Hope2SleepGuide

Sleep Apnoea Forum Bringing Help + Support to the Patient

Welcome to our Forum - Feel Free to Introduce Yourself Here.

Welcome to the Hope2SleepGuide Forum, which is a service run by the Hope2Sleep Charity founded by Kath Hope with a marvellous team of trustees and volunteers. 

Kath herself has severe sleep apnoea and hypoventilation/hypercapnia, and has used CPAP for several years and is now on non-invasive ventilation.  Our trustees and volunteers are all either sufferers of sleep disordered breathing or clinicians/medics working in this field, and most importantly, we are all passionate in supporting (with empathy) others and raising awareness to help people live healthier and more energised lives.

 

Whilst we do not give medical advice, more often than not, with support, tips and knowledge, people can overcome any problems experienced with our therapy, and there is a whole page dedicated to this on the website http://www.hope2sleep.co.uk/tips-for-problems-sleeping-with-cpap-or...

 

Please come and join us, and don’t feel obligated to use your ‘real’ name if you prefer to remain anonymous as this is a public forum.  Don’t be shy in posting and sharing, as we’re all in this together and to help each other.

Best Wishes for good sleep!

Kath

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Hi Deborah,  since our last phone call, i would like to thank you for all the help you have given kev and my self in regards to the masks. he has tried the large and finds it more comfortable to wear. the room seems so quiet now that i keep checking on kev to make sure his machine is ok. we do get a bit of water in the bottom of the humidifier which i hope is normal.

we really can not thank you and your company enough.

much love from 2 very happy people

mel and kev x

You are most welcome, Mel!  Yes, the Simplus has a new diffuser in it ... mainly for the benefit of the partner :)  Is Kev finding any trouble with mask leak or anything like that?

Hi Deborah, no where near as much leaking as his other masks that he has tried. i would recommend this mask to other sleep apnea sufferers. for patients and partners. it is a very well made mask. x

Hi all

I'm a newly diagnosed OSA sufferer and, as of last Friday, a fellow hosehead(!).

It's all a bit new at the moment, though I seem to be coping with the CPAP machine and mask ok at the moment. I've even managed to maintain most of my beard, which has been with me for the past 15 years or so and which I was really loathe to lose. It was long overdue a good trim anyway! Today, for the first day in goodness knows how long, I've got through the day without feeling particularly tired - if I didn't understand the science I would say it's a miracle!

Looking forward to chatting and finding out more about this, frankly, rather odd world! 

Iwan

Pleased to hear you've managed to keep your beloved beard Iwan and even more pleased to hear you're already feeling the benefits of CPAP therapy!

Whilst many sleep apnoea sufferers at present feel rather isolated in their condition, they won't soon as more and more people get diagnosed.  Our condition is actually as common as asthma and diabetes, but at the moment only a very small proportion are diagnosed, and I'd go as far to say that we're the lucky ones



Iwan Davies said:

Hi all

I'm a newly diagnosed OSA sufferer and, as of last Friday, a fellow hosehead(!).

It's all a bit new at the moment, though I seem to be coping with the CPAP machine and mask ok at the moment. I've even managed to maintain most of my beard, which has been with me for the past 15 years or so and which I was really loathe to lose. It was long overdue a good trim anyway! Today, for the first day in goodness knows how long, I've got through the day without feeling particularly tired - if I didn't understand the science I would say it's a miracle!

Looking forward to chatting and finding out more about this, frankly, rather odd world! 

Iwan

Welcome Iwan, it becomes second nature to us, I look at it as an extra arm or leg and most of us will tell you that we can no longer sleep without it. It has saved my life. A lot of people get that sudden burst of energy, what sometimes happens is it tapers off for a while and after 3 - 6 months you start to feel like that everyday as your body starts to heal. Remember for most of us we have had this illness a long time. I'm sure if you read up on it a bit more from either posts on here or websites, the more you will learn and understand our illness and how interesting sleep can be  

Hi Terry , Kath and "the rest of the team" . .............me and the new machine , are going great guns . sorry I don't reply to much stuff on here lately . ive always got something on . so don't think im ignoring you or anything !!      kath <3

Good to hear your doing well Kath.

Great to hear Kathryn.  Onwards and upwards...

Kathryn Chapman, said:

Hi Terry , Kath and "the rest of the team" . .............me and the new machine , are going great guns . sorry I don't reply to much stuff on here lately . ive always got something on . so don't think im ignoring you or anything !!      kath <3

Hî there, I am new to this site and joined as I was looking for information about apnoea. I have been using a cpap for a year with some success. Went to see my consultant yesterday and asked to try the wisp and wore it for the first time last night and I have to say it s the best yet. It was very light and comfortable and I didn't try to rip it off in my sleep.

That's good to hear Terry, and I've actually been trialling the Wisp lately - no easy task for someone like me who is still a mouth breather and usually needs a full face mask.  I have to say that I was very impressed and feel that Respironics have had a great breakthrough with this mask and I especially think it will be great for people who are prone to nasal bridge problems.  I imagine the reason you didn't feel like ripping it off is because it's so small, light and feels so soft. It also seals well and I tried my best (for the trial) to cause a leak, which proved very difficult!  Just wish I could train myself not to open my mouth in my sleep, as I'm not a lover of chin straps!  Hope this mask continues to give you full success!

Terry Foxon said:

Hî there, I am new to this site and joined as I was looking for information about apnoea. I have been using a cpap for a year with some success. Went to see my consultant yesterday and asked to try the wisp and wore it for the first time last night and I have to say it s the best yet. It was very light and comfortable and I didn't try to rip it off in my sleep.

hi and welcome Terry

i too am now using the Wisp, as Kath has said i think Philips Respironics have he ally made a breakthrough with this one.

i thought the True blue was best until I tried the Wisp. My only comment to them would have been please can they make a Small, rather than Small/Medium size together as I think I am somewhere in between S/M & P, so I'm alternating them, The petite with the S/M but I'm finding air leaks into my eye on the S/M.

I guess most of their customers may be using the larger of the masks, even on the True Blue Mr Oko never kept a stock of the Petitle replacements. It wasn't a huge issue as he just calls Philips and tells them to send them out and the arrive next day.

I'm assuming from where you are from we possible see the same consultant :)

Ive been using CPAP now for about 18 mtgs and could have managed with out his or Kath's help. I wasn't an 'easy starter' lol

glad to hear that you are coping well  xx

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