Beth's Cystic Fibrosis Story | Nuffield Health

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  • čas přidán 18. 12. 2016
  • The 16-year-old isn’t taking the life-limiting condition lying down. She’s fighting her CF with a fitness programme designed to improve her quality of life. Find out more at bit.ly/2gITnyj
    For five years Nuffield Health have been running a cystic fibrosis programme in partnership with Great Ormond Street Hospital enabling over 100 children and teenagers to benefit from the exercise-based initiative.
    The programme provides free Nuffield Health gym memberships and personal training sessions to both the young patient and their parent or carer, with the aim of slowing the rate of decline and reducing the amount of time children and teenagers have to stay in hospital for treatment.

Komentáře • 74

  • @IrishAutumn
    @IrishAutumn Před 5 lety +17

    What's wrong with people disliking important videos like this? 😒

  • @charlottebruce979
    @charlottebruce979 Před 4 lety +18

    This is why self isolating is so important at the moment.

    • @thetruthstrangerthanfictio954
      @thetruthstrangerthanfictio954 Před 2 lety

      Important eh? That same isolation is killing people. Unless you trust the almighty Saint Fauci word for word, then the real science suggests lockdowns do nothing to stop the virus and weaken people's immune systems by making them depressed. In Fauci we trust!

  • @addisonstine1585
    @addisonstine1585 Před 4 lety +42

    Haha I have cf and I’m watching this while I’m doing my nebulizer treatment. Keep it up, it’ll never be easy but you can do it! I’m I’m my teens and have never been hospitalized!

    • @addisonstine1585
      @addisonstine1585 Před 4 lety +4

      ItsGpx Still going strong! I recently received the new Trikafta treatment, and it is totally a life changer! I am hoping to start cutting back on medicines gradually! The Lord has been so good to me and it feels amazing that He has used me though my weaknesses.

    • @farhafarook1142
      @farhafarook1142 Před 3 lety +2

      Hope everything is going good for you!

    • @El-Niil
      @El-Niil Před 2 lety +1

      How are you doing now

    • @kellyray2302
      @kellyray2302 Před 2 lety +2

      I have been hospitalised and I am doing my nebulizer whilst watching this

  • @chrismorris6198
    @chrismorris6198 Před 4 lety +18

    My friend just lost his daughter to this condition ... She was only 10 years old 😓... Please pray we find a cure for this condition , so no parent goes threw what my friend is going threw right now ever again 🙏🏾🙌🏾

    • @charlottebruce979
      @charlottebruce979 Před 4 lety +2

      Praying daily. I'm so terribly sorry for you and your friends loss.

    • @Youre_Right
      @Youre_Right Před 2 lety

      Unfortunately it’s a genetic issue and there’s so much taboo around genetic engineering. Some Christians just view it as playing God. They’ve made some great advances in treatments. There is one form of CF that is almost curable as they can make the faulty gene stop reproducing the faulty gene and produce a healthy one.

    • @kristiankolev8435
      @kristiankolev8435 Před 2 lety

      @@Youre_Right what is that form please tell me I am 15 year old boy with cf

    • @george_2172
      @george_2172 Před rokem

      I’m sorry to hear that, May she Rest In Peace 🙏

  • @mollymacri
    @mollymacri Před 3 lety +5

    I was born with CF. You’re a fighter, keep up the good work:) Im happy I was born an “athletic” person, I can keep my lungs healthy

  • @george_2172
    @george_2172 Před rokem +2

    I hope she’s doing good still, I can’t imagine what’s it like to go through this but she’s very brave 🙏

  • @JihadAlAnsari
    @JihadAlAnsari Před 5 lety +34

    Excellent, I love medical science because how it can improve peoples lives! Especially if it was not their fault to begin with :)

  • @CFlifestyleFoundation
    @CFlifestyleFoundation Před rokem +3

    Thank you for sharing this inspirational story!

  • @bradskeels9649
    @bradskeels9649 Před 4 lety +6

    God bless her I hope she is doing well 💙

  • @stephenkeegan5625
    @stephenkeegan5625 Před 5 lety +22

    that's great for her well done guys 💜

  • @Kez_abi
    @Kez_abi Před 4 lety +1

    Ide happily have her personal trainer 😅🙈 shes pretty too
    Anyone else thinks she looks older than she is?
    What amazing work GOSH is doing

  • @carlosb1
    @carlosb1 Před 4 lety +3

    I love boxing. Boxing is a great sport and exercise for your lungs ;) Good job!! You will be ok young lady keep it up!

  • @dkdkdkdk0037
    @dkdkdkdk0037 Před 4 lety +4

    I have cysic fibrosis too but my pancreas works and i dont cough at all thanks to the doctors and the medication i hope every one has acces to the new symkevi medication for cystic fybrosis

    • @laylasleiman1981
      @laylasleiman1981 Před 3 lety

      It so obvious that patients with herpes virus are being enslaved to the antiviral drugs that is being prescribed by medical doctors to help suppress and not to cure them completely from the virus they have been battling with "a society that keeps cure a secret so they can continue to sell medication for huge profits is not a real society but a huge mental asylum" I suffered from herpes for three years using medical treatment hoping that one day God will do wonders In my life, a stranger I met at the park felt sorry when she saw the blisters on my face she immediately introduced me to herbalist oduntun from west africa I was convinced that he can cure me completely from the virus so I decided to go into natural remedy with herbalist oduntun.
      I contacted him on his instagram page @herbalist_oduntun we discussed and he explained everything to me how I will get the herbal medication, the prescription and food diets i will be on while taking the herbal medicine, I was on medication for 21 days following the these rules without eating meat or any diary product. (i'm on plant base🌿 )
      I give thanks to God almighty for leading me to the stranger that introduced me to this genuine herbal doctor I'm really grateful🙏🏼 for more information on how to reach him here is his email address: herbalistoduntun@gmail.com or what'sApp number: +2349039463501 Stay Safe Good luck.

    • @dkdkdkdk0037
      @dkdkdkdk0037 Před 3 lety +2

      @@laylasleiman1981 dont care

    • @laylasleiman1981
      @laylasleiman1981 Před 3 lety

      @@dkdkdkdk0037 Your Choice Not Mine 🙋

    • @dkdkdkdk0037
      @dkdkdkdk0037 Před 3 lety +2

      @@laylasleiman1981 theres no cure for cystic fibrosis they is new medication coming out for it just cause u belive everything you see on the internet

    • @dkdkdkdk0037
      @dkdkdkdk0037 Před 3 lety +2

      @@laylasleiman1981 just say to the my doctors 'oh i saw this comment saying doctors just give medicen for no reason so im gonna go'

  • @random_trap_boy_things191
    @random_trap_boy_things191 Před 5 lety +10

    i have cistic fribrosis and more like azma and more my life sucks

    • @sendhelp4402
      @sendhelp4402 Před 4 lety +4

      Jennifer Workman Sorry to hear that, but don’t pity yourself! Live your life as best as you can!

    • @urospeteh2637
      @urospeteh2637 Před 3 lety +1

      My life sucks too. I have respiratory reflux, also known as lpr.

  • @GameOver-mr7yc
    @GameOver-mr7yc Před 3 lety +1

    My weak physique due to illness

  • @Reinguko
    @Reinguko Před 5 lety +6

    Can a transplant of gut flora help this condition?

    • @nicoleabbott5115
      @nicoleabbott5115 Před 5 lety +6

      No. CF is caused by a mutation in a gene that allows the flow of salt through organs. This causes thick mucus like secretions that result in a higher chance of Infections, lung failure, and more. CF is fatal and there is no cure.

    • @Hedgeflexlfz
      @Hedgeflexlfz Před 4 lety +2

      No, it's genetic. Besides, that wouldn't do anything.

  • @kingdre1275
    @kingdre1275 Před 4 lety +2

    I have it to and it’s hard

    • @urospeteh2637
      @urospeteh2637 Před 3 lety +1

      May i ask what is your main symptom? My dyspnea is 24/7.

    • @thevilkids
      @thevilkids Před 3 lety +2

      @@urospeteh2637 how are you now? Do you use oxygen pumps?

    • @laylasleiman1981
      @laylasleiman1981 Před 3 lety

      It so obvious that patients with herpes virus are being enslaved to the antiviral drugs that is being prescribed by medical doctors to help suppress and not to cure them completely from the virus they have been battling with "a society that keeps cure a secret so they can continue to sell medication for huge profits is not a real society but a huge mental asylum" I suffered from herpes for three years using medical treatment hoping that one day God will do wonders In my life, a stranger I met at the park felt sorry when she saw the blisters on my face she immediately introduced me to herbalist oduntun from west africa I was convinced that he can cure me completely from the virus so I decided to go into natural remedy with herbalist oduntun.
      I contacted him on his instagram page @herbalist_oduntun we discussed and he explained everything to me how I will get the herbal medication, the prescription and food diets i will be on while taking the herbal medicine, I was on medication for 21 days following the these rules without eating meat or any diary product. (i'm on plant base🌿 )
      I give thanks to God almighty for leading me to the stranger that introduced me to this genuine herbal doctor I'm really grateful🙏🏼 for more information on how to reach him here is his email address: herbalistoduntun@gmail.com or what'sApp number: +2349039463501 Stay Safe Good luck.

    • @laylasleiman1981
      @laylasleiman1981 Před 3 lety +1

      @@urospeteh2637 It so obvious that patients with herpes virus are being enslaved to the antiviral drugs that is being prescribed by medical doctors to help suppress and not to cure them completely from the virus they have been battling with "a society that keeps cure a secret so they can continue to sell medication for huge profits is not a real society but a huge mental asylum" I suffered from herpes for three years using medical treatment hoping that one day God will do wonders In my life, a stranger I met at the park felt sorry when she saw the blisters on my face she immediately introduced me to herbalist oduntun from west africa I was convinced that he can cure me completely from the virus so I decided to go into natural remedy with herbalist oduntun.
      I contacted him on his instagram page @herbalist_oduntun we discussed and he explained everything to me how I will get the herbal medication, the prescription and food diets i will be on while taking the herbal medicine, I was on medication for 21 days following the these rules without eating meat or any diary product. (i'm on plant base🌿 )
      I give thanks to God almighty for leading me to the stranger that introduced me to this genuine herbal doctor I'm really grateful🙏🏼 for more information on how to reach him here is his email address: herbalistoduntun@gmail.com or what'sApp number: +2349039463501 Stay Safe Good luck.

    • @urospeteh2637
      @urospeteh2637 Před 3 lety +1

      @@thevilkids Hi, sorry, i havent seen your reply. No, no pumps. I don't have CF, but a secondary lung disease due to a post viral autonomic nervous system damage. You can read about it. Esophageal aperistalsis-dyspnea.

  • @wataahero5741
    @wataahero5741 Před 3 lety +2

    if you know you have the gene why not adopt i dont get it

    • @harrytheman1000
      @harrytheman1000 Před 3 lety +3

      Because even with CF it’s still worth having a life in the first place.

  • @carterhill7890
    @carterhill7890 Před 3 lety +2

    Badminton racket

  • @michael_pow
    @michael_pow Před 4 lety +4

    Hey that’s me! @mbpt_coaching

  • @toptierindustries3498
    @toptierindustries3498 Před 5 lety +1

    I also have cf and a very similar story to you. Check out my instagram and youtube

  • @joebastianich3410
    @joebastianich3410 Před 3 lety +1

    Box woman

  • @eidygra5350
    @eidygra5350 Před 3 lety +1

    It's not like that for everyone

    • @fontzy6010
      @fontzy6010 Před 3 lety

      Yes it id

    • @eidygra5350
      @eidygra5350 Před 3 lety

      @@fontzy6010 how would you know? Are you everyone?

    • @fontzy6010
      @fontzy6010 Před 3 lety

      @@eidygra5350 everyone with cf has the same thing

    • @eidygra5350
      @eidygra5350 Před 3 lety +1

      @@fontzy6010 nope
      Overall it's pretty similar but it varies from case to case
      I honestly don't even remember what the video is about but I can tell you that there can be a huge difference on how CF effects one patient or another
      It's mostly about which mutation you have
      Every mutation is different

    • @fontzy6010
      @fontzy6010 Před 3 lety

      Oh okay sorry. It’s just because I have cf and I do the same stuff as her

  • @mazenammarvlogs8925
    @mazenammarvlogs8925 Před 2 lety +1

    shes litteraly capping soooooooo hard rn she doesnt have cystic fibrosis... i researched about it in my 9th grade biology class today and she doesn't show any symptoms....

    • @xrachybabex1
      @xrachybabex1 Před 2 lety

      What a horrible comment, I have this and you wouldn't think it at all .

    • @adrigovea8
      @adrigovea8 Před 2 lety

      @@xrachybabex1 when were you diagnosed? What are your symptoms? I just started researching this as I think my son may have this. He never had the new born blood screening.

  • @jonsmith7220
    @jonsmith7220 Před 3 lety +2

    feeling there is something unhealthy between the trainer and her.. the way he talks sounds more like a bf

    • @len2489
      @len2489 Před 2 lety +1

      Because he doesn't sound professional like most personal trainers would?? Definitely doesn't sound like her bf lmao