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Low oxygen levels - what is normal?

My son has recently had a sleep study revealing his o2 levels drop to 73% at night which is now leading to intervention by way of a mask and oxygen and is looking as though it might prevent much needed scoliosis surgery.
My cousin in NZ also has a son with CP who also has similar night time o2 levels but the drs there have decided that is 'normal' for him and there is no intervention.
Is this a common condition amongst (young) adults with CP? How is it managed for you? Any advice/thoughts?
My cousin in NZ also has a son with CP who also has similar night time o2 levels but the drs there have decided that is 'normal' for him and there is no intervention.
Is this a common condition amongst (young) adults with CP? How is it managed for you? Any advice/thoughts?
Replies
I am an adult with CP so the information I am about to share with you might not help answer you question, but here goes nothing.
About 2 years ago, I began having trouble breathing at night after going to bed. I would gasp for air all night hardly sleeping more than a few minutes at a time. My breathing could be compared to how a goldfish would appear to breath if it was removed, even briefly, from its tank. In daytime, initially, my breathing was normal.
About two weeks later, I noticed that I began wheezing at night and was somewhat congested. I thought at first that I was developing a cold but during the day everything seemed normal. Unfortunately, that was not the case and days later I ended up at the hospital where I was diagnosed with allergy-induced asthma. I was given emergency treatment and put on daily inhalers. (I had not had any allergies/asthma issues prior to moving).
In addition, they determined that I had a problem with my thyroid level. It was too low. Once I was put on medication and the level was normalized, everything returned to normal.
Now, my doctor checks my thyroid level through periodic blood work. So far, the level remain stable and all has been well. Perhaps, if these things are checked, your son's condition will get better and he can have the other surgery he needs. Good luck, J
PS I'm not a doctor or an expert, I can only comment on my experience. Best to discuss with your child's respiratory docs.