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“Navigating Genetic Disease Testing: A Personal Story” | Seth Rotberg | TEDxNatick


neurologist said Seth your test results

neurologist said Seth your test results came back positive for Huntington’s

came back positive for Huntington’s

came back positive for Huntington’s disease I blocked out everything the

disease I blocked out everything the

disease I blocked out everything the neurologist had to say after that

neurologist had to say after that

neurologist had to say after that because I knew I was destined to slowly

because I knew I was destined to slowly

because I knew I was destined to slowly deteriorate both physically and mentally

deteriorate both physically and mentally

deteriorate both physically and mentally just like my mom now minutes before this

just like my mom now minutes before this

just like my mom now minutes before this I was your typical 20 year old college

I was your typical 20 year old college

I was your typical 20 year old college sophomore happy with lots of friends I

sophomore happy with lots of friends I

sophomore happy with lots of friends I loved playing soccer and basketball and

loved playing soccer and basketball and

loved playing soccer and basketball and going out on the weekends but especially

going out on the weekends but especially

going out on the weekends but especially going out on the weekends but in my head

going out on the weekends but in my head

going out on the weekends but in my head I couldn’t help but think that I just

I couldn’t help but think that I just

I couldn’t help but think that I just tested positive for Huntington’s disease

tested positive for Huntington’s disease

tested positive for Huntington’s disease now deep down inside I knew I already

now deep down inside I knew I already

now deep down inside I knew I already had it but this was just confirmation

had it but this was just confirmation

had it but this was just confirmation that it was for real and I was in shock

that it was for real and I was in shock

that it was for real and I was in shock so what is Huntington’s disease which is

so what is Huntington’s disease which is

so what is Huntington’s disease which is also known as HD I’ll paint you a

also known as HD I’ll paint you a

also known as HD I’ll paint you a picture my mom had poor balance and

picture my mom had poor balance and

picture my mom had poor balance and wobbly movements often tripping and

wobbly movements often tripping and

wobbly movements often tripping and falling over we had neighbors who

falling over we had neighbors who

falling over we had neighbors who thought she was just just a drunk she

thought she was just just a drunk she

thought she was just just a drunk she had these severe mood swings for one

had these severe mood swings for one

had these severe mood swings for one minute she was fine and then the next

minute she was fine and then the next

minute she was fine and then the next she was frustrated or angry or depressed

she was frustrated or angry or depressed

she was frustrated or angry or depressed and finally there was this cognitive

and finally there was this cognitive

and finally there was this cognitive decline which results in short-term

decline which results in short-term

decline which results in short-term memory loss concentration losing loss of

memory loss concentration losing loss of

memory loss concentration losing loss of concentration decision-making among

concentration decision-making among

concentration decision-making among other things HD is a rare neurological

other things HD is a rare neurological

other things HD is a rare neurological genetic disease as if someone has ALS

genetic disease as if someone has ALS

genetic disease as if someone has ALS Alzheimer’s and Parkinson’s all at once

Alzheimer’s and Parkinson’s all at once

Alzheimer’s and Parkinson’s all at once and the worst part about it is that

and the worst part about it is that

and the worst part about it is that there is no cure once a person starts

there is no cure once a person starts

there is no cure once a person starts showing symptoms the average lifespan is

showing symptoms the average lifespan is

showing symptoms the average lifespan is 10 to 20 years my mom was slowly dying

10 to 20 years my mom was slowly dying

10 to 20 years my mom was slowly dying of this disease was only 49 years old

of this disease was only 49 years old

of this disease was only 49 years old and there was nothing I could do about

and there was nothing I could do about

and there was nothing I could do about it besides watching her clock slowly

it besides watching her clock slowly

it besides watching her clock slowly tick down I first learned about my mom’s

tick down I first learned about my mom’s

tick down I first learned about my mom’s condition when I was about 15 years old

condition when I was about 15 years old

condition when I was about 15 years old but like most teens I was too focused on

but like most teens I was too focused on

but like most teens I was too focused on the present to worry about the future in

the present to worry about the future in

the present to worry about the future in fact I felt like I was in denial and I

fact I felt like I was in denial and I

fact I felt like I was in denial and I was often embarrassed out in public with

was often embarrassed out in public with

was often embarrassed out in public with my mom do to her slurred speech and

my mom do to her slurred speech and

my mom do to her slurred speech and wobbly movements and would even stay at

wobbly movements and would even stay at

wobbly movements and would even stay at my friend’s houses just to get away it

my friend’s houses just to get away it

my friend’s houses just to get away it wasn’t until I went to college that it

wasn’t until I went to college that it

wasn’t until I went to college that it really hit me I have a 50/50 chance of

really hit me I have a 50/50 chance of

really hit me I have a 50/50 chance of inheriting this disease and ending up

inheriting this disease and ending up

inheriting this disease and ending up one day just like my mom a simple flip

one day just like my mom a simple flip

one day just like my mom a simple flip of a coin heads I win tails I lose I

of a coin heads I win tails I lose I

of a coin heads I win tails I lose I just didn’t know what side it was going

just didn’t know what side it was going

just didn’t know what side it was going to be because I had not been tested yet

to be because I had not been tested yet

to be because I had not been tested yet like most people and families who carry

like most people and families who carry

like most people and families who carry a fatal genetic disease so although I

a fatal genetic disease so although I

a fatal genetic disease so although I wasn’t ready to get tested I felt like I

wasn’t ready to get tested I felt like I

wasn’t ready to get tested I felt like I still needed to do something so my

still needed to do something so my

still needed to do something so my freshman year in college my friend Max

freshman year in college my friend Max

freshman year in college my friend Max and I decided to put on his throne

and I decided to put on his throne

and I decided to put on his throne through Baskerville charity event called

through Baskerville charity event called

through Baskerville charity event called hoops for Huntington’s to raise money

hoops for Huntington’s to raise money

hoops for Huntington’s to raise money and awareness for the disease you could

and awareness for the disease you could

and awareness for the disease you could say this was my way of coping not

say this was my way of coping not

say this was my way of coping not thinking about testing and ultimately

thinking about testing and ultimately

thinking about testing and ultimately just keeping busy but I couldn’t help

just keeping busy but I couldn’t help

just keeping busy but I couldn’t help but still think about it because of the

but still think about it because of the

but still think about it because of the impact it would have on my future no

impact it would have on my future no

impact it would have on my future no matter which side of the coin would come

matter which side of the coin would come

matter which side of the coin would come up do I want to get married and have

up do I want to get married and have

up do I want to get married and have kids what about buying a house or

kids what about buying a house or

kids what about buying a house or traveling around the world what about my

traveling around the world what about my

traveling around the world what about my career plans these were things that were

career plans these were things that were

career plans these were things that were constantly on my mind and I needed to

constantly on my mind and I needed to

constantly on my mind and I needed to know it was mentally draining on a daily

know it was mentally draining on a daily

know it was mentally draining on a daily basis and I was tired of living with the

basis and I was tired of living with the

basis and I was tired of living with the unknown so I got tested

unknown so I got tested

unknown so I got tested I thought I was prepared for the news

I thought I was prepared for the news

I thought I was prepared for the news but in fact I wasn’t because minutes

but in fact I wasn’t because minutes

but in fact I wasn’t because minutes before going into that exam room

before going into that exam room

before going into that exam room I was just Seth but now I was HD Seth

I was just Seth but now I was HD Seth

I was just Seth but now I was HD Seth and I had to figure out how HD Seth

and I had to figure out how HD Seth

and I had to figure out how HD Seth wanted to live his life one thing I knew

wanted to live his life one thing I knew

wanted to live his life one thing I knew I couldn’t tell my family my mom was

I couldn’t tell my family my mom was

I couldn’t tell my family my mom was still alive at the time and I knew she’d

still alive at the time and I knew she’d

still alive at the time and I knew she’d feel terribly guilty knowing she passed

feel terribly guilty knowing she passed

feel terribly guilty knowing she passed along this disease to her son my dad was

along this disease to her son my dad was

along this disease to her son my dad was a caregiver for my mom and I didn’t want

a caregiver for my mom and I didn’t want

a caregiver for my mom and I didn’t want to feel like another burden to him and

to feel like another burden to him and

to feel like another burden to him and then there was my older sister and

then there was my older sister and

then there was my older sister and because it’s a genetic disease I didn’t

because it’s a genetic disease I didn’t

because it’s a genetic disease I didn’t want her to feel pressured to also get

want her to feel pressured to also get

want her to feel pressured to also get tested so I told a few friends who were

tested so I told a few friends who were

tested so I told a few friends who were very helpful and supportive throughout

very helpful and supportive throughout

very helpful and supportive throughout the process I had one friend who came

the process I had one friend who came

the process I had one friend who came with me for my results and the rest I

with me for my results and the rest I

with me for my results and the rest I told on my hour-and-a-half car ride back

told on my hour-and-a-half car ride back

told on my hour-and-a-half car ride back to college so without knowing it I put

to college so without knowing it I put

to college so without knowing it I put myself in this genetic disease closet I

myself in this genetic disease closet I

myself in this genetic disease closet I shut the door and I hid my results for

shut the door and I hid my results for

shut the door and I hid my results for my family and most of the world six

my family and most of the world six

my family and most of the world six months one year two years went by I was

months one year two years went by I was

months one year two years went by I was still that typical college kid but now I

still that typical college kid but now I

still that typical college kid but now I was more actively involved in the HD

was more actively involved in the HD

was more actively involved in the HD community I joined a few HD

community I joined a few HD

community I joined a few HD organizations I was raising money and

organizations I was raising money and

organizations I was raising money and awareness and supporting young people

awareness and supporting young people

awareness and supporting young people and families impacted by the disease and

and families impacted by the disease and

and families impacted by the disease and everyone just assumed I was doing this

everyone just assumed I was doing this

everyone just assumed I was doing this because of my mom my senior in college

because of my mom my senior in college

because of my mom my senior in college in fact the day before my last semester

in fact the day before my last semester

in fact the day before my last semester my good friend Jake unexpectedly died in

my good friend Jake unexpectedly died in

my good friend Jake unexpectedly died in an accident in his high school yearbook

an accident in his high school yearbook

an accident in his high school yearbook there’s this quote that he embodied so

there’s this quote that he embodied so

there’s this quote that he embodied so much his parents put it on his headstone

much his parents put it on his headstone

much his parents put it on his headstone this quote said live as if you were to

this quote said live as if you were to

this quote said live as if you were to die tomorrow learn as if you were to

die tomorrow learn as if you were to

die tomorrow learn as if you were to live forever so I thought how can I keep

live forever so I thought how can I keep

live forever so I thought how can I keep Jake’s memory alive by living my life to

Jake’s memory alive by living my life to

Jake’s memory alive by living my life to the fullest

now a short time after this I lost

now a short time after this I lost another friend Megan who had a version

another friend Megan who had a version

another friend Megan who had a version of HD and passed away at the age of 26

now Megan was very open about her story

now Megan was very open about her story and was doing as as much as she could to

and was doing as as much as she could to

and was doing as as much as she could to raise money and awareness for the

raise money and awareness for the

raise money and awareness for the disease so I thought holy crap I just

disease so I thought holy crap I just

disease so I thought holy crap I just lost two friends gone way too soon why

lost two friends gone way too soon why

lost two friends gone way too soon why do I need to continue to hide my HD

do I need to continue to hide my HD

do I need to continue to hide my HD results despite Megan and Jake’s

results despite Megan and Jake’s

results despite Megan and Jake’s circumstances their positive outlook on

circumstances their positive outlook on

circumstances their positive outlook on life inspired me this was my turning

life inspired me this was my turning

life inspired me this was my turning point to finally come out of that

point to finally come out of that

point to finally come out of that genetic disease closet and go from being

genetic disease closet and go from being

genetic disease closet and go from being HD Seth to just plain old Seth but first

HD Seth to just plain old Seth but first

HD Seth to just plain old Seth but first I had to tell my dad and my sister I

I had to tell my dad and my sister I

I had to tell my dad and my sister I decided to tell them separately and I

decided to tell them separately and I

decided to tell them separately and I started with my dad I vividly remember

started with my dad I vividly remember

started with my dad I vividly remember walking into the living room sitting on

walking into the living room sitting on

walking into the living room sitting on the couch across from him and telling

the couch across from him and telling

the couch across from him and telling him I had something important to tell

him I had something important to tell

him I had something important to tell him after a long silence he looked at me

him after a long silence he looked at me

him after a long silence he looked at me and said alright Seth what is it what do

and said alright Seth what is it what do

and said alright Seth what is it what do you need to tell me dad

you need to tell me dad

you need to tell me dad I tested positive for Huntington’s

I tested positive for Huntington’s

I tested positive for Huntington’s disease

okay that’s all you’re gonna say he then

okay that’s all you’re gonna say he then said Seth researchers are making great

said Seth researchers are making great

said Seth researchers are making great progress and soon enough there’s going

progress and soon enough there’s going

progress and soon enough there’s going to be a cure now I told my dad I didn’t

to be a cure now I told my dad I didn’t

to be a cure now I told my dad I didn’t want mom to know about this so we both

want mom to know about this so we both

want mom to know about this so we both agreed not to tell her but it was so

agreed not to tell her but it was so

agreed not to tell her but it was so reassuring to know that my dad was gonna

reassuring to know that my dad was gonna

reassuring to know that my dad was gonna stick by my side just like he did with

stick by my side just like he did with

stick by my side just like he did with him with my mom so one down one to go

him with my mom so one down one to go

him with my mom so one down one to go I knew telling my sister was going to be

I knew telling my sister was going to be

I knew telling my sister was going to be easy but in fact I was wrong after

easy but in fact I was wrong after

easy but in fact I was wrong after telling her she had a few questions but

telling her she had a few questions but

telling her she had a few questions but was very loving and supportive but was

was very loving and supportive but was

was very loving and supportive but was shocked her most like most people was

shocked her most like most people was

shocked her most like most people was that I kept this a secret

that I kept this a secret

that I kept this a secret for two whole years now I realized this

for two whole years now I realized this

for two whole years now I realized this it was such a big mistake

it was such a big mistake

it was such a big mistake and if I could go back in time I would

and if I could go back in time I would

and if I could go back in time I would tell my dad my sister from day one

tell my dad my sister from day one

tell my dad my sister from day one because after telling them it was a huge

because after telling them it was a huge

because after telling them it was a huge sigh of relief and I felt like a weight

sigh of relief and I felt like a weight

sigh of relief and I felt like a weight just lifted off my shoulder I felt like

just lifted off my shoulder I felt like

just lifted off my shoulder I felt like a new person a new Seth I was motivated

a new person a new Seth I was motivated

a new person a new Seth I was motivated inspired and hopeful and I knew what I

inspired and hopeful and I knew what I

inspired and hopeful and I knew what I wanted to do in life which was share my

wanted to do in life which was share my

wanted to do in life which was share my HD journey and be a mentor to young

HD journey and be a mentor to young

HD journey and be a mentor to young people who face some type of adversity

people who face some type of adversity

people who face some type of adversity in life whether it’s HD related or

in life whether it’s HD related or

in life whether it’s HD related or another challenging circumstance helping

another challenging circumstance helping

another challenging circumstance helping young people is what makes me happy and

young people is what makes me happy and

young people is what makes me happy and who I am today

who I am today

who I am today just Seth not long after telling my dad

just Seth not long after telling my dad

just Seth not long after telling my dad and my sister I got a tattoo and here it

and my sister I got a tattoo and here it

and my sister I got a tattoo and here it is

is

is live as if you were to die tomorrow

live as if you were to die tomorrow

live as if you were to die tomorrow learn as if you were to live forever

learn as if you were to live forever

learn as if you were to live forever this is my constant reminder that life

this is my constant reminder that life

this is my constant reminder that life is too short and to take nothing for

is too short and to take nothing for

is too short and to take nothing for granted

a few years ago my mom lost her 17-year

a few years ago my mom lost her 17-year battle to this devastating disease she

battle to this devastating disease she

battle to this devastating disease she was and still is my inspiration brave

was and still is my inspiration brave

was and still is my inspiration brave and always had a smile on her face to go

and always had a smile on her face to go

and always had a smile on her face to go along with her sense of humor this

along with her sense of humor this

along with her sense of humor this journey is my journey but it’s not

journey is my journey but it’s not

journey is my journey but it’s not unique I’m one of millions of people who

unique I’m one of millions of people who

unique I’m one of millions of people who have to decide whether or not they want

have to decide whether or not they want

have to decide whether or not they want to get tested for genetic disease if you

to get tested for genetic disease if you

to get tested for genetic disease if you happen to be one of them remember that

happen to be one of them remember that

happen to be one of them remember that this is and should be a very personal

this is and should be a very personal

this is and should be a very personal decision because of the impact it will

decision because of the impact it will

decision because of the impact it will have on your future now having been

have on your future now having been

have on your future now having been there done that there are three things

there done that there are three things

there done that there are three things I’ve learned that I would like to share

I’ve learned that I would like to share

I’ve learned that I would like to share first if you can work with the genetic

first if you can work with the genetic

first if you can work with the genetic counselor and a neurologist who

counselor and a neurologist who

counselor and a neurologist who specializes in this field do it with

specializes in this field do it with

specializes in this field do it with their knowledge it will make the process

their knowledge it will make the process

their knowledge it will make the process a lot more manageable and easier not

a lot more manageable and easier not

a lot more manageable and easier not easy but easier the second thing

easy but easier the second thing

easy but easier the second thing talk to your family and close friends

talk to your family and close friends

talk to your family and close friends about it from day one I realized after

about it from day one I realized after

about it from day one I realized after telling my dad my sister I was just more

telling my dad my sister I was just more

telling my dad my sister I was just more comfortable and I didn’t have to hide in

comfortable and I didn’t have to hide in

comfortable and I didn’t have to hide in that genetic disease closet and finally

that genetic disease closet and finally

that genetic disease closet and finally when things get tough remember that each

when things get tough remember that each

when things get tough remember that each day is a new day and you have the

day is a new day and you have the

day is a new day and you have the opportunity to make the most of it we

opportunity to make the most of it we

opportunity to make the most of it we all have choices in life we have to make

all have choices in life we have to make

all have choices in life we have to make some are easy some are hard the harder

some are easy some are hard the harder

some are easy some are hard the harder they are the more support we need to

they are the more support we need to

they are the more support we need to reach out and ask for it find your motto

reach out and ask for it find your motto

reach out and ask for it find your motto find your reason and hey maybe get a

find your reason and hey maybe get a

find your reason and hey maybe get a tattoo

tattoo

tattoo thank you

thank you

thank you [Applause]

[Applause]

[Applause] [Music]

”

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