Brazil SAD light is the largest Lumie lightbox providing bright light therapy. Just 30 minutes a day will help lift mood, boost concentration, restore natural energy and treat the symptoms of Seasonal Affective Disorder (SAD).
Need to recharge?
The short dark days can trigger Seasonal Affective Disorder (SAD) and 'winter blues'. Just as sunlight naturally makes you feel good, topping up with extra bright light in the winter months, or when you're stuck indoors, is proven to put you in a better mood and make you feel more awake. Using Brazil every day makes a big difference to symptoms of SAD such as tiredness, over-eating and a lack of energy and motivation.
Use Brazil SAD light for bright light therapy first thing to feel instantly energised and ready to tackle the day, or mid-afternoon to combat that midday fatigue.
Specs
Compare SAD & energy lights
Functions
Adjustable brightness and colour temperature
Day and Evening Modes
Ambient backlight
Light Source
Light Source
3 × PLL Broad spectrum bulb 36 W 840 4000 K, warm white, UV-free
LED - 5000K, cool white
LED - 3000K, warm white
UV-free
Treatment time
Treatment time
10,000 lux at 35 cm
Position Brazil at arm’s length (about 50 cm) and start with 30 minutes a day. If you need to, increase your exposure each day until you find a treatment time that works for you.
5,000 lux at 50 cm
2,500 lux at 80 cm
10,000 lux at 20 cm
In Day Mode, with the light at full brightness, you’re getting the maximum benefit so position Halo at arm’s length (approx. 50 cm) and start with 30 minutes.
5,000 lux at 32 cm — 30–60 min
2,500 lux at 50 cm — 60–120 min
Display
Touch Interface
Features
Features
Integral handle
Adjustable brightness and colour temperature
Day and Evening Modes
Ambient backlight
Height
Height
50 cm (19.7 inches)
33 cm (13 inches)
Width
Width
31 cm (12.2 inches)
32.4 cm (12.6 inches)
Depth
Depth
15 cm (5.9 inches)
19.7 cm (7.8 inches)
Weight
Weight
2.85 kg (6.28 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.
