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Ruby

Ruby
Joined Jan 2015
Bio

Diagnosed several years ago with sleep apnea and use my CPAP faithfully. Volunteer with several sleep issue groups and am a patient advocator.

Missouri

Ruby
Joined Jan 2015
Bio

Diagnosed several years ago with sleep apnea and use my CPAP faithfully. Volunteer with several sleep issue groups and am a patient advocator.

Missouri

Despite all the views one way or another on SA treatment (or non-treatment) for right now it comes down to this--CPAP is the most effective, least invasive and most affordable treatment there is. Not in all cases but most. Yes, we need to be educated on ALL options and even more on ALL ways that we can help ourselves by changing our lifestyles. How many people do that? Very few.

For most of us, oral appliances or implanted devises are not covered by insurance. Implants have a whole 'nother set of issues associated with them. That does not mean that we just accept the CPAP as the end all/be all but that it is what we have.

So what needs to be done? We need to advocate for better outcomes and therapies. Is that easy? Of course not. For one thing we are sleep deprived and face other health issues. When we don't, then I agree--laziness or apathy keeps the status quo. Speaking in generalities here--if you see a problem, do something about it. Join an advocacy group, write letters, make your voice heard.

Gremlin, I agree 100% that all the funding, research, education, etc. should be focusing on prevention and cures as well as better treatment options. But that's not where the money is. Research cannot happen without funding and funding goes towards CPAP more than anything because despite it all, that's what people are directed to. Should doctors be more proactive with this? Of course! Maybe we need to push them, I don't know.

Long-winded I know and lots to wade through and totally my opinion.