Showing posts with label cartoons/drawings. Show all posts
Showing posts with label cartoons/drawings. Show all posts

Tuesday, August 16, 2011

Pride Goeth Before . . . Well . . . You Know . . .

Click to enlarge:


This was some weeks ago, and since I have become an expert on all oral-hygiene alternatives, thanks to suggestions from everybody.  The day after my appointment, I had to sleep for three hours after flossing — which was not encouraging.  But I think I was still exhausted from the outing, and I can report that I’ve been doing my duty since.  I have decided simple tools are best: a brush and twine.  And Larry reminds me that I do love the rubber poker-thingie for gum stimulation.  Highly recommended.


Sunday, July 24, 2011

Simplify


Lately I’ve been lying in bed thinking of things to get rid of.  I can’t recommend it enough.  Great way to let go of the person you were going to be but have turned out not to be.  Not to mention the person you were but are no more.  Also, the person you thought you ought to be, but never really wanted to be.

In the evening, when Larry is available to obey my commands, I use him to make my dreams reality.  Stacks of books to pass on and mounds of stuff for the thrift store are growing, as is the peacefulness and functionality of the room where I spend my days.

Bye-bye Priscilla the scholar, performer, painter, dancer, dresser-upper, crafter, collaborative theater facilitator, social conflict studier, biker, swimmer, hiker, traveler, etc., etc., etc.  Bye-bye Priscilla who turned sick in college and still wants to finish what she started then.  Bye-bye Priscilla who dropped out of graduate school sicker and thinks she’ll get back to those projects sometime, somehow.  Bye-bye all past Priscillas, who are just fine being in the past and don’t need to be dragged along forever.

Bye-bye Priscilla who wants to impress and Priscilla who must prove herself.  Bye-bye Priscilla who thinks, without admitting it, that owning cool interesting nice objects will make her somebody that matters.  Bye-bye Priscilla who owns for the “ought” inside, for the person who gave her the thing she doesn’t need or really even want anymore, except to be for somebody else, some little bit, something she is not.  Who has energy for that anymore?  Good-bye Priscilla who wants to be everything, do everything, please everybody, who thinks if she works hard enough, she will do it.  Good bye all.

Hello now.

Hello open space, possibility, stillness, listening.  My life is small, real, good.  My little bowl of porridge is not too hot and not too cold.  I have three good chairs.  I have places to lie down where I need them, and my bed is not too hard or too soft.  There’s Larry working on his computer upstairs, despite the heat.  There’s the lush world outside my windows and birds still singing about summer.  There’s death coming and life renewing.  New writing and art and friendship and quiet and truth calling.  And enough space opening, here in my room, my home, my mind, my heart, for what is to breathe uncrowded and become what will be.  My enthusiasm bubbles up, apparently eternal.




Wednesday, July 13, 2011

The Way It Is

Tuesday, June 28, 2011

Six Weeks Since I Posted

Nine weeks ago, my friend Alan went to the doctor for the second time with symptoms of numbness in the left side of his body and a dropped foot.  The doctor, who had previously said he wasn’t worried, now sent him to the hospital for an MRI.  Alan has been there ever since.

The images showed a mass in his brain, and a few days later biopsy confirmed it to be a malignant tumor.  The biopsy also caused bleeding in the brain, resulting in paralysis of his left side and a variety of other effects, some of them rather strange.  For his three weeks in the ICU, I didn’t know if I would ever have a real conversation with him again, and I knew I couldn’t go see him.  He lives far away.  This is one of the frightful things about being sick I hadn’t experienced yet: not being able to be with somebody you love who’s sick.



In place of traveling I sent him audio recordings of myself almost every day.  Then he was released from the ICU and took up the phone again—a kind of resurrection experience for me.  We’ve talked most days in the six weeks since.  These two months have been a complicated, hard, draining, beautiful.  



I feel content with what has been possible for me, honored to have been intimately involved, and a little trepidatious about what I can manage longer-term. Alan will be released from the hospital this week after having had six weeks of radiation, chemotherapy, and acute rehab.  The rehab continues; otherwise, none of us really knows quite what is next.  I’m hoping now to resume posting regularly here.



Here’s a poem by Alan, from I about a year and a half ago:

   That days like fall leaves
   fall, yet do not accumulate--

   arithmetic fail--
   nor yield decrease--

   their number at all
   can only then

   be one and one
   and one and one.

For more of his poetry you can go to http://magnoliapresscollective.com/Emily.html.

Monday, May 9, 2011

ME/CFS Community to President Obama: Help!

When Courtney Miller asked President Obama about the abysmal state of funding for ME/CFS research, he said,  “Now, I will confess to you that, although I’ve heard of chronic fatigue syndrome, I don’t have expertise in it. But based on the story that you told me, what I promise I will do when I get back is I will have the National Institute of Health explain to me what they’re currently doing and start seeing if they can do more on this particular ailment. Okay?”  To see the exchange for yourself, fast-forward to 46:50 in the following video:




My latest activist cartoon is a followup to Courtney’s question.  It’s meant to be faxed by Billions and Billions of people, along with their own messages, to President Obama.  Click on the image to see it full-size, and head to this link at the ME/CFS Patient Alliance forum for instructions on downloading the file and faxing.  (You do not need a fax machine to participate!)



Please re-post the Obama cartoon on blogs, forums, and websites.  Give my name, link back to Heaven In My Foot, and—most importantly—link to the instructions for faxing it to Obama.

(Thanks to Lynn and Tina for their work on this! and to Lynn for the idea to do it!)

Sunday, May 1, 2011

Insight of the Day

Wednesday, April 27, 2011


Tuesday, April 19, 2011

Consider the Evidence

Sunday, April 10, 2011

Untitled

Sunday, March 27, 2011

Some Sentiments Have Broad Application




Nuclear reactors come to mind.  
Also chronic, politically embroiled diseases.

Monday, March 21, 2011

Conclusion After Reading Too Much of the News

Monday, March 7, 2011

On My Way? (First Publication)


I haven’t been posting much writing on Heaven in My Foot for some time (boo hoo), but I have a good excuse (yay!)—always a great comfort in this life of desires and demands.  I’ve been writing for print.  And guess what?  My first publication came in the mail last week and should now be available at more complete newsstands.  Titled “Wine for Those Who Faint,” the piece was about 6 years in the making and appears in the current issue of Image (issue 68).  It’s a personal narrative of intertwined illness and faith framed by reading Leviticus, the book of the Hebrew Bible which lays out ritual law for the priests of ancient Israel, including the instructions for animal sacrifice.  The narrative of my illness covers up to about 9 years ago. 

Image is a journal of literature, art, and faith—“Beauty will save the world” is their refrain.  I’ve been reading it for a couple of years and have learned from experience to expect something that astonishes me in every issue.  I favor the poetry, creative nonfiction, and publisher-and-editor Gregory Wolfe’s regular essays.  Before reading Image I thought contemporary religious poetry was limited to pietistic doggerel; I’ve been happily corrected.  Image also produces a biweekly free newsletter on the arts and faith and does a bunch of other wonderful things that you can learn about on their website.

As I love it so, I will send a free copy of Image (issue 68 with my essay) to the first two inquirers who want to become acquainted with this great journal.  Just send me an e-mail and we’ll take it from there.  It can also be purchased at some bookstores (if they carry Image), and on the Image website here.

I have two other essays that will be published, so I hear, in books this year.  Taken all together, these developments give me the unfamiliar feeling of being on my way.  Where to remains unknown.





Monday, February 28, 2011

Taxes



I'll be spotty on posting until I get them done.

Monday, February 14, 2011

Contemplation

Among the zillion things I miss from my healthier days is the rhythm of alternating activity and stillness, social engagement and solitude, work and rest.  I don’t long for stillness and quiet like I used to; I’ve had an awful lot of both in the last two decades.  But I miss that longing, if you can imagine what I mean, and the satisfying of it.  Paradoxically, I can be rather busy in my nonfunctionality: busy in my head, busy trying to do things, busy responding to the demands of my body.  None of it is the free action that I want, but it is a certain kind of preoccupation.  Sometimes I still manage, despite my hunger for more, to allow less.  And I'm always amazed by how happy it makes me. It’s good to just look out the window at trees and sky, to dream, to listen to music and to silence, and to rest my mind—which certainly gets weary.




Monday, February 7, 2011

People Assume

People often assume that winter must be hard on me.  They’re wrong.  I love it.  Thermometer-watching is very entertaining.  It’s cozy by the wood stove.  Cold nights under my thick down comforter are much better for sleep.  And winter makes beautiful, often-changing visions outside my windows.  Besides, everyone spends a lot of time inside in the winter, so the contrast between me and Them is softened just a bit.  There’s nothing winter brings that’s as hard on me as serious summer heat.  


Here’s a lovely list at Green Words Growing of good things about winter.




Monday, January 31, 2011

The Umph to Act: Getting Press Coverage for XMRV and ME/CFS

The ME/CFS activist community is working nobly on Many Fronts.  One of the numerous big needs is getting more and better press coverage, both for XMRV and ME/CFS.  I think part of that effort should be seeking the interest of individual journalists.  Larry and I are focusing on Amy Goodman, host of Democracy Now! because we know and love the show and because Amy gives substantial coverage to stories, particularly on social-justice issues.  With conventional news outlets, one often needs to have some THING you’re doing to get the interest of the journalists.  With Democracy Now!, I think our story itself has a real chance of being compelling.

Last Fall, Larry wrote a letter to Democracy Now! about XMRV and ME/CFS, and I followed up with this cartoon plus a page of contact resources.  I plan to keep updating Democracy Now! as things unfold.  Persistence is key.  I hope other people will also write to Democracy Now! and will identify other journalists whose beat fits our story.  Anybody care to join me, either pursuing Democracy Now! or another journalist/outlet?

Click image to enlarge.

Monday, January 24, 2011

Tuesday, January 18, 2011

Thank You Dr. Mangan

When I tell people I’ve been faxing cartoons to Francis Collins, Director of the NIH, they usually ask, “Have you gotten any reply?  How do you know they're getting through?”  And I say, “I just send them off, I don’t know if they're getting there!”  But, some weeks ago I got an e-mail reply to one of my cartoons —from Dr. Mangan, Chair of the Trans-NIH ME/CFS Research Working Group.  It was a substantive little email emphasizing that our concerns are not being ignored and that the Working Group is focusing on getting money to researchers outside NIH.  Good goal.  So, here’s my reply to Dr. Mangan.

But first, a few vocabulary terms and orientation points:  (1) The CFS-SEP is the Chronic Fatigue Syndrome Special Emphasis Panel, a group of researchers who review grant applications.  (2) The CFS-SEP has been for some years populated with individuals with no relevant experience—especially dentistry kind of folks.  You can read more about it here. (3) An FOA is a Funding Opportunity Announcement — an invitation to researchers to submit competitive proposals for federal funding.

Double click to see bigger . . .



Sunday, January 2, 2011

Happy New Year!

Sunday, December 5, 2010

I Want You to Know, Mr. Collins . . .

Here's my latest activist cartoon faxed to Francis Collins, director of the National Institutes of Health.  Click on image to enlarge.


 
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Cartoons at Heaven in My Foot are licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.