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Homepage ART4RARE – Annual Rare Art Contest
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  • « 3rd Annual Anniversary
  • Science4Rare 2023 »

ART4RARE – Annual Rare Art Contest

January 30, 2022
By
1 Comment
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Announcement of Art4Rare awards

    ART4RARE 2023

Exiciting Prizes to win
Last day to submit: Feb 10th, 2023

Result will be announced on Internatinal Rare desease day. 28 feb 2023

Age Categories

  • All age groups are welcome to Participate.

Registration 2023  : https://bit.ly/art4rare2023

About the Event

IndoUSrare invites submissions from artists all over the globe for our Annual Rare Art Contest, ART4RARE 2023.

This year’s theme is “All things Rare.” Artwork submitted should represent whatever the word rare means to you – it could be anything from a rare or exotic plant, animal, a rare event like a shooting star or other astronomical event, a rare geological formation, or even abstract art representing “RARE”.

Submissions are accepted till 10th February 2023, 11:59 pm local time, and winners will be announced on Rare Disease Day at IndoUSrare.

Feel free to unleash the inner artist in you, for a good cause.

Let’s Roar for Rare!!!

Guidelines

  • The submission must be original work by the participant for ART4RARE which has not been published elsewhere. It should not be a replica of another person’s art.
  • Art (Sketches, Drawings, or paintings) can be of any medium (Pencil, Crayons, Acrylic, Oil, or watercolor). Digital Artwork will not be accepted.
  • The size of the artwork image should be either 8 x10 inches or 10 x12 inches.
  • Please include a title for your artwork.
  • Please prepare a one-paragraph description (400 words) about your artwork to be filled in during submission. You can describe how you feel your submission fits into the theme of the contest.
  • The artwork created should be uploaded using the submission form as a PDF, jpg, or png file.
  • The uploaded file size should not exceed 10 MB.
  • Name your file as follows: ‘Title of the artwork_Artist Full Name _ART4RARE2023‘
  • You must register for ART4RARE 2023 to be able to submit your artwork. The instructions (the web form details) for submission will be emailed to you once you purchase the Eventbrite ticket.
  • By registering, you express consent for the submission to be used by IndoUSrare for display on our website, social media, etc.
  • Please note that IndoUSrare reserves the right to reject any submission without notice. This could be for reasons such as non-payment of fees and submission which are not as per guidelines.
  • Submissions are accepted till 10 February 2023, 11:59 pm local time.

Any questions?

Contact us at admin@indousrare.org

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Copyright ©2022 Indo US Organization for Rare Diseases. All rights reserved. IndoUSrare is a registered 501(c)(3) charity organization.
MS. KANAN LATHI

Kanan Lathia is an Ambassador and scientific consultant at Indousrare.She has spent 20+ years as a research scientist focusing on neurodegenerative diseases, cancer, and HIV. She has also worked as a project manager supporting teams in building brain maps of the first 1000 days of babies. Kanan’s passion for rare diseases is driven by a personal cause. Her work with Dup15q Alliance strengthened her passion for giving back to rare disease families. Kanan hopes to scale the organization’s efforts by securing funding and building a patient alliance membership program. Kanan loves yoga and spending time between the US and India.

 Dr. Krishna Ramaswamy

Dr. Krishna Ramaswamy is a life science professional with experience in research, management consulting, and business development in academia and industry. She has a Ph.D. in Biological Sciences from University at Buffalo, SUNY, and pursued postdoctoral research in cell biology from the University of Southern California, Los Angeles. She has worked as a consultant for the biotech/pharma industry and worked with Dr. Harsha and ORDI in the past for about 2 years. Dr. Krishna currently resides in Hyderabad India and has a keen interest in the rare diseases space and would like to bring awareness about the various diseases, diagnoses and treatments that are available and those in the pipeline. She first began working in the rare disease space during her postdoctoral training and has worked on peroxisome biogenesis disorders under the guidance of Dr. Joe Hacia at USC.

Ms. Neeraja

Neeraja is in her junior year of high school, studying at a School in Gurgaon, India. She has completed all 8 grades in a set of vocal examinations conducted by Trinity College as the captain of the Student Council in her school, currently serving the post of House Captain. Neeraja aims to find solutions to the problems associated with the fields of healthcare, technology, and sustainable development. She is passionate about teenage welfare and has founded a youth-centric organization called ‘Discover Yourself’ through which she aims to inspire, and collaborate with young people across the world and wants to bring awareness regarding various teenage and adolescent issues

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