journals, not the blogs.
December 19, 2016
For at least two decades I have been writing an end-of-year letter and sending it out via e-mail to friends around the world, including especially the African friends who worked on our four huge Feminist Press anthologies, Women Writing Africa
. I am also going to post the letter this year on my website (www.florencehowe.com).
Let me say, first, that I had hoped this letter would celebrate Hillary Clinton’s victory as feminist, humanist, and an experienced internationalist. Some of you who will read this were present in the Chinese auditorium two decades ago, as I was, when Hillary spoke that famous sentence: “Women’s rights are human rights; and human rights are women’s rights.” So our work will have to continue, and I am certain that Hillary will be on the front lines of that work.
My personal news is mixed. I continue to miss my active life of walking and swimming, not to mention travelling. Despite a dozen doctors I have seen, there is no real diagnosis, but only placebos, some of which have back-fired and been therefore abandoned. Right now I am counting on rehab and a clever, hands-on therapist to strengthen my right leg so that I might be able to walk with only a cane again. But I want distant friends to know that I remain in my own apartment, and I have made various adjustments so that I can be independent.
I write a journal every day which goes into a folder. And once a week or at least three times a month I write a blog which is posted on my website that I continue to maintain, with the help of Jen Petras, my dear Ohio friend. Writing keeps me sane, I think, and it is, as for many people, one way to work out their depression. I’ve also been writing poems, some of which I may decide to post on the blog as well.
What else do I do (aside from seeing doctors)? I go to the opera and to theatre, usually with Helene Goldfarb, occasionally also with friends Shirley Mow, Elyse Hilton, Don Thomas, Jorge Cao. Elyse also visits to talk literature and to help me walk when the weather permits. AnnJ looks after my needs in certain magical ways, and she visits frequently, given that she lives in Washington, D.C.
The most striking family news is that granddaughter Dr. Florence Wright, named after me, moved to Los Angeles almost a year ago and was married last week to Jason Neville, a Louisiana-bred city planner who works for the mayor. Other family members continue to thrive in Kansas, Mississippi, D.C., and even Brooklyn, though except for AnnJ, I see them rarely.
What do I do aside from entertainment? I sit on four Boards, though I am not as active as I used to be. I still long for real work, though I am also a realist about its disappearance from my life. Occasionally, I have proofread or copyedited for the Feminist Press. I am very proud of the fact that six books published by the Press have had favorable reviews in the New York Times
Finally, perhaps you are wondering how I manage being alone at 87. What do I do that gives me pleasure? Sometimes great pleasure? It’s reading and writing, of course. A good movie sometimes—I saw Rainman
last night here in my study. A good play—Heidigger
, which I’ve seen twice, was excellent, as was Master Harold and the Boys.
As for books, the list would be too long for this letter. I continue to be a fan of Kazuo Ishiguro, have read all his books.
And yes, there is the writing. Why don’t I get on with it? Why do I write only journals and blogs? It’s like asking the question about the election: why were so many people taken in by a fast-talking, know-nothing egomaniac (and these are kind words for the man)? There are many answers to these questions, mostly not heroic but mundane. The best I can do today is to say what my favorite diva sings, “I’m still here.”
Finally, I want to dedicate this blog to the little dog who kept me company when Don and Jorge travelled. Yoya died at ten of heart disease. The happiest, sweetest bundle of fur just keeled over upstairs, after a walk. She has been replaced—yes, it’s possible with pooches—by Fefa, hardly six months old. I know you will like the photos of Yoya.
August 1, 2016
Midsummer has come around quickly, and I’m still optimistic, though I have not had another diagnosis beyond A-Fib, and though I now own two “walkers”—machines on which I can lean as I walk. One of them, a three-wheeler with a bag for some carrying, Elyse Hilton found on Amazon, and set up for me when it arrived. The other was a surprise from my darling and intrepid daughter-in-law, AnnJ, who found a small, two-wheel walker that folds into a small unit that could fit beneath a theater seat. I was set to surprise her with the three-wheeler, but she really knocked me over with the one she had shipped to cousin Lori here in New York to present to me.
My friends know that I’ve been staunchly opposed to moving beyond the cane, seeing walkers as a negative signal one step from a wheelchair. But I was wrong, and now I know it. It was all probably vanity. I want my health (and even my youth)—who doesn’t? And I must learn to deal with reality. Aging is tough, on bodies and minds. It’s not for the faint of heart; it’s not for those who prefer living in delusions.
So, yes, I am grateful for work that interests me: for the volume to be called What I Left Out, I’m making progress on the difficult essay about my brother who committed suicide in 1985, and about whom I had little to say in my memoir. It’s always been difficult even to talk about him, and it’s one of the areas of my life I can honesty claim not to “know” or “understand.” I say that also about a number of things in my life. But of all of them, this is an old and life-long puzzle—and perhaps you have one in your life: How could two children, brother and sister, three years apart, be so different, never become friends, never share any of life’s views or values? I’ve assumed for years—yes, I’ve been trying to write about this for years—that I was probably guilty for not doing something to change the way we grew up and became adults. Hubris? Probably. Not for the first time in my writing life, I am discovering that writing helps to unlock mysteries in one’s own life. I’m discovering once more that writing stirs my memory. August 1 was my brother’s birthday. He would have been 85. He killed himself in 1985, when he was 53.
July 1, 2016
I was shocked to realize that I had not written a blog in more than a month. Do I have an excuse? Do I understand why this has happened? My last blog is up: on my dear friend and author Louise Meriwether, who is at work on a film script for her novel, Daddy Was a Numbers Runner
, a possibility that came out of the Feminist Press event I wrote about in May, in my last blog. At this end of this blog, I will describe the newest event in Louise’s life. And keep in mind that she is almost ten years older than I.
What I’ve been doing this past month is, once more, attempting to get some medical clarity about why I can’t walk easily or normally. My general care doctor’s response to my being able to walk only very slowly was that that was sometimes an early symptom of Parkinson’s disease. Which made me think of seeing a neurologist, perhaps the very one who had helped Mariam Chamberlain. This man saw me immediately and recommended some tests, one of which indicated that my balance must be somewhat related to the lack of a functioning right ear. This doctor tried to help by prescribing medication which would assuage the balance in some chemical fashion. Good idea perhaps, but my system rejected the medication as causing still more imbalance and dizziness. Then we talked a bit about the fact that I was walking anyway, but only when accompanied by a strong person whose arm stabilized me. I then mentioned that because I was so out of shape, I had to stop frequently to catch my breath. The next thing I was directed to do was to see a cardiologist and I was given a name, a phone number and urged not to waste a moment before calling.
I followed instructions, made an appointment, and then thought about it. I felt silly because, within the last six months, I had had two or three examinations by my general practitioner and had asked him about my heart and had heard him pronounce my heart excellent. So why was I incurring more expense and spending more tax dollars? But then I thought about a recent walk with Don Thomas four or five short blocks to the AT&T computer store on 72nd Street. Yes, it was a hot day. But we had to stop every few steps, and in the middle we sat down on a bench I had spotted.
So I called again and requested the appointment on Tuesday of this week. And the examination was unlike anything I had ever experienced. Two different brief procedures, the first resulting in a page the doctor could hold in his hand when he came in to do a further test which appeared on a computer in the room as he moved his “wand” around my heart. The result: indeed something is “wrong,” though the doctor claimed it was not “terribly serious.” I have A-Fib for short. The atrial or top part of my heart doesn’t seem to be working, which has resulted in the bottom working harder than ever. At least that’s my way of thinking about it.
So, yes, I need more tests: I’m to go to the doctor’s office next Thursday to be strapped to a small machine for the following 24 hours, which will produce a printout that will describe how my heart copes with various things I might do in that time. Yes, will keep you posted.
Note promised about Louise Meriwether. The Feminist Press has announced a fiction contest in Louise’s name. See the website for detailed information about the rules and rewards. http://www.feministpress.org/news/fp-tayo-literary-announce-louise-meriwether-first-book-prize
"Everyone concerned about global feminism, women’s contributions, and humanity’s future will be enhanced and enchanted by A Life in Motion
.”—Blanche Wiesen Cook, author of Eleanor Roosevelt: Volume I and Volume II
Lecture delivered by Florence Howe on January 8, 2011, at the Modern Language Association Annual Convention
“It is impossible to imagine women’s studies without Florence Howe. Myths of Coeducation
shows her vision and courage, insight and dauntlessness.”–Catharine R. Stimpson, Rutgers University
A revised and expanded edition of the classic groundbreaking anthology of 20th-century American women's poetry, representing more than 100 poets from Amy Lowell to Anne Sexton to Rita Dove.
The Feminist Press at CUNY
The Feminist Press is an independent nonprofit literary publisher that promotes freedom of expression and social justice.
Modern Language Association
The Modern Language Association of America provides opportunities for its members to share their scholarly findings and teaching experiences with colleagues and to discuss trends in the academy.