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General Discussion on any topic relating to CPAP and/or Sleep Apnea.
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LowOnJuice
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Joined: Mon Aug 16, 2010 9:41 pm
Location: Wisconsin
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New to this Forum

Post by LowOnJuice » Thu Aug 19, 2010 9:47 am

Howdy, I've been posting at the Sleep Apnea Support Forum for a few months now, and I found you guys while in my endless search for more Sleep Apnea information. I was diagnosed in September of 09', and I got my machine in October of the same year. I'm 22 and it's amazing how much a CPAP improves your quality of life, how it changes your disposition and overall mood about things, it's just an unbelievable machine.

Despite all of this, I can't seem to make people understand how serious this was in my life, and how much it actually changed me and the way I live. How do you get the people around you and in your life to understand?

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Emilia
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Joined: Mon Jul 12, 2010 8:56 am
Location: Florida, USA

Re: New to this Forum

Post by Emilia » Thu Aug 19, 2010 9:56 am

I know it can be frustrating, but, really, why do they need to understand something about which they have no knowledge? I have no idea what it is like to be a diabetic, and if my diabetic friends tell me what it is like, I still can't empathize since I don't have it! I can offer support, but I'll never know what it is like. It is your OSA, and even that is different than mine or others who have it. It manifests differently in all of us to degrees. So, while I may have low-end moderate hypopnea syndrome, someone else may have severe OSA, but we both use the same equipment to treat it. I still have no idea what it is like to have severe OSA!

Ebrace your therapy for yourself and enjoy your new found energy and rest. Don't worry about others......
Last edited by Emilia on Thu Aug 19, 2010 10:07 am, edited 1 time in total.
Yes, that blue eyed beauty is my cat! He is a seal point, bi-color Ragdoll. I adopted him in '08 from folks who could no longer care for him. He is a joy and makes me smile each and every day.

nanwilson
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Joined: Tue Apr 13, 2010 10:35 am
Location: Southern Alberta

Re: New to this Forum

Post by nanwilson » Thu Aug 19, 2010 10:07 am

Hi
What Emilia said...and double ditto! Don't stress yourself out about what others think, simply enjoy your newfound energy and strength.
Cheers
Nan
Started cpap in 2010.. still at it with great results.

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elena88
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Location: california

Re: New to this Forum

Post by elena88 » Thu Aug 19, 2010 11:04 am

The first person who saw my machine was my neighbor, I had not told her anything about it.

She peeked at it, and said" Oh, so this is the machine that keeps you alive?"

I was shocked she put it that way, but she had a young thin fella friend who had one for years, so she knew..


You can educatate the people around you, it is possible, but they have to WANT to be interested..


otherwise, its just something they dont want to hear about, and if they dont hear about it, maybe THEY wont get it..

( its that "not me" syndrome)

_________________
Mask: Swift™ FX Nasal Pillow CPAP Mask with Headgear
Humidifier: S9™ Series H5i™ Heated Humidifier with Climate Control
Additional Comments: sleep study: slept 66 min in stage 2 AHI 43.3 had 86 spontaneous arousals I changed pressure from 11 to 4cm now no apap tummy sleeping solved apnea