Cystic Fibrosis help find a cure

Since losing our beautiful baby sister Jennifer I have upped the game in fundraising for C.F and it's warrior family! Jennifer always done for others, she is the most caring, loving and genuine person I have ever met and we are so so lucky to of had her for 34 wonderful years. Jen is always positive and the life and soul of any party (as her many friends will tell you) She is a fantastic actress and her love of vintage fashion is outstanding. She really is the full package and testament to this is all the wonderful memories, anecdotes and funny quips that have been shared since she passed. She is and always will be loved by anyone who had the pleasure of meeting her. For many years we have fundraised for CF as it is a charity very close to our hearts. We hope to raise as much money as we can to donate to C.F and one day, hopefully sooner rather than later we can find a cure together. We are starting with a 13 mile CF North run and my husband Shaun will be the willing (victim) runner. Shaun has not ran since he chased the ice cream van at the age if 8 so you can imagine how we are all feeling about this! Good luck Shaun . Jennifer will be looking down on you with that cackle of a laugh and willing you on.  Please please help us to help them find a cure and donate whatever amount you can to help our future C.F warriors and their families not have to go through what we are going through now. We have a lot of fundraising ideas we are planning on carrying out this year including a 13 mile run, a summer Sunday fun day and other charity events which you are all more than welcome to join us and come together for this amazing cause. Please feel free to message me if you would like to be more involved, more the merrier Jen would say. She would be so so proud of all her lovely friends and family for coming together and joining the fight for C.F.  Breathe easy my beautiful girl xxx So we have smashed our first target so now we move onto T.Vs with freeview for the specialist C.F unit at Withenshaw where Jen was. She always said the Tv's were rubbish and also it would be amazing to raise funds for Alderhey c.f. ward so we could buy the children some PlayStations or Xboxes or whatever else they want. These kids spend at least 2 weeks at a time in Alderhey where they can't mix or play with each other and believe it or not but some of these children never get a visitor so sit alone in a little room for 2 weeks. Let's make their stay a bit better together. It would be amazing for us to rock up to the ward and put a smile on their faces. Do you want to join me in making a difference? I'm raising money in aid of Cystic Fibrosis Trust and every donation will help. Thank you in advance for your contribution to this cause that means so much to me. More information about Cystic Fibrosis Trust: The Cystic Fibrosis Trust is the only UK-wide charity dedicated to fighting for a life unlimited by cystic fibrosis (CF) for everyone affected by the condition. Since we started in 1964 we have dedicated ourselves to promoting excellence in research and clinical care, as well as providing practical support and advice to people with CF and their families. Our mission is to create a world where being born with CF no longer means a life-long struggle.