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Amy B. Scher
With a history of chronic illness, Amy B. Scher set out to
discover the foundation of healing. She is an energy therapy practitioner with
offices in Los Angeles and Monterey, California. She is a frequent contributor
to healthcare blogs and has presented to groups including the Department of
Psychiatry and Behavioral Sciences at Stanford University. Amy lives by the
self-created motto: “When life kicks your ass, kick back.” She is eternally
thankful for her years of illness and her ultimate self-healing.
About This is How I Save
My Life - A True Story of Embryonic Stem Cells, Indian Adventures, and Ultimate
Self-Healing
A fiery young woman with a debilitating and misdiagnosed
disease travels to a tiny clinic in India for a controversial embryonic stem
cell treatment. On the journey to save her miserably failing body, she finds a
world of cultural mayhem, radical medical treatment, and most importantly, a
piece of her life that she never even knew she was searching for.
This is How I Save My Life takes readers on a heartwarming
and often hilarious journey as Amy grasps at her last hope for health. Why do some
people heal from emotional or physical issues, while others don’t? Through
extensive research and her own recovery experience, Amy finds the most
important piece for her own healing—the impact of unprocessed negative emotions
on our physical bodies. This powerful and uplifting story of sheer
determination is for anyone who believes in—or doubts—the existence of miracles
and the infinite power of self-healing.
Connect with the
Author:
Book trailer: http://bit.ly/V8nxsl
Author website – http://amybscher-author.com/
Like Amy B. Scher on Facebook - https://www.facebook.com/amyscherauthor
An excerpt from This
is How I Save My Life: A True Story of Embryonic Stem Cells, Indian Adventures,
and Ultimate Self-Healing
By Amy B. Scher
I am lying face down in a hunter green gown (not a
flattering color for me) on a long, skinny table that feels like it was made
for a tall, slender man. Huge round lights that hang from the ceiling are
glowing on my body. A heater blows warmth in my face and three
operating-theater techs are by my side. Dr. Ashish comes in with scrubs and a
full mask covering most of his face. I can still see his smiling expressions
through it. He’s completely relaxed as always, but looks even more so since
he’s not in his usual fancy work attire. He asks me if I’m nervous and I return
his question with a genuinely calm, “Not at all.” They take my blood pressure
and see I am not lying. In fact, some people would be dizzy having blood
pressure that low.
Within minutes, it’s time for the procedure. My Old Navy
brightly colored fleece pajama pants under my gown are pulled down, mid-butt.
The table is tilted so my head and upper torso are tipped forward and it now
feels more like a balancing beam than a place to rest. I confirm with Dr.
Ashish that I won’t slide forward—and off. He laughs and reassures me. I wonder
if I’m the only one worried about this. The sister’s hand is on my butt and I
tell myself, if she had to, she could catch me by one cheek if I should slip.
Dr. Ashish feels intently for the right spot in my spine. He
injects a local anesthetic at my tailbone, at what feels like about an inch
from the tip. It hurts, but I know it will be over soon. A few minutes go by
and the anesthesia has set in. I soon start to feel an intense, deep ache and
awkward pulling. I accidentally wince and Dr. Ashish tells me he is pushing the
first syringe full of stem cells in. I can’t see his hand, but his arm is
steady like an iron rod. I breathe deeply, eyes closed while I try to inhale the
new life into me. I literally feel the stem cells being infused.
A heavy sensation quickly coats my lower back. If I knew
what it felt like to have an elephant sitting on me, this is what I think it
would be. I wiggle my toes to console myself. I know nothing is wrong but the
feeling is so strange that I want to check everything still works. A rising
sensation works its way up my spine as the second syringe of stem cells is
slowly injected. I imagine it like the red line in an old-fashioned thermometer
heating up rapidly. But it soon stabilizes and holds still in one place, about
halfway up my rib cage. I am giving Dr. Ashish a play-by-play of the
happenings. My right leg and foot start to tingle as the second syringe-full is
almost done being injected, and when it is, the needle is removed. When he
hears my left leg is not feeling the same, the table is tipped to the left; and
almost instantly I feel that side flood with equal sensations. I imagine my
spinal cord coated with stem cells, thick like glue.
Gauze is placed in the injection area and I lay still until
I am moved to a gurney and wheeled out of the operating theater. I am totally
and completely overwhelmed with emotion as I pass through the double doors that
lead to the elevator. I look up to see a Labor and Delivery sign and remember
how this hospital started off as a fertility clinic. I have flashes of this
same scene from when I had surgery to extract eggs from my ovaries during the
process of donating them to an infertile couple. I feel like I have come full
circle, and will never be the same as before I entered that room.
I am transported by a sheet from my gurney by two men and
placed face up on the bed in my room. The room is simply decorated (all white)
and nothing like my bright blue Green Park hospital room. Kids are playing on
the playground at the school next door. I hear them laughing louder than the
traffic chaos and can’t help but smile. The TV is small and far away from the
bed. I don’t bother turning it on. Bricks prop up the bottom of the bed, with
my head lowered toward the floor. This specific procedure was done to help
empower my lower body. However, some of the stem cells will travel upwards with
the help of gravity, which is the reason for this odd and oh-so-uncomfortable
position. I will have to stay like this for five hours. Within one hour, I have
to pee and my appetite is raging. Go figure.
Dr. Shroff comes to see me, and it’s so nice to have
company. She always has so many interesting things to say and I always have
enough questions to keep up. She brought me my two brain scan copies in
folders—the one from January and then the recent one. Reading the report out
loud, we get excited all over again about the progress. She leaves them on the
counter for me to take when I leave to go back to the Green Park hospital. Dr.
Ashish stops by to make sure I’m doing okay and after awhile, they are off to
see other patients.
The phone rings and I’m startled, but happy to have a
caller, even if it’s just going to be the reception telling me something
totally unimportant. It’s my dad (at a ridiculous hour in California) but they
want to make sure all is well. And aside from the fact that I’m starving and
banned from getting up to use the bathroom, everything is great. He begins to
congratulate me that the lesion in the left side of my brain is gone, but I cut
him off at the half-point in his sentence. “What?!” I say. “Yeah, I talked to
Dr. Shroff and she said it’s gone,” he replies confidently. I quickly correct
him. “Dad, it’s improved, but not gone.” He is sure Dr. Shroff used the word
“gone.” I reach up behind me without moving my spine and grab the folders. I
pull out the pictures from both sets and compare, holding them up in the air
above my head. I think I may have screamed. She was right—I can’t see one of
the lesions on the newer scan that was there on the first one, just one-month
prior.
When I get off the phone with my dad, I ask a hospital
attendant to have Dr. Shroff call me. She does within minutes and I tell her
what just happened. She chuckles and says, “Ohhh, so you looked at the scans,”
in her playful tone. Maybe it was supposed to be a surprise, although I have
become so detached from test results because I can intuitively and physically
tell I am better, that I’m not sure I would have ever looked. I tease her about
the cruelty in finding out such great news when I can’t get up and be excited.
We agree that soon I’ll do a dance and celebrate.
Five hours go by s-l-o-w-l-y, but then I am allowed to turn
on my side for an hour. When I turn (head still can’t be raised), I try to
funnel a very messy, saucy, Indian lunch into my mouth. I fail miserably with
half ending up between my lips and the bed. When it’s time to sit up, I’m
beyond grateful. If I’m not dizzy, I can go by car to “my” hospital soon. But
alas, I’m dizzy when I try. It takes some time for my head to get used to the
blood being distributed throughout the rest of my body because of the
horizontal position I’ve been in.
I’m back in Green Park after dark. My back aches and no
position I choose is comfortable. It takes me seemingly forever to fall asleep
as I have a serious case of the heebie jeebies. I know it’s a strange phrase
but I can’t explain this muscle tightening, creepy crawly feeling any better
way. It used to happen when I got my immunoglobulin infusions years ago,
because of the stimulation (in a good way) to my nervous system, which then
affects the muscles. Lately this phenomenon has come back in waves. My baby
stem cells are working extra hard. Eventually it settles down and I fall into a
deep slumber.
GIVEAWAY:
The Giveaway will be for one copy of the book This Is How I Saved My Life...and
-Handmade paper flowers sold at Dilli Haat bazaar in Delhi, India
-Ganesha statues, one of the most popular deities of India, the Hindu god of wisdom or prophecy, the god who removes obstacles
- Rangoli, a traditional design that dates back around 5,000 years as a decorative folk art in India. Rangoli is used for welcoming the Hindu deities such as Lakshmi, to bring good luck.
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I would love to read this book. It sounds amazing:)
ReplyDeleteWhat a great personal story with a message we can all use. Thanks for hosting this giveaway, I'd love to win a copy.
ReplyDeletecarlscott(at)prodigy(dot)net(dot)mx