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Eyecare entrepreneur is awarded an MBE
Yorkshire businesswoman Sue Grant, the Co-Founder and Managing Director of The Body Doctor Ltd, has been awarded an MBE for Services to Entrepreneurship in the King’s Birthday Honours.A missed intraocular telescope – an opportunity to re-focus the evidence
Intraocular telescopes allow magnification of the image so that it would be projected into a larger area of the macula, this makes the central defect caused by dry age-related macular degeneration (AMD) smaller. The most common approach is a Galilean...Overcoming sight impairment for the Race Across the World!
RNIB’s Tricia travels the world and takes her message that "sight loss doesn’t stop you doing anything" to BBC One.Music and song inspire Freya to start speaking
Freya Reily, who is six years old from Tranent in East Lothian, is more than meets the eye. Freya, who was born very prematurely and has severe vision impairment, has been inspired by music and song to start speaking, something that her parents did not think was possible just a few short months ago.Strengthening eye care services in Botswana through the Botswana-Addenbrooke’s Abroad VISION 2020 LINK
The VISION 2020 LINK between Botswana and Addenbrooke’s Abroad has been running for 10 years. With support from the VISION 2020 LINKS Programme two-way exchange visits were undertaken leading to the formation of the first formal international partnership under Addenbrooke’s...100 years of insulin
*Joint first authors The centenary of the discovery of insulin is a time to celebrate one of the most significant scientific discoveries of the 20th century. Background Before 1923, Type 1 diabetes mellitus [T1DM] resulted in death from severe ketoacidosis...
PDI check Nintendo screening results
‘PDI check’ is a vision assessment game developed for the autostereoscopic upper screen on the Nintendo 3DS XL game console. Version 0.2.5 emphasises quick assessment of monocular acuity, stereoacuity and red-green colour deficiency. The purpose of this study was to...
Genetic analysis of choroideremia families
Choroideremia (CHM) is a rare X linked recessive chorioretinal dystrophy. Symptoms include nyctalopia and progressive peripheral field loss. Female carriers may have mild symptoms. Choroideremia is known to be caused by a mutation in the CHM gene. A multicentre human...
