Vitamin L SAD light can help lift your mood, boost concentration and energy levels or treat the symptoms Seasonal Affective Disorder and winter blues
Feeling SAD?
Bright light, such as sunlight on a clear midsummer day, makes us feel positive, alert and energised naturally. However, many people don't get enough bright light during their day, particularly in autumn and winter. The short, dark days can trigger symptoms of 'winter blues', like lack of energy, wanting to sleep more and socialise less.
Light therapy is easy to fit in while you get on with something else.
Slim and lightweight, use Vitamin L SAD light at home or take it with you to improve well-being at work or when studying.Use Vitamin L SAD light every day for 30 minutes to recharge your batteries.
Vitamin L SAD light takes up hardly any room and can be used in portrait or landscape position.
Its slim design and relatively large screen means that Vitamin L lamp combines convenience with the performance you’d expect from a much larger light.Vitamin L is a registered trademark of Outside In (Cambridge) Limited t/a Lumie and is a reference to the mood-enhancing properties of light.
Specs
What people say
Vitamin L®
10,000 lux at 16 cm, cool white LEDs, rippled diffuser, portrait or landscape orientation. Game-changer!Compare wake-up lights
Functions
Functions
Rippled diffuser
Adjustable brightness and colour temperature
Day and Evening Modes
Light Source
Light Source
LED bulb, cool white, UV-free
LED - 5000K, cool white
LED - 3000K, warm white
UV-free
10,000 lux at 16 cm — 30 min
5000 lux at 30 cm — 30–60 min
2500 lux at 50 cm — 60–120 min
10,000 lux at 20 cm — 30 min
5000 lux at 32 cm — 30–60 min
2500 lux at 50 cm — 60–120 min
Touch Interface
Portrait or landscape use
Height
Height
28 cm (11 inches)
33 cm (13 inches)
Width
Width
20 cm (7.9 inches)
32.4 cm (12.6 inches)
Depth
Depth
8 cm (3.14 inches)
19.7 cm (7.8 inches)
Weight
Weight
0.830 kg (1.83 pounds)
2.22 kg (4.89 pounds)
Class IIa
Lumie is certified to ISO 13485 Medical Devices, QMS standard. Lights must pass rigorous safety tests and be supported by clinical research to meet the Medical Devices Directive EC93/42/EEC.