I have just got an oxygen monitor, the one that goes on your finger, and first few reads are upper 90's. I'm not sure if this is a good idea. What do you think? π€πππxx
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matthew55 I think they're a good idea. I have one and use it every now and then.
Sats in the upper 90s is excellent πππ It'd be great to measure them on waking, be that at 3am or after a full night's sleep (with and without your Z pills) ππβDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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Important to note: pulse oximeters were in the news over the weekend - they give higher (false) readings on darker skin tones, so should not be relied upon by some people. xxβDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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I've seen your photo π, but I am quite sure there are forum members with various skin tones, who ought to be aware of the issue. xxβDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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Originally posted by matthew55 View Post97 when I woke up
For comparison, with NIV on overnight, my oxygen level doesn't go above 95, and spends most of the night hovering between 92-94.
I'm happy for you π₯°π₯°βDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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Mary, an oximeter doesn't measure CO2 levels unfortunately. I think this can only be measured by blood sample from ear or wrist or somewhere?? I don't know if they are supplied by nhs, but are fairly cheap online xxDiagnosed July 2020, ALS bulbar onset. PEG and ventilator (mainly at night), and pretty poor speech, but legs still about functioning!
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