• Menu
  • Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Before Header

  • Home
  • About Us
    • Our Vision, Mission and Values
    • How We Help
    • Our Trustees
    • Our Staff
    • Our Regional Representatives
    • Our Professional Board
    • Small Grant Applications
    • Annual Reports
  • Blog
  • Shop
  • My Basket
  • Contact Us
donate

Smith-Magenis Syndrome Foundation UK logo

Connecting Families | Raising Awareness | Building Futures

Header Right

Smith-Magenis Syndrome Foundation UK

Connecting Families | Raising Awareness | Building Futures

Registered UK Charity 1072573 (CIO 1186647) | Registered Scottish Charity SC044841

  • Home
  • About Us
    • Our Vision, Mission and Values
    • History of the Foundation
    • Meet the Trustees
    • Meet the Staff
    • Our professional board
    • Regional Representatives
    • How We Help
    • Small Grant Applications
    • Annual Reports
  • What is SMS?
    • SMS Through our Logo
    • Sunlight and Nightshade
    • Sweet Dreams and Survival
    • That Defining Moment
    • Bright Stars Shining a Light
    • Frequently asked questions
    • Health
  • Information
    • Emergency hospital documents for download
    • Documents to Download
    • External links
    • Videos
  • Get Involved
    • Fundraising Ideas
    • Donate
    • Support My Smile Campaign
  • News
    • Newsletters
  • Blog
  • Become a Member
    • Professional Membership
  • Shop
  • Contact Us
  • My Basket
  • What is SMS?
    • Overview & Characteristics
    • Diagnosis
    • SMS Personality
    • Sleep Matters
    • Living with SMS
    • Health
    • Frequently asked questions
  • Information
    • Emergency hospital documents for download
    • Information
    • Documents to Download
    • External links
    • Videos
  • Research
  • Get Involved
    • Get Involved
    • Co-op Local Community Fund
    • Fundraising Ideas
    • Support My Smile Campaign
    • Become a Regular Donor
    • Donate
  • News & Events
    • Newsletters
    • SMS Conference 2021
  • Become a Member
    • Family Membership
    • Professional Membership

Natasha Craven Shortlisted for ‘Best Student Contribution’ to a Small to Medium-sized Employer award!

January 5, 2021

Natasha Craven, who joined the Smith-Magenis Syndrome Foundation UK team in October 2020, has successfully been shortlisted as one of the top five in the ‘Best Student Contribution’ to a Small to Medium-sized Employer award!  

The award recognises the student who has exceeded expectations and genuinely made a significant impact to the small organisation as a whole. Natasha was nominated for her contribution to the UK Demographics Study that took place in 2020, the aim of which was to determine the demographic profile of Smith-Magenis syndrome across the UK.

Natasha impressed the SMS Foundation during her internship with how she approached the project, the methodologies she adopted drawing from existing skills and new knowledge gained, how she managed the time over the phases of the project, and the professional presentation of the results through the technical report, research poster, and online presentations.

Natasha impressed us during her Summer internship on the UK SMS Demographics project gaining positive feedback from our international community of clinicians, geneticists, researchers, and families. Natasha’s knowledge, experience, and adaptability to deliver innovative solutions naturally fits with our culture and vision.   I am delighted to welcome Natasha to our team as our part-time Research and Admin Assistant whilst she completes her degree in Biomedical Sciences at the University of Keele. 

Nigel Over, CEO

Shortlisted student nominations will be presented to the NUE Awards independent judging panel who will then review all of the candidates in the category. The winner will then be announced at the virtual Awards Ceremony on Thursday 25th February 2021, 3-5pm.

We all wish Natasha the best of luck with her nomination!

Share this post:

Facebook Twitter LinkedIn E-mail

Category: News

Previous Post: « Announcement of AGM
Next Post: December Newsletter snapshot of December newsletter»

Footer

Contact Us

Call: 0300 101 0034

Please note: This is an answerphone service that will alert us as soon as a message is left. A trustee will call you back as soon as possible – we aim to respond to messages within 24 hours.
  • E-mail
  • Facebook
  • Twitter

Quick Links

  • Press
  • Terms and Conditions
  • Data Protection & Privacy Policy
  • Disclaimer

Make a Donation

MAKE A DONATION

Regulated by

Fundraising Regulator logo

Site Footer

Cultivating talent finalist for breaking the mould SCA Terrific trustee award badge  NUE Awards - Shortlisted Nomination

Copyright © 2021 Smith-Magenis Syndrome (SMS) Foundation UK · Privacy Policy · SMS Disclaimer | Terms and Conditions