Professional Documents
Culture Documents
Samyuktha Shanthakumar
30 November 2023
Evidence of Learning: A Molecule Away from Madness: Tales of the Hijacked Brain by Sara
Manning Peskin
For my second Evidence of Learning, I am writing about the book A Molecule Away from
Madness: Tales of the Hijacked Brain by Sara Manning Peskin. This book discusses minuscule
but paramount molecules in our brain and how they can be triggered to cause life-altering
diseases like Huntington's disease, Parkinson's disease, Pick's disease, etc. The author
categorizes these molecules as mutants, rebels, invaders, and evaders. Mutants are altered
sequences of DNA. DNA is a long, chainlike molecule made of four bases: adenine, cytosine,
guanine, and thymine. These bases are abbreviated as A, C, G, and T. These are arranged in a
specific order throughout a person's DNA molecule. Even when a minute part of this molecule is
altered, it can cause life-shortening diseases. Think of the DNA as computer code and the
alterations as typos in the computer code. These typos would cause the program to self-destruct.
Like computer code, DNA contains instructions that tell enzymes how and where each protein
should be made throughout our body. If there are alterations in the DNA molecule, the enzymes
that make new proteins will read the incorrect directions and produce the wrong protein in the
bad part of the body. Over time, as these faulty proteins accumulate in the body and perform
The following molecules in this list are rebels. Rebels are aberrant proteins. Under
normal circumstances, these proteins take instructions from the DNA and work accordingly.
However, some proteins can be triggered to rebel in the body by attacking essential functions,
processes, and organs in our body. If we think about DNA as the computer code, then the
proteins would be the people and infrastructure that bring the legend to life to use in real life.
When these rebellious proteins attack our brains, it causes symptoms like confusion,
hallucinations, and dementia. The last two molecules on the list are characterized as invaders and
evaders. Invaders are molecules that enter our brains when they are unwelcome or unnecessary
and affect essential processes in our brains. Evaders are small molecules that are not available in
our brains when they are needed. One or more criminal molecules mentioned above affect the
There were many neurological diseases discussed in this book, but the disease that piqued
my interest was Huntington's disease. The author begins the chapter on this disease by describing
the setting of a Huntington's disease clinic, where a 26-year-old woman named Amelia Elman
was waiting to get her results back on whether she has Huntington's or not. Amelia's mother had
passed away from Huntington's disease a year ago. Her mother's death was slow, excruciating,
and lasted for a decade. Amelia began noticing her early Huntington's symptoms in her mom
when she moved to a motel with her mom. Her mom's arms would move and jerk unpredictably,
knocking down objects from countertops or hitting the sides of furniture. Cooking became an
arduous task for her mom. Her mom would often drop silverware or burn herself due to
uncontrollable movements, and when those movements became intense, she collapsed to the
floor and looked at the ceiling. A couple of years went by, and Amelia transferred her mom to a
Shanthakumar 3
nursing home. Now, Amelia began noticing late-stage Huntington's symptoms like more
prominent jerking movements, hallucinations, and inability to speak in her mother. Her mom was
convinced that she owned a Walmart and that she and Amelia were still living together. Amelia's
mom soon lost her ability to speak. She was quickly unable to swallow food or liquids properly,
and this resulted in frequent aspiration (accidentally inhaling an object or fluid into the airways)
and caused bouts of pneumonia. Amelia's mother passed away one day. Amelia learned that
Huntington's disease was genetically inherited and that she has a 50% chance of inheriting it.
Amelia soon learns that she has Huntington's as well. She decides to train her body and mind as
strong as they can be to handle the hurdles that the disease throws her. She also begins traveling
the world to see places and meet people while she still can.
After describing Amelia's story, the author discusses a group of researchers who invented
a way to test for Huntington's disease. In 1968, a 23-year-old woman named Nancy Wexler
created workshops with groups of scientists to find out a way to cure Huntington's disease. In
1979, scientists from one of Nancy's workshops figured out a way to identify Huntington's
disease. They stated that when DNA is inherited, genes that are close together in a chromosome
are likely to be inherited together. Instead of finding one specific gene, they can look for a region
of the DNA where Huntington's gene is potentially present. The scientists decided to use tiny
molecular scissors that could cut the region where Huntongton's gene is supposed to be. These
molecular scissors cut the gene so that the DNA region with Huntington's disease would appear
in a different length than the region without Huntington's disease. This vital discovery paved the
I was assigned this book as a reference for the HOSA Medical Reading competition.
When I finished reading this book, I felt content that I had learned a lot from it that would help
me with my competition and my PCIS project. There were many chapters in the book where the
concept of neuroplasticity played an important role, which helped me find ideas I could
incorporate into my PCIS project. This book helped me discover my interest in researching
Huntington's disease and how it affects the brain over time. I will use the information from this
Work Cited
Peskin, Sara Manning. A Molecule Away from Madness: Tales of the Hijacked Brain. W. W.