Showing posts with label children. Show all posts
Showing posts with label children. Show all posts

Wednesday, January 20, 2016

Boots and Kids

I think all parents and teachers can relate to this:
A kindergarten teacher was helping one of her students put his boots on. He had asked for help and she could see why. With her pulling and him pushing, the boots still didn’t want to go on.
When the second boot was on, she was nearly out of breath.
She almost whimpered when the little boy said, “Teacher, they’re on the wrong feet.”
She looked and sure enough, they were. It wasn’t any easier pulling the boots off than it was putting them on. She managed to keep her cool as they worked together to get the boots back on – this time on the right feet.
He then announced, “These aren’t my boots.”
She bit her tongue rather than scream, “Why didn’t you say so earlier?” like she wanted to. Once again she struggled to help him pull the ill-fitting boots off.
He then said, “They’re my brother’s boots. My Mom made me wear them.”
She didn’t know if she should laugh or cry. She mustered up the grace to wrestle the boots on his feet again. She said, Now, where are your gloves?”
He said, “I stuffed them in the toes of my boots…
From Dailyheadline.com

Wednesday, December 18, 2013

What Is Better Than Money? Merry Christmas!

We cannot put up a Christmas tree (real or artificial) because one of our cats, Intrepid, eats all kinds of plants and nearly died once from ingesting a lot of plastic branches. (Thanks to a concerned vet who rushed to our house, he is a wonderfully fine herbivore today.) We can, though, note Christmas in many other ways with decorations outdoors, Christmas cookery, finding fun gifts for colleagues, and shopping for the kids and the grandkids.

Ah, shopping for the kids! That is a relatively new and wonderfully pleasant experience. When they were growing up, we never had money for shopping for them. Medical expenses for Doah and Noelle always robbed us of that particular pleasure, and visiting them in the hospital -- Noelle was there Christmas day for a number of years in a row -- meant little time for shopping of any kind had we had any money to engage in that popular activity.

Nonetheless, we have many pleasant memories from Christmases past. For example, one year we had moved into a new place with a fireplace. Donnie had built a warm fire on a cold Virginia night, and we sat together, enjoying the evening while the kids were sleeping. Five-year-old Doah, however, woke up and crept downstairs. Seeing the fire, he began crying loudly.

"What's the matter, Doah?" we asked.

"Ho-ho burn butt!" he sobbed.

For the sake of Santa Claus's posterior, we put out the fire. Doah went off to bed quite happily, satisfied that he had finished his task of ensuring a safe entrance for the deliverer of gifts.

Then there was the year that we had no money at all. Christmas celebrations of the traditional variety were seriously out of the question, especially since we were moving at the end of December. The day after Christmas, as we were taking our first load of household goods to our new residence, we happened to drive past a Christmas tree lot and noticed that the lot had been abandoned. In the back of the lot was a lone, sickly-looking, leftover Christmas tree. Lizzie and Shane jumped out of the car and delightedly dragged it over to Donnie, who lashed it to the roof. Off we went, pleased with our acquisition, although we got strange stares from passing cars. We later decorated our puny little tree with our traditional ornaments, turning it into a festively proud fir. Homemade gifts in the form of food items were the theme of that year. We decorated the tree with cookies, fudge, and other favorite items of the kids that they removed and ate New Year's morning, the day we had decided would be "Christmas" that year.

Other examples of special Christmas events abound. I will share some of them:
(1) Our introduction to Christmas with kids came when Lizzie, our oldest and at barely two years old too young to know anything about Christmas yet -- or so we assumed -- stood in her pajamas at the window as dark settled around our apartment on Christmas eve and suddenly announced, "Santa Claus is coming tonight!" Oh, no! There were no plans for Santa to come that night! Donnie dashed to the car. It was nearly 9:00. The only store still open was a Five-and-Dime, and all Donnie could find in it were little socks for Lizzie's doll. It was enough to make her happy, and from that day we began the practice of one present per child for Christmas.

(2) We tried to make the one gift something very special, but we could never predict our children's strange requests. For example, Lizzie at the age of eight, a precocious fourth grader (she had skipped second grade), asked for a college textbook on genetics. Her interest came from attending the university Russian courses I taught on those days when she had no school and spending the hour in my intermediate Russian course solving problems passed along to her by one of my students who was majoring in genetics. (He also proudly dragged her to the honors program director, who invited her to attend some lecture-form university courses, where she promptly fell asleep. Nonetheless, the director offered to "enroll" her in the honors program as an aspiring college student, but doing so became too complicated. She had to wait another four years before taking her first college course for credit.) When Lizzie, who did become a genetics major for about three years before changing her major to cognitive neuroscience, received her Santa-delivered genetics textbook, she ecstatically raced from house to house in our small neighborhood to display her treasure, then returned home, plopped down beside me on the sofa, and mourned, "None of my friends like my gift! They think it's dumb."

"Well," I asked her, "What do you think? Are you happy with the book?"

"Yes. It's exactly what I wanted, and I really like all the problems at the end of the chapters."

"What did your friends get?"

"They got dolls. That's dumb!" I don't remember Lizzie ever playing with dolls other than the one that needed socks when she was little, a soft pink lamb that my grandmother gave her as a toddler and that she has to this day, and a monkey that my grandmother made for her out of a sock that she eventually wore out.

(3) One year, no one had been in the hospital all year, and we had money for Christmas! It was enough to buy bikes for Shane and Lizzie, pre-teen and teen at the time. Donnie and I were as excited as children to be able to get those bikes for our kids. (Noelle, who is paraplegic, and Doah, who is mentally retarded, never were able to ride a bike, but they got gifts that they had asked for.) That year, Shane and Lizzie had made no particular gift request, and we played a very cruel trick on them. We hung only the bike-lock keys on the tree and hid the bikes behind the house. The keys blended into the ornaments, and after the other gifts had been given out, Shane and Lizzie had nothing. In true Shane and Lizzie fashion, they looked around the tree one more time and said nothing.

"Did all the gifts get passed out?" I asked innocently.

"It seems so," said Lizzie. "Shane and I don't have anything, but that's okay. We don't really need anything. We didn't ask for anything this year."

"Really?" I asked. "Are you sure there is nothing else?" Donnie pulled one of the keys off the tree and handed it to them.

"Oh, oh, oh!" Shane exclaimed, "We have a bike!" Clearly, he assumed that Lizzie and he would be sharing.

"Go look out behind the house," Donnie suggested, and they took off running. We regretted not taking a camera with us when we saw the look on their faces when they caught sight of TWO bikes! They were extraordinarily understanding kids. They knew what it had taken for us to gather the money for two bikes, and they were grateful to us every time they rode them. That was a special Christmas. Donnie got a bike the following Christmas, and for years the three of them would ride together on Saturdays while I spent the day with Noelle and Doah.

The most special Christmas, though, was not one when we had money for gifts but one when we did not. It came two years after the bike Christmas. That year, multiple surgeries drained our coffers dry. Fortunately, we had an artificial Christmas tree with which a relative had gifted us a few years earlier, so we put up the tree and decorated it. Christmas eve ultimately came, and we knew we had nothing for the children. Donnie and I contemplated another year of cookies and fudge, but before Donnie got down to cooking (something he had to do alone -- I am such a bad cook, I would have wasted the ingredients in preparing inedible foodstuffs), one of us -- I don't remember which -- had a scathingly brilliant idea, to quote Hayley Mills' character in The Trouble with Angels. Donnie had by then begun working as a computer graphist, and we conceived of making coupons for each of the kids for one-on-one activities with Mom or Dad: a snack at McDonald's, a special lesson in one of our specialties, private walks, an activity that the child would choose, and so on. Each child received a book of twelve coupons that could be redeemed at will during the year. They loved them, and they used every one of those coupons! That year remains our favorite. In spite of our annually increasingly brighter financial status, no year matched that one for that year Christmas lasted not one day but twelve months.

The end
: As I was writing this post, nostalgia made me turn to Donnie and start reminiscing about that very special Christmas. We want to repeat it. So, we have just decided to give our children and grandkids coupons for future joint activities this year. As for the money we had set aside for gifts, we are now excitedly planning how to get rid of it and have scads of ideas about where to distribute it. I will add a PS later, once we have decided where it will go.

Oh, this year is going to be such a great Christmas!

Friday, November 1, 2013

Animals for Iraq (Stuffed, That Is)

I have only a few minutes before leaving for work but thought that some of you might like to participate in a fun and charitable project: sending stuffed toys to the kids of Iraq. More information can be found on the Change Becomes Change website. What I discovered there, I am copying here as is. Go there, though, for the links and other interesting information.

Here is the initial post:

Do you have a few stuffies, loveys or other gently loved soft animals that your children no longer enjoy? Need to make room for new things from the holidays or upcoming birthdays? We clean out our toys, clothes and items usually with the season's change, so guess what we're doing this week?

We're doing one thing different this season though. Our no-longer-beloved stuffed animals will be shared with the youngest victims of war in Iraq: the children. It's impossible for me to see the joy and comfort that special stuffed friends bring my own children and not want to give that opportunity to every child.

My friend Asha at Parent Hacks and Heather at Rookie Moms introduced me to Edmay Mayers, a member of the U. S. Army Corps of Engineers who is currently stationed in Iraq. She's bringing a little love and hope to children in the villages of Iraq who might not have either, in the form of stuffed animals. It's important work that she's doing and we're ready to help...you in?

So, clean out your closets, purses, cars and drawers (we know they like to hide) to find those gently loved stuffies to share.

Instructions from the Parent Hacks website are:

You can request a FREE mailing supply kit for sending items to military personnel. The kit includes boxes, tape, labels, and customs forms. This will allow you arrive at the post office ready to ship. Please note the the supplies are free, but you must still pay for postage.

Via the USPS website, here is how you can request this kit:

Call 1-800-610-8734 (Packing Supply)
Choose your language (1 for English, 2 for Spanish)
Choose option 1 (For Express Mail, Priority Mail, and Global Express)
When you reach an agent, request CAREKIT04.
The agent will get your address, and the kit should arrive in 7-10 days.

Thanks for the inspiration and introduction, Asha & Heather.

UPDATE: You're going to need the following APO Address for the post office when you request your kit.


Chaplain – Camp Warrior
FOB Warrior – Kirkuk
Toys for the Iraqi Children
APO AE 09359

Now let's go find some stuffed toys! What fun!

Saturday, October 19, 2013

From Grief-Stricken Mom to Real-Life Angel: The Case of Casa do Zezhino

After telling some bad tales about my travels abroad (see, for example, Muggable Me), it seems like it should be time and only fair to tell a remarkably good tale that I learned about during my days of providing consultation to state and private educational programs in Brazil. It is one I have been meaning to tell for a while, and I do at least have a button about it under "Ways to Help Others" over there on the right-hand side of this page: Casa do Zezinho (Little Joe's House).

The following description comes from the English-language site:

"On the outskirts of São Paulo, there is a poor and violent region so dangerous, it is known as the 'death triangle.' Thousands of families live here and don't have the resources to move elsewhere. Children have no access to leisure activities—there are no libraries, no theaters, no museums, no parks to enrich their free time. In fact, on average, three children die in this neighborhood every week by violent means or neglect.

In the middle of this terror is a safe haven called Casa do Zezinho. This daycare and after-school center is a sanctuary for children and teenagers who take part in their educational programs as well as the arts and culture programs they offer. The children are encouraged to explore creative hobbies and engage in cultural activities as well as participate in self-esteem and self-development programs.

Dagmar Garroux, the founder of Casa do Zezinho, and known as Tia Dag, describes it as, 'A house where we learn with children, and children learn with us, how to open the doors which are usually closed by poverty.' Casa do Zezinho provides a sheltered place for the children to play and learn. It is a place where children receive attention, affection, nutrition and education. It is a place where they can find hope.

Their programs include the graphic arts: mosaic, paper recycling art, woodworking, ceramics and silk screening—as well as the performing arts: theater, dance, musical instruments, and singing. Instead of dead end roads, the children are shown the way to make positive choices for their own future."

What the website does not tell you is Dagmar's personal tragedies. I felt an instant bond with Dagmar when I learned that she had had a child with spina bifida, like my Noelle. Unfortunately, unlike Noelle, who has reached the grand age of 33 and counting, Dagmar's daughter died at the age of six. The loss of her daughter prompted Dagmar to found Casa do Zezinho. Instead of losing hope, Dagmar developed an approach to teaching (and life) that she called "hope pedagogy."

Beginning with just a few students, she had reached an enrollment of 300 when her father came to visit this marvelous oasis in the middle of Death Triangle. (I have been to Death Triangle and can personally attest to Dagmar's institution being a real oasis, where hope lives and grows.) Now, Death Triangle has earned its name: it has the highest per capital rate of murder anywhere in Brazil, and deaths come easily, quickly, and voluminously there. Dagmar's father was little more than one tiny number in a large statistic: he was murdered before he ever saw his daughter's triumph. She was heartbroken and angry and stayed away from Casa do Zezinho for a month after her father's death. Then, a group of older students came to her, told her that they missed her and that they had determined who had killed her father. They promised to take revenge -- kill the killers -- if she would come back. As she told me, she realized that this kind of thinking was just the opposite of what she had been trying to teach the next generation, and so she told them that she would only come back if they forgave the killers (and that she would, too). Forgiveness was had all around, and Dagmar came back in full force to build the institution to 1200 children and growing.

Dagmar's Casa do Zezinho is one of many examples of God turning bad into good. Dagmar's losses became a major gain for hundreds of children with some of the worst potential futures in all of Brazil; instead of looking at a life on the street, selling drugs, these children have learned about selling other kinds of things, things that they make, as well as have traveled to Germany to participate in a bi-cultural choir, giving them a perspective on life that ranges far beyond the small triangle in which they were born.

Good from bad is such a common theme with God. How can we we feel sorry at all for ourselves or our kids when God has used their plights to create delights? Because of Doah's experiences, many children who would otherwise have died have lived and a class of autistic children was left far less autistic. (I guess I should blog about the stories behind that statement some day.) Noelle has been a spokesperson for all kinds of disability-related events and campaigns, including being quoted at one point in the Washington Post for her testimony at a Congressman's hearing on special education (the only child to testify). Shura bonded an entire community that had only one desire: that he live (and he did).

And then there are those muggings where in just a few minutes I learned more about cultural aspects of the countries where I was mugged than I could ever have learned (or understood) from university studies. And, of course, there is the story of St. Francis Retreat; the new super-duper digs would never have been undertaken had not the old burned to the ground. Nor is it likely there would have been such a rallying of community support that is likely to last long after the new building opens.

I could go on and on about how many times and ways I have seen God turn bad into good, but I won't. I'll save the discussion for a future post when others can share their experiences, too.

I am, however, reminded every hour of every day of the goodness of God that is poured out upon the children living in a violent neighborhood in the bowels of Brazil through a real-life angel called Dagmar. You see, the clock in my office has the Casa do Zezinho logo, hand-drawn and given to me by a child from Dagmar's oasis.

Friday, October 11, 2013

Shura's Miracles

Next on the list of my children who have benefitted from the kindness of angels in the garb of professionals is Shura. (I don't know whether to include him among our children or not since he was with us for such a short while, but in the broader meaning of the word, he is our child even though Donnie could not even communicate with him in the beginning, Shura speaking no English and Donnie speaking no Russian.) Anyone who has read my book, Blest Atheist, knows the story of Shura in grand and glorious detail. I include it here in very brief form for everyone else and as part of the series of the positive things that other people have done for my children.

About Shura:
Shura was a dying child artist from Akademgorodok, Siberia, a place where I had done research, consulting, and teaching, and my second most favorite place in the world, the first being the little mission town I live in right now. (The picture on the left was drawn by Shura following his first surgery in the United States.) He was remarkably talented. As a very young teenager he had had two exhibits at Dom uchenykh (House of Scientists, which recognizes the leading academicians and artists in Russia, at that time the Soviet Union), poetry published in a collective volume, and a television documentary on his life. Shura was unusual in Siberia in that he was alive. Born with spina bifida during the Soviet era in a region with a paucity of antibiotics and no experience with these kinds of neurologic defects, accompanied by extremely harsh winters with temperatures dipping lower than 75 degrees below zero, and into a family of seven children (nearly unheard of in the USSR - the family required two side-by-side apartments in order to accommodate all its members), Shura grew up homeschooled by necessity in a country where such a thing was not only unheard of but also rejected out of hand. To make a long story somewhat shorter, through actions taken by Shura's godmother and me, Shura ended up in the USA for life-saving surgery. Here I was his guardian, and then he moved in with Julie Trudell (see Shura's caregivers below), and then began to live independently in Charlottesvile, Virginia as a chef and artist. While recuperating from his surgeries as a teenager, he was granted a residency at the Virginia Center for Creative Arts, the youngest person ever so honored. Last January he returned to be with his Russian family, now living in Moscow in the new Russia where antibiotics are more readily available and where Shura hopes to devote full time efforts to his art.

Shura's challenges:
Shura was born with lipomyelomeningeocele, a form of spina bifida, resulting in mild paraplegia (limited to no movement below the knee). He ambulated with crutches and, when allowed, on his knees. Over time, as result of untreated ulcerations that are typically for enervated skin, he developed gangrene in both legs, requiring an amputation of both. Ambulation is now accomplished with prostheses. Although he has a neurogenic bladder, he has refused to self-catheterize. Doctors were able to improve on his bladder functioning sufficiently to allow Shura close to normal bladder control. The lipomyeloneningeocele was not repaired at birth, as is usual in the USA, and until this day remains, now by choice, unrepaired; it has so far created no health damage. Concerns are that repair would result in hydrocephalus, which Shura does not currently have.

Shura's special caregivers:

Shura's family: These were the caregivers who kept Shura alive against all odds and then, when there was no longer any hope of keeping him alive in Siberia, handed him over to a stranger (me), fully trusting God to watch over him. (That faith was surely not in vain!) Shura's mother was a teacher, and she taught Shura at home; he is highly educated in spite of never having attended a regular school. She was also the faith center of the family. She knew that Shura was God's special child, and she made sure that Shura knew: he came to me full of faith. Shura's father, wounded in the war, walked with an energetic limp. A dreamer and printing press owner, he worked tirelessly on behalf of getting his son to the USA, gathering in money from visitors to Akademgorodok world-wide. When he delivered Shura to me, he handed me a large bag of coins and bills from many different countries, not enough to pay for anything of a medical nature but enough to help with clothing and feeding Shura. (Turning that sack of foreign money into dollars took an entire afternoon at Salts Bank, where foreign meant only Mexican -- everything had to be looked up in a book to ensure that the money was real.) A third member of Shura's family was his godmother, who had come to know me when I was lecturing in Krasnoyarsk. Ironically, she herself later developed cancer, and the doctors at the University of Virginia Hospital stepped in to take care of her, too.

Dr. Ronald Uscinski. Yes, the same doctor who played a vital role in the health and well-being of Noelle. Ron read Shura's x-rays and medical records originally and gave me guidance in how to proceed and what was needed medically. He then tirelessly filled out all the paperwork that the US Embassy in Moscow required to bring Shura to the USA three times. It seems that the embassy kept losing it. I had some doubts as to why the paperwork was getting lost, and the final time I noted that a copy of the fax was being sent to a resident of Moscow who could bring hard copy if needed. That took care of that. Hard copy was not needed. After examining Shura himself, Ron also stood by me and Shura when we made the decision not to repair the lipomyelomeningeocele for fear of causing greater damage, considering that Shura had already stabilized with the sac in place.

Julie Trudell. I first "met" Julie when she called me from UVA Hospital to tell me that she had tickets for Shura and me to come to UVA for Shura's surgery and a $500K for his care, all compliments of John Kluge. A mother of a son Shura's age, after our attempt at post-surgical follow-up from California (flying to appointments, instead of driving), she offered to take Shura into her house. Instantly, we had a triumvirate of motherhood: Siberian mother, Californian mother, Virginian mother. Early on, there was transcontinental, transatlantic communication among the three of us. Over time, Julie took on most of the late-teenage parenting. She and I have become like sisters over the past 15 years since that first phone call.

Dr. Vladimir Kryzhanovski. Vladimir simply appeared on the radar one day, telling us he had heard about a young Russian undergoing surgery at UVA. Vladimir was a cardiac surgeon on some type of exchange program at UVA Hospital, and he wanted to help. He was a ready interpreter in the beginning when Shura could not speak English. He inserted himself into the medical decision-making, e.g., insisting that the best kinds of prostheses, not the simplest (considered easier to maintain in Siberia), be made just in case Shura remained in the USA for a while (which he did -- 15 years). He spent hours talking to Shura about Russian and Ukrainian literature and other cultural phenomena, making sure that Shura never forgot his own culture (something he could do far better than I). Later, he helped Julie with parenting issues. (Oh, yes, Vladimir is still in Virginia.) My most vivid memory of Vladimir is the poignant picture of him walking beside Shura's gurney on the way to Shura's first surgery (the double amputation). I had to stop at the point that all parents have to say good-bye to their children, but Vladimir did not. He walked the rest of the way to the operating room with Shura.

John Kluge. Most of John Kluge's contribution is described above. I never met him. Shura never met him. He is now 94 years old and, the last we heard, suffering from cancer. I doubt that we will ever meet him, but Shura did paint a picture just for him. To give and not expect anything in return is true giving. The only requirement that John Kluge made of Shura was that the medical care was to be given at UVA and Shura followed by the Kluge Rehabilitation Center. You see, Mr. Kluge had given money to the hospital before and quite a bit of it. Mr. Kluge not only paid for the medical expenses, he also asked Dr. Gillenwater, who had just retired from the urology staff, to return for one purpose: to coordinate Shura's care. And then, to make sure that Shura was fully taken care of as time went on, he provided periodic money for clothes and painting supplies.


Shura's life has been full of miracles. The first was that he survived. A tethered cord, highly painful and if untreated highly damaging, typically accompanies a lipomyelomeningeocele. That was the second miracle; he has never had a tethered cord. The third miracle occurred when I happened to meet Shura's godmother in Krasnoyarsk and together set into place the series of events that would bring Shura to the USA at a time when the US Embassy was opposed to granting such visas. The fourth miracle was finding John Kluge as benefactor for we had no idea where to get the $50K upfront money that hospitals were requiring, let alone the $500K estimated total medical expenses (actual expenses have been nearly double that). Finding John Kluge was not easy: I had an address given to me my someone quite by chance from Charlottesville, Virginia, home of John Kluge -- except that was not his home; he lived in NYC. Nonetheless, the package and plea I sent to Charlottesville somehow found him in NYC within 72 hours of sending. The fifth miracle was the appearance of Vladimir in Shura's life -- who would have thought that there would be a visiting doctor from the Ukraine (in the former Soviet Union) just at a time when Shura needed translator, doctor-guide, and father figure in his life. The sixth and highly potent miracle was finding the overseer of the INS after a moleibin (Russian Orthodox prayer service) for Shura, a person who no longer attended that church, did not know about Shura's moleibin, and was 100% situated such that he could help with all visa and green card issues (and did); only later did we find out that this person was a convert who had been the recipient of a miracle himself (see Miracles in Real Life).

In the case of Shura, I often wondered, given all the miracles, anyway, why they did not happen faster. (Remember, I was still an atheist at the time, so I just considered it all serendipity, assuming that if there were a God, it would all have happened instantly.) Only now I understand. The journey was clearly more important than the destination. It was not the time for miracles that was needed. It was the time for people to see the miracles and to be part of them, the time to expand Shura's blessings beyond one young man to dozens of people worldwide.

Yes, indeed, Shura’s life has been full of miracles. Where there could have been great sadness, there has been great hope and joy. There has been only one stain on all of this: me. As an atheist at the time that all of this was taking place (Boy, could I make up excuses and shaky explanations for the series of miracles that rolled out before my very own eyes!), I set a poor role model for Shura, and I was, for him, a role model. As a result, he chose to abandon his faith for my atheism. There was logic, in both our minds at the time, for his choice. I was the one, in his mind, who had pulled him from Siberia and saved his life. He really did not understand that I was only the conduit that God chose and that God could have chosen another. Why would God send a strong believer to an atheist or allow that atheist to discourage the faith of His believer? That question, I suspect, will never be answered. I don’t really need an answer. I am just trying, somewhat unsuccessfully, to deal with the regret. (It is one of those situations where we know that God forgives us but we find it difficult to forgive ourselves – at least, that’s the way it works for me.) Shura knows of my conversion, and that has puzzled him. Perhaps there is hope for a reversion for him. (Please pray for that.) More important, now that Shura has returned to Russia, where care is at last sufficient for him, he will be living near his parents. I imagine that once again his real mother will take care of his faith.

Doah's Angels












Doah, helping Sue Scott with her large yard

Following the post on Noelle's Angels in Scrubs, this post tells the story of those who helped Doah. In Doah's case, both teachers and doctors were important, as was Andi Kush (but since Andi was introduced in the post on Noelle, I won't include her here except to say that her presence in Doah's life was as important as it was in Noelle's).

About Doah:
Doah is a 29-year-old young man, for whom doctors predicted only one possibility: demise before his first birthday. Some were very annoyed with me that I held onto hope that they considered unwarranted and naive. We survived a very shaky first 18 months as Doah's tracheotomy, the treatment for his subglottic stenosis, clogged again and again, resulting in 5 clinical deaths, two of which included heart attacks that preceded apnea. We all had to be very good at CPR because all of those deaths occurred outside of the hospital, one of them in my arms as I was nursing him. I learned all kinds of creative techniques beyond traditional CPR to get Doah breathing again, and his older sister became the youngest person (age 9) the local Red Cross ever trained in CPR. It was necessary. If Doah stopped breathing while I was in the bathroom, someone had to help him. As a result of our acquired skills, Doah survived all those cloggings. In fact, he was the only trached child followed by Renboro Hospital that year to survive the winter. As for me, I was a doctoral student and a teaching fellow. After his tracheotomy surgery I could not find an appropriate babysitter, and so Doah went to classes with me. Where I was a student, he sat in a baby seat beside me. When I was teaching, I placed him under the podium. One of my students, watching the difficulties, later became a social worker, committed to finding better solutions for parents of challenged children. Doah spent most of his school years in special education, where he managed to successfully demand that a class of autistic children interact with him (when we left, the school set about looking for another Doah -- an extreme extrovert in need of daily speech therapy to add to the autistic class for the following year in the hopes of repeating that success). During high school years, he singlehandedly convinced the gym teacher to integrate his special education class into regular education gym with his football player "buddies." At graduation, he received a standing ovation and was the only student, other than the valedictorian, mentioned by name in the town newspaper. He was also voted "class flirt," the first time in the history of the school that a special education student had won a popularity award. Today, Doah lives semi-independently in a group home in Santa Clara. He works in a sheltered workshop and has a free enterprise "franchise" there for selling chips and soda. With my help, he published a book of humor that has gained a following in Russia, where a professor of psychology at St. Petersburg State University translated it into Russian, in Moldova, where its short, simple, funny texts are ideal for use as tests in ESL classes, and, to a lesser extent in the USA, where he was invited to the 2003 national book exhibition in Los Angeles. (He was quite proud of his "author" badge.) On two weekends a month, he stays with us and can be found wandering around town, photographing whatever event is taking place; several of his photographs have been published.

Doah's challenges:
Doah was born two months prematurely, but he had no major problems directly traceable to that early birth because he was a big baby (4 lbs) and the doctor had given me steroids during my five days of labor, developing Doah's lungs and avoiding hyaline membrane disease, which was then the leading cause of death of premies of that gestation. Over time, we found one after another after another birth defect that had not showed up immediately at birth, for a total of 18 birth defects. Initially, Doah failed to thrive, which turned out to be attributable to his inability to digest formula, which the babysitter fed him. My body had adjusted to nursing at night only and so formula was needed during the day. The solution we found was a babysitter who could wet nurse him, and during a two-week period when I was called to active duty because of a national defense crisis, she kept him round the clock. She watched him until he had his tracheotomy surgery. The most serious of Doah's birth defects was subglottic stenosis, a narrowing of his trachea to the point that he could not breathe; for that, he needed a tracheotomy, which he himself removed without any of the medical staff noticing while he was at Cincinnati Children's Hospital, awaiting assessment for a crichoid split or laryngeotracheoplasty to take care of the stenosis. This was a premature take-down of the tracheotomy, so we had to keep our CPR skills current until Doah gained more airspace in his trachea through growth. The next thing discovered was a hiatal hernia; he still has that and the reflux that goes along with it. Then, a bifid uvula (just a curiosity) and a submucous cleft palate came to light. The decision was made by Georgetown University Hospital doctors not to fix the cleft palate because Doah's chance of survival was too low. Instead, we arranged for daily speech therapy; it has helped to some extent. After that, Doah needed surgery for an undescended testicle, as well as a bilateral myringotomy (ear tubes in both ears). Some of the other unfixable things discovered were malformed ears, a coloboma (failure of the eye to close in the back -- so rare that all of the eye doctors in training at Stanford University were paraded over to Lucille Packard Children's Hospital to look at it in case they ever saw another one), and extremely short stature. Over time and with testing, he was discovered to have ADD (some argued that he had ADHD, but Doah's hyperactivity was actually due to food allergies, specifically yeast). He also had 63 (!!) other kinds of allergies. When Doah reached the age of 12, Stanford University Hospital learned that some doctors were identifying a syndrome that Doah might fit: CHARGE Syndrome. The identification would not help Doah, however, because from what the Stanford doctors could determine Doah was the oldest survivor of the syndrome and therefore while his progress could inform doctors about what to expect with younger children, there was no way to predict what to expect with him. There were other, minor defects, some of them associated with CHARGE Syndrome, including a heart murmur, but the ones described above were the most troubling. Oh, and either congenitally or as a result of lack of oxygen from apnea and the tracheotomy, Doah ended up mentally retarded.

Doah's special caregivers:

Dr. Richard Paul was Doah's first pediatrician, and he was amazing -- a gift from God. He trusted us implicitly from his experience in working with our other children. If I said something was wrong, he reacted immediately because I usually handled run-of-the-mill illnesses without comment. He also trusted my decisions, the most dramatic of which was to steal Doah from Renboro Hospital and take him to Children's Hospital in Boston while the Renboro doctors were in court, trying to get custody in order to do a fundoplication that I was sure Doah would not survive and which was not a very successful kind of procedure, anyway. Since Dr. Paul twice supported me against the staff at Renboro Hospital (once when the doctors wanted me to stop nursing the baby for the convenience of the hospital staff and did not take into consideration Doah's failure to thrive on formula and once at a meeting that Dr. Paul himself requested with all the staff and me because he did not find the care coordinated or self-expanatory enough), I felt comfortable telling Dr. Paul about my plan to steal Doah. He said that while he could not condone my plan, if I were to carry it out, his partner's son was a resident at Boston Children's and could create a link back to the pediatrician. Armed with name and phone number, I went ahead and stole Doah in a rather dramatic scene, which had me fleeing down the stairs ahead of security personnel with Doah half-wrapped in a blanket, jumping into the idling car where Donnie was waiting for me on the curb outside the hospital in case we needed a quick getaway, and zipping off to the airport. We made it! And Boston Children's staff disagreed with Renboro's plans. Without an operation and with sensible nutritional care, Doah gained four pounds in one month and was discharged as a relatively healthy baby.

Dr. Colodny was the Boston Children's doctor who rescued Doah, stood up against the plans of Renboro Hospital, forewent an operation, prescribed a successful treatment, and, most important, listened to my experience of Doah and took that experience into account in prescribing treatment. I knew he would because he was the doctor who took down Noelle's colostomy (oh, yeah, I forgot to mention that she had had that in the previous post -- oops; too many medical issues to remember them all 30 years later) and who agreed with Dr. Moffett not to require Noelle to take prophylactic antibiotics (see "Angels in Scrubs"). Ironically, it turns out that he is a friend of Dr. Kennedy at Stanford who is Nikolina's attending physician.

Dr. Robin Cotton was the doctor at Cincinnati Children's Hospital who figured out the source of Doah's stenosis: aspiration of breast milk. Ironically, that which allowed him to thrive had caused the problem that was threatening his survival. More important, though, Dr. Cotton knew that Doah would outgrow the problem. At the time, it turns out that Dr. Cotton, who had recently immigrated from Canada, was the only doctor in the USA who knew anything about tracheal stenosis. Most important, when the Renboro doctors refused to give me a consult for a second opinion -- they were still mad about my stealing Doah and thwarting their custody attempt -- Dr. Cotton took Doah without any paperwork and somehow managed to get the insurance to cover the costs.

Dr. Doris Rapp is the author of the book, Allergies and the Hyperactive Child. Her book was our first indication that Doah's hyperactivity might be food-based. After seeing her on 20/20, I sent her Doah's records and asked what she thought. She called me at work. I was floored since she did not know me. She told me that Doah was too complicated for her but that Dr. Sydney Baker at Yale University could handle him. Unfortunately, Dr. Baker had retired. On the other hand, fortunately, Dr. Baker was a friend of hers. She had called him and asked him if he would come out of retirement to work with Doah -- and he had agreed! The kindness of strangers -- there are no words! Once again, I was floored.

Dr. Joan Landy was Doah's first teacher. She taught him to read when that seemed impossible. She taught him to sit still when that was clearly impossible; she asked our permission to use something that is no longer used: a trip-trap chair that encircled him, holding him still. She also named her very active puppy after him! A university professor prior to returning to teaching, she had taught the teacher of the autistic class that Doah subsequently attended when we moved to another district, and she helped that teacher understand Doah. She kept a daily journal between her and me so that any little thing could be taken care of as soon as it arose. Once, years later, when I called for advice, she told me that I would never guess what she was looking at as we spoke -- a picture of Doah that she had kept on her desk (she had become the head of special education) for a half-dozen years! When Doah graduated from high school, she had the announcement framed as a gift to him.

Sue Scott was Doah's last teacher. Although teachers in-between Joan and Sue had given up on improving Doah's reading skills, Sue did not and little by little, her efforts were met with success. If only she could have had him for more than his senior year! Doah's senior year differed considerably from other years. We had been forced to remove him from the Salts schools for fear that he would disappear (long story, not for this post). At the same time, I had been offered a one-year position at NASA in Houston. While I was trying to figure out where to send Doah to school -- in San Diego with Lizzie, his oldest sister, or in Houston with me -- my brother, Rollie, called and offered him a home there. So, Doah attended Hayes High School in Ohio. As the year ended, Rollie's apartment complex manager said that Doah could not stay after graduation because of rules against multiple adults in one household. So, a group home placement for post-graduation living and a sheltered workshop for learning to work had been arranged but was not quite ready on time. There would be an all-summer gap. The problem was widely known. Sue called me in Houston and offered to let Doah move in with her over the summer. I could not believe what I was hearing! I had come to know Sue well from my frequent trips to Ohio, and I trusted her completely. Such an offer, though, was almost unfathomable! Doah not only spent the summer with Sue, but once he and I had both returned to California, he spent a couple of work vacations with her. If he goes to Ohio to visit Uncle Rollie, he also goes to visit Sue!

So, once again, there is another side to the perhaps somewhat negative picture I painted on recent posts about Doah (see Doah, This Time and To Conserve or Not To Conserve). Clearly, some of the doctors made some very wrong judgments and as a result we almost lost both Doah and Noelle. Doah, especially, was difficult because he had a very rare set of anomalies, about which nothing was known in the 1970s. So, some of our frustration came from wanting and perhaps unreasonably expecting the doctors to know that which they did not and could not at the time know. But when it is your child, the expectations are high! What made everything manageable is that God sent us just enough brilliant, caring doctors to keep Doah alive and completely overwhelmed us with caring teachers and care providers who went so far beyond the pale to help us that the pale disappeared from view. There is no way we can ever repay these wonderful people. We can only pray for their long-term well-being and happiness and pass on to others the love that they, God's angels in professional garb, showed to us.

Thursday, July 2, 2009

All God's Children

My last post got me to thinking about God's children. I am referring not to mankind as God's children, but to the little ones in our lives and our second generation regardless of age, the ones who call us Mom and Dad (or Ma and Pa, or Omy and Baba, etc.).

In this, I cannot imagine anyone with a greater sense of humor than God. I see that humor unfold in my life time and again. For example, I never particularly wanted children; I had a career lined up for myself (in my mind). Well, had that career happened as planned, it would not have been one iota as interesting as the career that unrolled, in zigs and zags, before me. And had that career not had to zig and zag around child after child, I would have missed the richest moments of my life.

In a display of great irony, the children that came into my life were not your everyday variety. Well, actually, those, too, ended up in my life, but as adults. My birth children, as well as those who came to live with Donnie and me as children and teenagers, were different: highly gifted, mentally and physically challenged, medically needy, discarded, bereft, foreign. First came my own birth children, one after the other, in spite of my best efforts not to get pregnant. (I hated being pregnant -- if I had a half hour of not being sick throughout all four pregnancies, I do not recall it. As best as I can figure, between all the kids, I have spent 26,298 hours vomiting or trying not to vomit.) On the other hand, once the children were born, all those maternal instincts took over and ran way ahead of me.

After my birth children along came Shura (a Siberian teenager with spina bifida),

All of these children I have talked about in various posts and books. The ones I have not mentioned are the ones that came later. They are the ones who need my help (and your prayers) today. Please meet Lana, Ibrahim, and Maha.

Leyla and Shem (not related to each other) are from Iraq. I met them in Jordan, where they worked for me as work-study students at the university where I was the chief academic officer.

Leyla would periodically come into my office and say, "Mum, may I cry in here?" It was usually because she had heard of a new bombing along Airport Road in Baghdad, where her family lived, or an attack on Baghdad University, where her father taught. Her family could not leave Iraq. She could not return, and communications, especially in 2003-2006 were very poor and, at times, totally lacking. Given a tendency to assume the worst, when she did not hear that her family was okay, she assumed that something bad had happened. And so, she started calling me "Mum" and looking to me for advice and moral support. I took to keeping an Islamic prayer rug in my office for her use, as needed, as well as provided guidance and hugs, as needed. Leyla recently ran into legal problems with an expired passport and the inability to return to Iraq to take care of that issue. I was in Jordan earlier this month for business purposes and called Leyla, worried because she has not responded to email for several weeks. Someone else answered her phone, and if my understanding of the Arabic conversation we had was accurate, that phone number no longer belongs to Leyla. I worry about her. She is as much my child now as my own children. I know that God will watch over her and take care of her until I find her again, but nonetheless I would welcome prayers from readers on her behalf.

Shem was my student as well as work-study assistant. An Iraqi Christian (a small and persecuted group), he thrived in school in spite of being separated from his family, graduating with a 4.0. He has done well also in graduate studies and in subsequent jobs. He, too, called me "Mom," although it did not seem like he needed another mother. Still, he was alone in Jordan and lonely. He emails and Skypes me regularly, and his first words are always, "I miss you sooooo much!" Seeing him in Jordan two weeks ago reminded me how families are families, whether blood or not and whether separated by physical distance or not. We spent hours together. It did not matter what we talked about. I do not even remember half of what we said and did. Rather, I savored the blessing of being able to be together, if only for one day and one night, in spite of living half a world apart in cultures that are rather alien to each other.

Maha's situation is much different. She lives in Bahrain, and she became my "daughter" when I was consulting extensively (over a period of 5 years) for the Ministry of Education there. Shia Muslims, her biological family became embroiled in political machinations over a year ago when her brother was arrested in the dead of the night on a trumped-up charge that has yet to have its day in court. The situation is personally emotionally difficult for me--and truly not understandable--for Donnie taught and I was academic dean for many university students from the ruling Sunni Muslim Al-Khalifa family. The Shia-Sunni hatred dates back to the struggle after the death of the Prophet Mohammed and the murder of Ali, a tragedy and travesty remembered to this day on the 10-day annual Ashara (the word ashara means ten) when Shias take leave from work and commemorate this piece of history, in part by flailing themselves with branches to the point of drawing blood. One would think that this hatred would have died out after 16 centuries, but emotions still run high. Emotions are part and parcel of the Arab world. And so, Maha's brother has been imprisoned for 14 months, during which time he has been beaten to the point of being almost blind. I tried my best to help, and a friend of a friend convinced a specialist in international human rights to go to Bahrain, but to no avail. The US Embassy did not want to get involved, nor did any other international body, and the Bahraini government repelled any appeal. So, we wait--and pray.

I am sure that I am not alone in having adult children who are experiencing difficulties that require assistance beyond what a normal parent like me can provide. If you are one of those "mothers" or "fathers", what have you done? How has God helped you out with these children?