CF Mama's Wear Yellow Day Challenge
Kayley Dempsey
My Story
CF doesn't take a day off, so neither do we!
Cystic Fibrosis is a horrendous genetic disease with no cure . One of the many symptoms is thick sticky mucus in the lungs which makes it hard to breathe as well as harder to fight infection . Every day our bubs have to do physio to keep their lungs healthy and try to shift this mucus. This might be percussive physio (tapping/cupping on the chest in different positions) or it might be using breathing devices, or it might be exercise.
For one month, me and 70+ other CF mamas will join our kids in solidarity and commit to 20 minutes a day of exercise. I'm dealing with a nearly three year old and a three month old so it won't be easy! But no matter what life throws at them, our little ones will have to commit to their physiotherapy and other treatments for the rest of their lives. Please show some support if you can afford it, and thank you!
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Target
£400
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Raised so far
£535
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Number of donors
26
My Story
CF doesn't take a day off, so neither do we!
Cystic Fibrosis is a horrendous genetic disease with no cure . One of the many symptoms is thick sticky mucus in the lungs which makes it hard to breathe as well as harder to fight infection . Every day our bubs have to do physio to keep their lungs healthy and try to shift this mucus. This might be percussive physio (tapping/cupping on the chest in different positions) or it might be using breathing devices, or it might be exercise.
For one month, me and 70+ other CF mamas will join our kids in solidarity and commit to 20 minutes a day of exercise. I'm dealing with a nearly three year old and a three month old so it won't be easy! But no matter what life throws at them, our little ones will have to commit to their physiotherapy and other treatments for the rest of their lives. Please show some support if you can afford it, and thank you!
