Cystic Fibrosis Trust

Justyna's page

Justyna Zaskwara

Justyna Zaskwara

My Story

Hello and welcome to my page! ☺️

 

I'm Justyna, I'm 25 years old, and I cannot believe I'm about to do this!

 

I think I'm crazy, everyone else thinks I'm crazy, maybe I am crazy, but I'm going to be taking part in the TCS London Marathon 2025. Now there is a sentence I never thought I'd say out loud! 🤪

 

Cystic Fibrosis has been a huge part of my life for as long as I can remember. I was diagnosed with CF at 6 months old and it has been dominating ever since.

 

Working isn't always easy, exercising isn't always easy, and running a marathon with a lung condition especially isn't easy! Friends, family and colleagues have asked why I'm doing this - maybe I don't know either, but I know I want to do it!

 

Ohh and I might have forgotten to mention, but I am a complete newbie to this 26 mile journey!

 

But that being said, I wouldn't be me if I hadn't decided to embark on a crazy challenge! I'm just hoping that my lungs will work with me throughout this journey and not completely against me.

 

So far, they haven't exactly been on my side, and there have been a lot of ups and downs. I've struggled and I've cried, but I haven't given up... and I refuse to give up.

 

Despite everything, I'm very excited to be taking part, as I know it will be a wonderful event!

 

I'd be very grateful for your support in this fantastic event, as I'm doing it for such a great cause, which means a lot to me.

 

Keep Smiling, much of love J 💛 xx Saltycyster65_

PS. Thank you to the ones who inspired me to enter the LM25. 

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). We fund vital research, improve care, speak out and race towards effective treatments for all. We won't stop until everyone with cystic fibrosis can live without limits.

Cystic Fibrosis Trust is the UK's leading charity supporting people with cystic fibrosis (CF). 

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Since 1964, we've supported people with cystic fibrosis to live longer, healthier lives - and we won’t stop until everyone can live without limits imposed by CF.

Cystic Fibrosis Trust

Raising for:

Cystic Fibrosis Trust
1%

Funded

  • Target
    £2,500
  • Raised so far
    £25
  • Number of donors
    2

My Story

Hello and welcome to my page! ☺️

 

I'm Justyna, I'm 25 years old, and I cannot believe I'm about to do this!

 

I think I'm crazy, everyone else thinks I'm crazy, maybe I am crazy, but I'm going to be taking part in the TCS London Marathon 2025. Now there is a sentence I never thought I'd say out loud! 🤪

 

Cystic Fibrosis has been a huge part of my life for as long as I can remember. I was diagnosed with CF at 6 months old and it has been dominating ever since.

 

Working isn't always easy, exercising isn't always easy, and running a marathon with a lung condition especially isn't easy! Friends, family and colleagues have asked why I'm doing this - maybe I don't know either, but I know I want to do it!

 

Ohh and I might have forgotten to mention, but I am a complete newbie to this 26 mile journey!

 

But that being said, I wouldn't be me if I hadn't decided to embark on a crazy challenge! I'm just hoping that my lungs will work with me throughout this journey and not completely against me.

 

So far, they haven't exactly been on my side, and there have been a lot of ups and downs. I've struggled and I've cried, but I haven't given up... and I refuse to give up.

 

Despite everything, I'm very excited to be taking part, as I know it will be a wonderful event!

 

I'd be very grateful for your support in this fantastic event, as I'm doing it for such a great cause, which means a lot to me.

 

Keep Smiling, much of love J 💛 xx Saltycyster65_

PS. Thank you to the ones who inspired me to enter the LM25. 

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). We fund vital research, improve care, speak out and race towards effective treatments for all. We won't stop until everyone with cystic fibrosis can live without limits.

Cystic Fibrosis Trust is the UK's leading charity supporting people with cystic fibrosis (CF). 

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Since 1964, we've supported people with cystic fibrosis to live longer, healthier lives - and we won’t stop until everyone can live without limits imposed by CF.