July 13, 1964
This day holds a very special memory in my life..
Fifty-nine years ago, God had put some special people in my life.
This story actually begins back in November of 1956, when I had
my tonsils and adenoids removed, because they were very swollen,
making it difficult to breathe & eat. I was just about 2 ½ years old.
That was then. A few months later, I found myself making trips,
with my Mom, to the Speech & Hearing Clinic, which was on Park
Avenue here in Bridgeport, at the time. I wasn’t talking too much
yet, and when I did, it was hard for others to understand what I
was saying. They also found that I had a hearing deficit in my left
ear. It was not a good time in my life-to say the least. Little did I
know that it was about to get more difficult when I entered school.The visits to the S&H Clinic continued for three more years.
We lived in Trumbull at the time, and they did not have kindergarten.
I entered the first grade in September of 1960. I was still making
trips to the S&H Clinic, being excused early from school to attend
my sessions. I loved learning, but I didn’t like the kids who made
fun of me when I talked. It was very hard to understand why they
would do that, when I tried so hard to make friends with everyone.
At age 6, it’s hard to understand anything out of the ordinary. At
this point, I wondered whether the intense speech therapy was
really doing me any good. They really didn’t know what had caused
my speech impediment. They just chalked it up as a birth defect;
the same for the hearing deficit.
In the Spring of ‘62, on a glorious May 5th morning,
I received our Lord for the very first time, along with my cousin
Judy, at St. Teresa’s Parish! Little did I know that 19 years later,
I would be teaching religion to children with special needs,
at this same parish! During this time, some good news,
I would no longer have to go to the S&H clinic because the
Trumbull School System was offering speech therapy right
in the school!
A year later, I received a visitor at school. His name was
Mr. Kostopoulis, who was a Speech Pathologist. Of course,
I could not pronounce his name, so he told me to call him Mr. K.I had no idea who this man was, or why he came to visit me. I now
think of him as a special angel, because he led me to a doctor who
was able to help me. He asked if he could examine me. I looked at
Mr. Hofactor, the Principal, who had introduced Mr. K to me, and
he nodded that it was alright for me to go with Mr. K to the nurse’s
office. He then put a tongue depressor in my mouth, saying a lot of
“a ha’s.” After he was done, he told me that he knew of a doctor in
New Haven who was doing a procedure that he was sure could help
my speech impediment. He asked me if I would go to visit the
doctor. I told him he would have to talk to my parents, which he did.
I don’t remember exactly when we made the visit, but it was very
much like going to the S&H Clinic, with audiograms, and the taping
of my voice-lots of taping of my voice. This went on for almost a
year.
Speech therapy continued in school. I lost my Grandmother Maria
on my 9th birthday. I used to enjoy visiting her with my Dad who
would teach me to talk in Italian to her.. She had suffered a stroke
three years before, and was bedridden. She then came down with
pneumonia and passed away.
By this time, Beatle songs were playing on the radio, and my speech
therapist, Mrs. Watnick asked me if I liked their music. I told her
yes, I did, I sang their songs a lot. She said good, you can practice
your speech therapy while singing their songs!
Meanwhile, back at Dr. Howard Smith’s office, after having run
a battery of tests on me, found nothing new that we didn’t already
know-everything was a birth defect. My uvula was very short, making
sounds come out through the nose, instead of the mouth. All the
speech therapy in the world would not help, unless I had the
operation. Yes, I had to have a 5 ½ hour operation. What was he
going to do during that time? He was going to skin-graft the roof
of my mouth, and attach the skin to the uvula to make it longer!
This was not something I wanted to hear. This was a relatively new
procedure, so I did a lot of praying, because it was a bit scary, to
say the least.
It’s the Summer of ‘64, July 12th, my parents are driving me to
Grace New Haven Hospital, (now Yale) and Dionne Warwick is singing
“Walk on By.” on the radio. I wanted to “walk on out”, as we were
approaching the hospital. After all, the next morning, I would be
going under the knife, having the roof of my mouth skin-grafted. It
would make any one a little squeamish.
I didn’t get much sleep that night; all I could think about was the
operation. I had just turned 10 years old, just 17 days prior. I was
not going to be able to talk for a whole week.(Those of you who know
me, You could imagine how hard that was for me!) I had to write
everything down on a pad. (No computers or Iphones back then)
When I woke up, my arm was wrapped up tethered to a board, with
hoses hanging on it. I was being fed intravenously. They didn’t tell
me about that. I thought I broke my arm! My Aunt Florence & Aunt
Antoinette were there with my uncles. Mom & Dad were there, too.
My siblings I didn’t get to see for a week; they were staying with
Grandma Helen & Grandpa Nick.
Communicating was a pain, having to write everything I wanted to say
on the pad. I was given lots of ice cream, applesauce, jello, and any
other soft foods they could give me. I got to do some Arts & Crafts,
with the other kids who were in the same wing as I was. I remember
making a jewelry box out of a cigar box, spray painting it gold, and
decorating it with shell macaroni. It came out pretty nice. I had
quite a few visitors, which made the week go by fast. Going home was
great, but there was more intense speech therapy waiting for me to
do. My sister turned 9 on July 31st, so we celebrated that. My Aunt
Florence called to tell me she was going to have a picnic-party for me
at her house. She invited the whole family; even some of my Dad’s
cousins came!
Life went on as usual. Fifth grade was a bad year. I won’t go into the
details. I had to repeat the 5th grade, due to the mitigating circum-
stances that made this almost the worst year of my life. I survived
it though, with the help of God.
This story has a unique ending. I had always thought, in the back of
my mind, my impediments were not birth defects. I asked God to tell
me the truth when He thought I could handle it. He did just that.
Fast-forward to 2017, when I was having trouble swallowing. They
tried to do some esophageal tests, where I had to drink some very
thick stuff, which made me aspirate. So I failed that test. They
decided to do a 3-D ultrasound, which revealed some surprising
evidence which supported my theory that my impediments were not
birth defects, as I had been told by the doctors. The ultrasound
revealed that my left vocal cord and the nerve leading to my left ear
had both been severed. This led to the realization that the uvula,
too, was severed, when I was 2 ½ during the tonsillectomy & adenoid-
ectomy. Well, what do you know-it was a case of severe malpractice,
but too late to do anything about it. The fact is, God revealed the
truth to me when He thought I could handle it. After so many years
had gone by. So many hours of speech therapy. So many hearing
tests. So many days of wondering whether I would survive the
difficulties and struggles. I now know the truth. I felt as though a
big weight was lifted off my shoulders. God was with me all the time.
Every step of the way. Waiting . . . just waiting to tell me what He
had told me years before.” These were not birth defects. You were
born perfectly”. Thank you, Jesus, for being my best friend.
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