My name - Chava - means "mother of all living" in Hebrew. As a little girl, I
remember learning from my parents, both deeply religious Jews, that names are
very meaningful. Quoting the Jewish sages of long ago, they told me that parents
are granted a moment of prophecy when they choose their newborn's name.
I took their words to heart. Not surprisingly, children have always made me weak
in the knees. The fact that a 1955 bout with polio made me very weak in the
knees never deterred me from my dreams of motherhood.
People said that, given our disabilities, we'd be irresponsible if we went ahead and had a baby
At 15, I remember asking my doctors, "Will I be able to have children?" They
explained that polio had no effect on the reproductive system; getting pregnant,
they implied, would be no problem. "But, young lady," and here their voices grew
ominous, "your pelvis is deformed and your breathing is restricted. These
polio-related factors could jeopardize a pregnancy. And let's not forget your
arms; they're too weak to care for or carry a baby." One doctor found my
question amusing. "Aren't you putting the cart before the horse? First, see if
you can find a husband; then worry about having a baby!" His voice insinuated
that my chances for marriage were slim.
By the time I was 30, I was beginning to think he was right. My social life in
the Big Apple was active, but my dating life was nearly nonexistent. Then, in
1982, a miracle happened: I met a wonderful man named Michael Levy. We began
dating that December, during the Chanukah season.
What a glorious Chanukah that was! We were head over heels in love, learning how
many things we had in common: similar religious values, a passion for words and
music and, since Michael is blind, hands-on experience with disability. Married
in August, we prayed that G-d would grant us our deepest wish: to bring a child
into His world.
Cushioned by a euphoria common to newlyweds, we were amused when people - even
doctors! - asked us if we had consummated our marriage. Amusement turned into
annoyance when some people said that, given our disabilities, we'd be
irresponsible if we went ahead and had a baby. And in November 1984, when
doctors informed us that - due to infertility problems unrelated to our
disabilities - our chances of having a child were nearly nil, we were engulfed
by anguish.
That Chanukah, still stunned by the doctor's verdict, we hardly felt like
celebrating. Each night, as I lit the menorah and recited the blessing, "Blessed
are You, our Lord, who created miracles for our ancestors, in days gone by and
in our own time," I could barely hold back the tears. Would the miracle we
prayed for ever come our way?
Three months later, I was pregnant.
Our jubilation knew no bounds. The doctors groped for scientific explanations,
but as far as we were concerned, this was the miracle we had been hoping for. We
kept our thrilling secret to ourselves for the first three months and then,
bursting with joy, we broke our news to the world at large.
Perhaps we shouldn't have, because at the end of my third month, we lost our
baby. My obstetrician explained that I had a blighted ovum, a fertilized egg
that never developed. The hormones it produced made me look and feel pregnant,
but in fact there was no baby growing inside me after all.
This emotional rollercoaster ride sent us reeling. We struggled with painful
questions - Why did this happen to us? What did we do to deserve this agony? If
we were not meant to have children, why would G-d "tease" us with such
short-lived joy? - but the answers eluded us. We tried to keep our faith and
trust that G-d's love, although hidden, was still with us.
Then on February 26, 1986, nine months and four days after our miscarriage,
Michael and I learned that I was pregnant once again. Two days earlier, my
younger brother and his wife had their fifth child who, by higher mathematics,
was conceived just when our first conception faltered and failed. After months
of mourning and attempting to make sense of our loss, I felt that all was right
in the world once more. There was a G-d in the universe after all, and He had
decided that in our family tree, another life had to precede our little one's
arrival.
The doctor told me that once a woman has had an ectopic pregnancy, she is less likely to have a baby
My optimism swelled the next day when a man and his three-year-old son passed me
in the street and noticed me struggling to get myself and my motorized
wheelchair into a taxi. Without a moment's hesitation, the man brought his son
over to me, placed the boy's hand in mine, and told him, "Now, hold on to this
lady. I'll be right back." While he proceeded to put my wheelchair into the cab,
I marveled at the feel of this child's hand in mine, the look of his lovely
face, the sound of his barely audible voice when I asked his name. It was a
sign, I remember thinking as I looked at my deformed hand holding his perfect
one and noticed how he didn't pull away. This time the little one wouldn't leave
me.
A few hours later, I headed to my gynecologist's office for the official blood
test (a home pregnancy test had given us the glorious news). On the way, I
passed a little gift shop.
Attracted by a glass candlestick in the window, I decided to pop inside and
treat myself to it. I made my purchase and was about to leave when I noticed, on
the back wall, a display of children's puppet-washcloths shaped like various
animals. The variety was impressive - pigs, roosters, bulls, mice, frogs - but
the moment I spotted the pink and white lamb, I knew what my selection would be.
On our second date, my husband had shared with me a children's poem about a
lamb, and it had figured prominently in our courtship - as it still does in our
marriage. So I bought all the lambs in the store: one for my new niece, the
others for all the babies our friends were expecting, and one for our little
one.
The next day, I started staining. My euphoria turned to dread. Silently, I
begged our little one, "Please don't leave us. It's been only two days, but we
love you so much already."
It took several weeks to discover that I had an ectopic pregnancy: The embryo
was growing in my fallopian tube; if left unchecked, it could have killed me.
Ectopic pregnancies are usually terminated surgically. But because anesthesia
restricts my breathing, I spent a week undergoing a new drug treatment that
dissolved my life-threatening embryo. The doctor told me that once a woman has
had an ectopic pregnancy, she is less likely to have a baby.
It took several months to recover from our loss, but Michael and I soon were
back on the infertility circuit. Month after month came a slew of blood tests,
sonograms, hormone medications and doctor appointments. Month after month, my
supply of lamb washcloths dwindled as relatives and friends had babies; when
only one remained, I tucked it away next to Michael's love letters, suspecting
it would stay there forever. By the time Chanukah of 1988 rolled around, I was
overwhelmed by frustration and fatigue. I remember turning to Michael, the most
supportive husband in the world, and saying, "I've never been one to cut my
losses, but I can't keep banging my head against the wall. Do you think we could
look into adoption?"
That January, after consulting with an adoption attorney, we placed ads across
the country and waited by our new phone line, hoping to hear from a pregnant
woman in need of our help. The calls were few and fruitless. In mid-February, in
need of a break, we decided to spend a few days in Florida, visiting Michael's
parents. While there, I got my period. The usual disappointment turned to dread
when I noticed that the flow was barely a trickle, similar to my ectopic
symptoms. As we flew home, I said to Michael, "I don't care if New York is
battling a blizzard. First thing tomorrow, I'm going for a blood test. I can't
have this anxiety hanging over my head."
I can't carry Tehilah, but I can care for her
The next morning, I made my way across town to the lab where I'd gone so often.
All I wanted to hear was that I did not have an ectopic pregnancy, that this
strange period was perhaps a reaction to air travel. That afternoon, just as I
was about to light the Sabbath candles, the phone rang. "Congratulations, Mrs.
Levy. You're pregnant!" a cheery voice announced.
"That's impossible! I've got my period," I whispered. "And besides, we stopped
all fertility procedures and medications two months ago!"
"There's no doubt about it: You're definitely pregnant. Some women do get a
period during their first month; that's why they often miscalculate their due
date. As for your due date, it looks like it will be at the end of October."
Following that extraordinary phone call, Michael and I were too stunned to
speak. We sat together and, with tears in our eyes, prayed that this time the
Almighty would help us bring a child into His world.
He did. The pregnancy had its rough moments - a month of bedrest, a bad fall in
my eighth month, breathing and sleeping problems, a caesarian section - but G-d
did not abandon us. (Neither did our many friends and relatives whose prayers,
good deeds and optimism helped us through many months of anxiety and
anticipation.) On October 17, 1989, our breathtakingly beautiful daughter was
born. We named her Tehilah Sarah. Tehilah means many things: praise, a song, a
poem to G-d. And the Bible paints a poignant picture of Sarah (a name shared by
my two grandmothers), the matriarch who knew the heartbreak of childlessness but
lived to build a dynasty.
Today, as I watch our little one blossom, I remember my doctor's dire
prediction: "And let's not forget your arms; they're too weak to care for or
carry a baby." He was half-right: I can't carry Tehilah, but I can care for her.
When Michael is home, we can manage pretty well, each of us compensating for the
other's disability. Diapering Tehilah, for example, can be quite an adventure.
Michael lifts her onto the changing table, unfastens her diaper and holds her
legs while I wipe her and apply Desitin. If Tehilah is really dirty, we reach
for her lamb washcloth, hidden away for so many years. As she squeals with glee
and tries to grab it, joy overwhelms us.
Because Michael's job takes him away from us, we have hired a full-time
babysitter/housekeeper. She and I work as partners. At mealtime, she lifts
Tehilah into her high chair and brings me her food so that I can feed her. When
it's time for Tehilah's bottle, I lie down and Tehilah is placed on my stomach.
Our babysitter puts a small pillow under my wrist so that the bottle stays at
the proper angle. These tasks are tiring, but I wouldn't relinquish them for the
world.
We pray that Tehilah will teach them all that disability need not be an obstacle to successful parenthood
When Tehilah was seven months old, I actually discovered that I can carry my
little girl with the help of a baby carrier called Sara's Ride. We originally
purchased it with Michael in mind, figuring he could carry Tehilah on his hip
and still get around unencumbered with his cane. Well, as it turns out, Michael
rarely uses the device. I, on the other hand, have begun to carry Tehilah around
on my own! I sit in my motorized scooter and, once Tehilah is secured on my lap,
we roam the streets of New York unaccompanied! After an hour or so, fatigue sets
in - but how thrilling it is to feel so truly united with my daughter, with no
one hovering nearby to intervene. At day's end, we often head for Broadway and
wait for Michael to emerge from the subway station. When Tehilah spots her Abba
(Hebrew for Daddy) approaching, she gurgles excitedly. Michael stops in his
tracks and, when I verbally second her emotion, he beams with delight.
Passersby, notorious in New York for keeping their distance, smile at us as we
head for home.
People often ask us if Tehilah knows yet that her parents have disabilities. The
answer is yes - and no. When she was only seven months old, I discovered that
Tehilah's "pick-me-up" plea, indicated by arms stretched eagerly upward, is
never directed to me. And one evening, when she was eight months old, Tehilah
started whimpering while the three of us were watching a television game show.
We had no idea what was wrong. Suddenly, our unhappy little girl craned her neck
until she located me. She gave me a pleading look, turned back toward Michael
and then my way once more. "Michael," I said, "could it be that you're blocking
her view of the TV screen?" Michael moved slightly to his left and Tehilah was
content once more. More interesting than our daughter's fascination with game
shows is her awareness that visual obstacles are easier to resolve with her
mother's intervention.
So yes, Tehilah has learned that her parents have disabilities. But she has not
learned that, in the eyes of most people, her parents are "different" or even
"unfortunate." Seeing a wheelchair, a braille book, unfocused eyes or an
assymetrical body is commonplace for our little girl. And, speaking candidly,
Michael and I think that makes Tehilah a very fortunate person. As she gets
older, she will discover society's misconceptions about disability. But,
happily, children and adults who lack Tehilah's enlightened upbringing will
encounter a refreshingly bemused response from our little girl. We pray that
Tehilah will teach them all that disability need not be an obstacle to
successful parenthood.
As Michael and I anticipate Tehilah's second Chanukah, we remember the Chanukahs
that have come before. This year as I light the menorah for my husband and
daughter, I know my eyes will well up once again - this time with tears of
thanksgiving. Each night as I recite the blessing, "Blessed are You, our Lord,
who created miracles for our ancestors, in days gone by and in our own time," I
will thank G-d for our miracle baby. And each night I will add a special prayer:
May our little Tehilah grow up knowing that, as her name signifies, she is a
song, a poem to G-d.