HDYO International Representatives · HDYO International Representatives ... I will also join a meeting in Oslo the capital of Norway, ... compose video soundtrack music and direct

HDYO International RepresentativesHDYO International Representatives

HDYO has more information about HDavailable for young people, parents and

professionals on our site:

www.hdyo.orgwww.hdyo.org

Welcome to the home of our fantastic young HDYO International Representatives! The ‘Reps’

are a new resource in our volunteer team as of 2014. They are a team of young people from

around the world who are trained to do two things:

Raise awareness of support options for young people and families impacted by HD in the

region.

Tackle social stigma regarding HD in their local community through positive engagement with

the community

That positive engagement can come in various forms such as spreading awareness, contacting

local professionals and community members, giving talks about HDYO at local events and

working with HDYO to produce local awareness events in that region. The Representatives role

creates a new avenue for young people to get involved with HD and in turn, spread awareness,

improve knowledge in their region, and show other young people, families and the local

community a positive approach to HD.

Our Reps are available to attend events near you!Our Reps are available to attend events near you!Want a HDYO rep to attend an event in your region? Simply contact us using the box below and

let us know what you would like your local rep to attend and why. We will get back to you as

soon as we can!

[email protected]

Alternatively you can check out our list of reps below and contact the rep closest to you

geographically. We currently have reps in the following regions: Chile, England, France,

Germany, Norway, Ireland, N.Ireland, Poland, South Africa and Spain.

We will be training more reps in more locations as time goes on! If you’re interested in

becoming a rep then send a message to [email protected]

ChileChile

MariaMaria

I’m Maria from Chile, South América. I’m a

Social Worker currently working with

community leaders and neighbors in vulnerable

places. I enjoy spending time watching movies,

music, movies and biking. I have a family

impacted by HD. A beautiful, strong family with

my Mom and Dad, siblings and nephews, with a

history of relatives affected by HD which has

made us closer and whom I’m proud of each

day.

Tell us what you think about being a HDYOTell us what you think about being a HDYO

Rep and why you got involved with HDYO?Rep and why you got involved with HDYO?

As my dad says “I rather occupy myself than

mailto:[email protected]

stay just on preoccupying” that is way I want to be part of the HDYO team because I firmly

believe in HDYO’s project and how they approach to us in a positive and friendly way making a

global connection with people impacted by HD around the world, helping us cope with our

shared issues, making me feel I am not alone.

I want to spread awareness, especially in my country and South América where Huntington’s is

still just an inside family issue. I want to get young people involved and informed about good

stuff too.

Contact Maria

EnglandEngland

WayneWayne

My name is Wayne, I am 33 years young and I

have lived in England all my life. I work as an

Engineer for Virgin Atlantic, which keeps my

mind busy and active. It also allows me to see

the world with cheap flights!

My Mum has had HD for several years now and

is in residential care. I tested positive in 2011 for

the gene and currently have no symptoms. I

have 3 other siblings at risk of HD, but they are

much younger than me so have not tested.



Its early days at the moment but I have a few

ideas in terms of what a HDYO rep can do for

young people impacted by HD. I feel privileged

to help out a fantastic organisation and to help

others cope with HD.

I am involved as I have young siblings at risk and knowing how little support is out there has

motivated me to get involved and help where I can.

If I can help just one person in some way then I would be very happy, hopefully I can help many,

many more. I just want people to be aware of the support available and for them to know they

are not alone.

Contact Wayne

FranceFrance

EmilieEmilie

mailto:[email protected]?subject=Maria

mailto:[email protected]?subject=Wayne

I was born in Paris where I live. After a MD in

psychology, and a few years working within

ethnopsychiatry and social care services, I

decided to dedicate myself in writing. I am now

a novelist and an essayist.

In 2012, I founded a French and Belgium

working group, Dingdingdong, Institute for the

Co-production of Knowledge about HD, which

gather philosophers and artists in order to

create some alternative thoughts and path

about HD’s dilemmas. www.dingdingdong.org

I consider HD as a journey, and the people who

are affected with it as explorers. Their

knowledge is rare and precious for the rest of

society.



I am so grateful about HDYo… so for me it’s a natural choice to get involved into it. Among to

national associations, HDYo is really a crucial trans-national HD users movement and I am proud

to be, modestly, part of it.

In France, HDYo is unfortunately not very known yet. So this year, I will present HDYo to all the

French Associations. From there, I will try to be a facilitator between France associations and

HDYo. I hope some of the other associations will join me as an HDYo Rep, to strengthen the

acknowledgement about HDYo.

Contact Emilie

GermanyGermany

MichaelaMichaela

My name is Michaela, I’m 39 years old (as of

Feb 2014) and live in Stuttgart, Germany. I work

as an IT Coordinator for Daimler Trucks, Buses

and Vans. I grew up in a Huntington’s Disease

family. I was told about HD at the age of 15. My

Dad died of Huntington’s in 2002. HD has

always been a part of my life.



I like the idea to have local HDYO Reps all over the world to spread the word about HDYO, give

http://www.dingdingdong.org

mailto:[email protected]?subject=Emilie

HDYO a face and enable the local people to learn about HDYO.

I want to give as many speeches on youth support in Germany - including highlighting HDYO as

a major resource for young people. And I want to learn the needs of young people in Germany

and make a huge step to improve the available youth support in Germany.

Contact Michaela

NorwayNorway

ErlendErlend

Hello! my name is Erlend I come from a small

town northern Norway, Mosjøen. I’m 20 years

old. I play football in my spare time (every

week) I enjoy cycling in the summer and go to

the gym meet friends and work out. I also like

to spend time with friends and family. I’m a

student, studying industrial mechanics.

I was told about the disease when I was around

16 years old, I was tested for it when I was 18

and I have the genes, It was 50/50 and I got it

so I think that’s just a new challenge in my life,

but I know I can still have a good life even if I

had I have the genes.



I think that’s really great! I said yes for a reason, as I’m really excited to get more and more

involved with HDYO. I started as a hdyo.org translator after my first summercamp and became a

HDYO reps after the Barcelona YAWG meeting. This is something I really want to do.

I will do my best to show the local community where I live more about HDYO.org (Start with my

school, have a speech for the teachers and the students) I also want to give out hdyo.org

wristbands and t-shirt .

I want to start where I live, and do my best to spread awareness about HD, and the hdyo.org site

for young and less young people. I will also join a meeting in Oslo the capital of Norway, with

the Norwegian Huntington’s Association in April.

Contact Erlend

IrelandIreland

DavidDavid

mailto:[email protected]?subject=Michaela

mailto:[email protected]?subject=Erlend

My name is David and I’m 23 from Dublin, Ireland. I am the

HDYO international representative for the Republic of Ireland.

My day to day life consists primarily of music and having fun

one way or another! I am a musician and have been playing

music for as long as I can remember. I teach guitar lessons,

record and produce music videos, play bass in a band,

compose video soundtrack music and direct the Fingal Gospel

Choir. Busy times! During my time studying Music at Dundalk IT

I wanted to write a thesis on the effects of music therapy in a

health related area. When I read up on Huntington’s disease,

its symptoms really fit the beneficial description of music

therapy. After researching the benefits music therapy has on HD, I wanted to take it further. So I

joined the HD Association of Ireland, and I am now a board director. I will be using my position

to pitch ideas regarding music in the HD community.

Tell us what you think about being a HDYO Rep and why you got involved with HDYO?Tell us what you think about being a HDYO Rep and why you got involved with HDYO?

Being a HDYO rep is great in terms of the platform we are given to help the youth of the HD

community. It was truly an honour to even just be asked to the training day in Barcelona! I loved

every minute of it, and I found myself really wanting to pursue it in the future.

I hope to raise awareness to as many young people as possible across the country through

giving a presentation on HDYO and what it offers. A HDYO rep is like a signpost that directs

those affected by HD to somewhere they can understand and learn about their circumstances

appropriately and clearly. I really hope I can make a difference through this process!

Contact David

Northern IrelandNorthern Ireland

Sarah-LouiseSarah-Louise

Hi, my name is Sarah-Louise, I’m 24 years old, from Northern

Ireland. I am a newly qualified Psychiatric Nurse, currently

working with some HD patients receiving end of life care. I am

also a family member, as my grandmother had HD. As of yet

none of her 7 children have showed any symptoms of the

disease. I got involved with my local HD association as I hope

to become a HD specialist nurse sometime in the future. I am

also a newly appointed board member with The HDA Northern

Ireland and hope to help out as much as I can.

Tell us what you think about being a HDYO Rep and whyTell us what you think about being a HDYO Rep and why

you got involved with HDYO?you got involved with HDYO?

I am very excited to become a HDYO Rep and get involved with what’s happening all around

the world, as well as sharing new ideas about how we can support people in HD families, their

carers and give new insight to professionals about the illness.

mailto:[email protected]?subject=David

As a HDYO Rep, I hope to raise awareness of HD in my local area and across Northern Ireland

as whole. I would also like if The HDA Northern Ireland could work together with HDYO to

support families impacted by HD.

Contact Sarah-Louise

PolandPoland

MariannaMarianna

I’m Marianna from Poland. I’m a pharmacist and

love this job because it’s about helping people.

Privately I help Dad, who has HD, which is

tough at times but allows me to understand HD

family members better. In my free time I’m a

HDYO and Polish HDA volunteer which brings

me lots of satisfaction. I’m also a big fan of

traveling, reading the books and watching

Friends and Big Bang Theory episodes (let’s

face it, I’m kind of addicted…).



Getting involved in HDYO activities made me stronger. When you know about all these people

coping with HD every day, you realize that you are not alone. Also talking about HD makes me

more open and not as scared as at the beginning of my HD journey. Being a HDYO Rep is a

completely new way to tell as many people as possible about our wonderful Organisation (yea, I

mean HDYO!). Everybody should know that we are here to help young people who need the

special support and positive attitude for the hard days. I feel we have to spread the word about

HDYO all around the world!

My main goal is to reach the HD professionals who have not cared about supporting HD families

before. I know I have to keep reminding them that young people affected by HD have their

special needs and may find HDYO extremely useful (like I do!). Also I know it is important to

update Polish HD Families about what we do to encourage them not to hide HD topic anymore.

Contact Marianna

SpainSpain

NoeliaNoelia

mailto:[email protected]?subject=Sarah-Louise

mailto:[email protected]?subject=Marianna

Hi, my name is Noelia, I live in Madrid, Spain. I

am 20 years old. My grandma had HD and

several of my cousins are 50% risk for the

disease. My mum is not carrying the HD gen, so

I am not at risk myself. I am studying to be an

Speech and Language Therapist at the Univ.

Complutense of Madrid. I am a nutrition

technician.


I am Vice-President of the Spanish HD Association for Youth (AJH) and I had been a volunteer

for many years of the Spanish Huntington Association. I want to get many young people to get

to know and join the HDYO and the AJH to develop projects and activities together in Spain.

Contact Noelia

AllyAlly

British Columbia, CanadaBritish Columbia, Canada

My name is Ally, and I’m from Canada. I’ve been actively

involved with the HD community for about 6 years now,

and I really enjoy it. My mom passed away from HD, and 2

of out 3 of my sisters have been diagnosed with HD. I’m

currently finishing up my pharmacy degree, so I’m pretty

busy! On my down time, I like running, walking my dog,

doing yoga, and making crafts!



I’m excited about becoming an HDYO rep because it will

help me raise awareness in a more formal fashion. I am

also looking forward to giving presentations to the public!

Getting involved with HDYO seemed like a natural thing to

me to do as I’ve been actively involved with the HD

community in Canada for the past 6 years.

I hope to do presentations to health professionals and the general public, and raise more

awareness for HD.

Contact Ally

CatherineCatherine

Newfoundland, CanadaNewfoundland, Canada

mailto:[email protected]?subject=Noelia

mailto:[email protected]?subject=Ally

Hi there! My name is Catherine, I am 21 years old, from

Newfoundland, Canada. I just recently graduated from

Memorial University of Newfoundland with a Bachelor of

Nursing degree. Upon graduation, I started my career as a

Neurosurgery/Urology nurse. Huntington’s Disease has

been a part of my life ever since I can remember as my

grandmother started showing symptoms of HD when I was

just a baby.



I think the HDYO Representatives program is a fantastic

initiative and I’m so thrilled to be a part of it! I got involved

with HDYO to help spread awareness in my community and

to help eliminate the social stigma related to HD that still exists here in Newfoundland, Canada.

The HDYO Rep program has provided me with the skills and knowledge to achieve these goals.

In addition, it has allowed me to connect with HDYO Reps globally to share ideas. As a HDYO

rep I hope to spread HD awareness and eliminate social stigma regarding HD in my local

community.

Contact Catherine

ChelsieChelsie

Ontario, CanadaOntario, Canada

My name is Chelsie Legree. I am 22 years old. I

am from Arnprior, Ontario, Canada, but I am

currently finishing up my last year of Teacher’s

College at Nipissing University in North Bay,

Ontario, Canada. I will be a qualified teacher in

a month, if only there were jobs! I enjoy baking,

playing video games and have taken an interest

in art. I knew that HD was in my family, but only

found out that I was at risk when I was 18. I got

tested as soon as I could and found out that I

am gene-positive, pre-symptomatic. 1 out of 3

kids isn’t bad in my opinion.



I think being an HDYO Rep will be extremely rewarding. I wish it was around when I was going

through testing. After getting tested, I really struggled to find support because none of my

siblings were positive and my local chapter scared me because it was all people who already

had symptoms. I managed to dig deep, look past all the negative thoughts and find myself. I

want to be able to give information about services and resources for other young people.

mailto:[email protected]?subject=Catherine

I want to provide resources for young people and point them to the services that are available. I

don’t want any other young person to feel the way I felt during that time, which is why I think it is

important to be available for others.

Contact Chelsie

DestinyDestiny

Delaware, USADelaware, USA

Hi, my name is Destiny Hand. I’m 18 years old

and am currently still a high school student and

working with an elderly lady as my part time job.

I live in a state you may not think even exists…

That being Delaware. I love doing things

outdoors, taking pictures (of every and

anything), planning events, and helping others.

I’m pretty shy if you don’t know me, but I do

have a pretty crazy side… I’m not yet sure what

the plans are after I graduate, but would love to

get involved in some type of ministry- so I’m just

waiting on God’s direction. My mom passed

away from Huntington’s Disease when she was

only 38 and I became her care-taker for a

majority of my life. Yes, it was difficult, but I spent time with her that no one else had and I would

never trade that time for anything. Now, my 19 year old sister is showing symptoms and I feel

like my life is on replay. It’s a difficult thing to watch, but with God’s strength my family and I

make it through. I, as well as my other two brothers are also at risk. I have chosen not to be

tested at this point of time in my life because I don’t feel like it would benefit me. If I was tested

positive, I would probably become depressed and not be as active as I am, and if I tested

negative I would feel guilty because I would have to watch my siblings suffer (if other siblings

are positive) something that I somehow escaped. I have chosen to try to make something

positive out of a negative circumstance in my life. For quite a while I was angry that Huntington’s

was in my life. Now, I have accepted it, knowing I wouldn’t be who I am today without it, and

have chosen to get involved in the community as much as I can. I’m open about telling people

that my mom passed away from complications of the disease at an early age and that my sister

is now symptomatic. I also am working on organizing my second walk for Huntington’s Disease

in my area on May 17th! I encourage you all, involved with HD or not, to let people know that this

Disease exists and to try to bring it to a stop one step at a time!

Contact Destiny

EmilyEmily

Minnesota, USAMinnesota, USA

mailto:[email protected]?subject=Chelsie

mailto:[email protected]?subject=Destiny

My name is Emily Breen (formally Viau). I am 29

and I live in Minneapolis, MN with my husband

Michael. Professionally I am a Project Manager

at a technology company in the Minneapolis

area. I have been a volunteer with HDSA/HDYO

for 17 years since my mom was diagnosed with

HD when I was 12 years old. I have helped

coordinate our Hoopathon for the past 15 years

and I’m also involved in our COE fundraiser

dinner called the Blast along with many other

events. I am also in my 3rd year on the

Minnesota Chapter Board.


I decided to get involved as a Rep and I believe that there is more I can offer to the HD

community as a volunteer and there is a HUGE need to support, educate and empower the

young people in our community! HDYO is an amazing resource and group that I wholeheartedly

believe in. Living positively with HD in your life is an incredibly powerful message and I hope I

can help spread that message and make life just a little bit easier for even just 1 person that is

touch by this terrible disease.

As a rep I hope to educate people about HD and what HDYO is trying to accomplish. I hope to

tell as many people as I can about the amazing network of support that is out there and the

educational materials that are available to them. I have plans to speak at various Education

Days, Support Groups and Chapter events in my region.

Contact Emily

EmmyEmmy

Wisconsin, USAWisconsin, USA

My name is Emmy Lex and I am from Wisconsin,

in the United States. I am nineteen years old

and a sophomore in college at the University of

Wisconsin-Whitewater. I am getting a degree

that will license me to teach both elementary

education and special education for children

birth through third grade. I love to sing in my

free-time. My mom has Huntington’s Disease,

making me at-risk for inheriting it. Along with

my mom, I have 3 uncles who were positive and

they have had children that are now positive. It

runs throughout my whole family. This is where

my passion for Huntington’s Disease and

fighting to find a cure came from. Along with

being an HDYO Rep, I am on the Huntington’s Disease Society of America – WI Chapter Board

mailto:[email protected]?subject=Emily

and a member of the National Youth Alliance.


I love the idea of being an HDYO Rep and think that it is an amazing program and will benefit

many people. I got involved with HDYO because when my mom was diagnosed with

Huntington’s, I felt really alone and like there were no other people my age going through the

same thing. Through HDYO, youth can gain support and learn that they are not alone, which I

think is amazing.

As a rep, I hope to connect youth to others that are dealing with many of the same things that I

went through. I want to help youth that are impacted by Huntington’s Disease find the support

that they need and probably do not know is available for them. I want to make a difference.

Contact Emmy

ErikaErika

Washington, USAWashington, USA

I am an osteopathic medical student at Pacific Northwest University of Health

Sciences in Washington State. I grew up in Northwest Washington State. My

dad had HD and died when I was 11. At age 19 I tested negative for the

huntingtin gene expansion. My sister tested positive on the same day and

has been symptomatic since her mid-twenties. I try to make the most of every

day, maintain a positive attitude, and persevere through difficult situations. I

enjoy traveling with my family and cooking healthy, delicious food.


I am super excited about being an HDYO rep! Growing up at risk for HD often felt isolating and

there was so much uncertainty. I feel lucky to have the opportunity to facilitate support for

young people around the world and remind them they are not alone.

As an HDYO rep I am looking forward to sharing the hope I have for a better future for people

impacted by HD. I want to educate people about HD and remind everyone they are not alone in

this crazy adventure.

Contact Erika

JaclynJaclyn

Ontario, CanadaOntario, Canada

mailto:[email protected]?subject=Emmy

mailto:[email protected]?subject=Erika

My name is Jaclyn Skinner and I am from Ontario, Canada! I am

one of the most friendly and outgoing people you could meet

and love giving hugs � I currently work as an administrative

assistant for Hydro One and am working on climbing that

corporate ladder. My company is very supportive of giving back

to the community which gives me the opportunity to be part of

this HD community. I sit on the executive as the Public

Relations representative for YPAHD (Young People Affected by

Huntingtons Disease); I am a mentor in the Youth Mentorship

program and most recently, I’ve become a HDYO rep! I have

been impacted by HD my whole life, which makes this fight

against HD very close to my heart and why it is so easy for me

to be a part of so many groups. I love the HD family that I have

come to know and anticipate meeting more and more of you!


Being an HDYO Rep is an honour. It makes me feel good knowing that I’ve been recognized by

the HD community and what I have been doing is making a difference. That’s also a big reason I

became involved with HDYO – to make an even bigger difference with the help of people who

share that same dream. #unitethefight

My biggest goal of being an HDYO Rep is to unite the fight. Going to conferences and training

sessions just shows me that there are sooooo many of us around the world going through the

same things and looking for the same cure. There is power in numbers and I think if we can get

everyone on the same page with the same messages we could move mountains and be the last

generation that has to know what the effects of HD can bring.

Contact Jaclyn

LindsayLindsay

Ohio, USAOhio, USA

Hi! I’m Lindsay, I’m 26 and live in Cincinnati,

Ohio. I’m a registered nurse in the cardiac ICU

at Cincinnati Children’s hospital and also work a

few shifts a month in an adult OR on the cardiac

surgery team. I run full and half marathons to

fundraise for HD and next year hope to run the

NYC marathon as a part of the HDSA team. I’m

getting married this December, have a husky,

and enjoy naps. I like to consider myself one of

the “original” members of the NYA and have

been a part of tha in some way since 2002

when I went to my first national convention. I’m

involved and soon to be on the board of the

Ohio Valley chapter. My father is in late stages

mailto:[email protected]?subject=Jaclyn

of HD, and both my grandfather and great-grandmother also had HD. I tested gene-negative in

October of 2011 and have made it my mission to be an advocate for not only HD itself, but for

the families and youth affected. I vowed to live my life to the fullest, no matter my results, and

am doing just that!


I think being a HDYO rep is the perfect thing for me because it’s being there and giving hope

and showing the families and youth affected by HD that there is information out there and others

in situations just like theirs – including me! I got involved as part of my personal mission to help

other families and youth in my part of the country.

I hope to help bring some positive light and relief to families as a rep. Showing them the

website, giving them the information out there for parents to help talk to their kids and giving

kids a place to ask questions and find information themselves at age appropriate levels is a

wonderful opportunity. I know that growing up in a family with HD can be overwhelming and it

feels like no one could possibly understand, but there’s a whole set of resources and

connections that we can provide to help these young people and their families cope.

Contact Lindsay

SavannahSavannah

Colorado, USAColorado, USA

I am a California native, currently living and

working in Denver, CO. While I enjoy working at

Trader Joe’s, I have been searching for a

chance to work for a cause closer to my heart.

HD has impacted my family for over 15 years

now, since my dad first started showing

symptoms. While it has been a heartbreaking

process, growing up with my dad and watching

his progression with HD has stimulated within

me a greater appreciation for my life, and the

beautiful people and things in it. I love meeting

and connecting with new people, exploring new places, and being outdoors whenever possible.


Being an HDYO Rep is a great opportunity to connect with fellow youth in my community who

are impacted by HD. Not only do I gain connections with others, through shared feelings and

experiences regarding similar family histories, I also have the resources to help these folks find

the help they may need.

As an HDYO Rep, I aim to help as many community members as possible, by providing them

with important resources, knowledge, and hope that they may otherwise would not have access

to.

mailto:[email protected]?subject=Lindsay

Contact Savannah

SethSeth

Massachusetts, USAMassachusetts, USA

My name is Seth and I am 23 years old,

currently living in Natick, MA. I graduated from

UMass Amherst in 2013 with a degree in sport

management. I have been involved with HD

ever since my mom has been diagnosed with

the disease for about nine years now. I have

been actively involved in the HD community,

doing my own hoops fundraisers for HD as well

as supporting other local fundraisers. I am

currently the President of the MA Chapter for

HDSA in the US and the co-chair of the National

Youth Alliance (NYA); the largest youth

organization for young people impacted by HD

in the US.

In my spare time I like to hangout with my friends, play basketball, go on runs, spend time with

my family, or play outside with my dog. My dog is a four year old black lab mix and loves to meet

new people!


I think being a HDYO Rep is a great opportunity for the young people in the US who are already

involved in the NYA, to collaborate more with HDYO. I got involved because I find it important to

unite all youth organizations that are fighting for the same cause, which is to support young

people impacted by HD.

I hope to raise more awareness about young people who are impacted by HD. I think it is

important to realize that adults are not the only people involved with HD and that there needs to

be more support and resources for young people.

Contact Seth

JordanJordan

Mississippi, USAMississippi, USA

mailto:[email protected]?subject=Savannah

mailto:[email protected]?subject=Seth

Hey ya’ll! I’m Jordan, 25 year old HD Advocate. I have been

a part of the HD Community for 11 years, being involved in

chapters, support groups and national level organizations

since I was 13 and attended my first HDSA conference in

Houston, Texas. After growing up and going to school in

Austin, Texas I now live in Indianola, Mississippi in the heart

of the Delta.



Being an HDYO rep is such a great opportunity, giving

young people access to an international organization

tailored to helping young people from a young person’s

point of view. I wanted to be able to reach out to those

people whom may not have a connection to the HD community, and provide the information

needed to access it.

I hope to provide the Millennial Generation with information concerning HD and how they can

give themselves the best possible lives being an HD advocate

Contact Jordan

This document was downloaded from the HDYO website at https://en.hdyo.org/fri/about/273

Advice received via the HDYO web site should not be relied upon for personal, medical, legal or financialdecisions and you should consult an appropriate professional for specific advice tailored to your situation.

HDYO is licensed under a Creative Commons license.

http://hdyo.org

mailto:[email protected]?subject=Jordan

Documents

HDYO International Representatives · HDYO International Representatives ... I will also join a meeting in Oslo the capital of Norway, ... compose video soundtrack music and direct