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Cystic Fibrosis affects the cells that produce mucus, sweat, and digestive juices. It causes these fluids to become thick and sticky. They then plug up tubes, ducts, and passageways. Symptoms vary and can include cough, repeated lung infections, inability to gain weight, and fatty stools. *Dr Aboda*

God bless Tara!!!❤️🙏

I want to hug her

My grand daughter was just born with cf.

BRAVO a very very special Lady...and very elegant. Mrs.Mulroney is a shinning beacon of style, grace and determination for everyone. The children are well mannered well spoken and successful. merci and thank you Mila

Well Milan’s background is Serbian indeed we are part of commonwealth nations . My background is Ceylon Tamil In 2nd world war Irish nurse & indian doctors get married

Have always admired her. Sending heartfelt condolences.

NHL when I came to Canada I have no clue about ice hockey All my friends favorite team is Montreal Canadian I became Montreal Canadian fan . While I was living in Toronto I go to maple leaf hockey arena but I wear Montreal Canadian jersey

rest in hell and sandy ranando

Im a English speaking Canadian and French is known a frog's language Anglo-Saxon I hate this presentation thumbs down 👎

I am thankful to her for telling her experience. I wish the cheesy background music wasn't so loud, it's hard to hear her.

😂😂😂

Praying for you ❤

Très bien détaillé je le consulte tout le temps ❤❤❤❤❤❤❤

Can i suggest grow your channel?

Hi, Hope you are well. I hope visit your RUclips channel and your video making is very good. Your content ideas are very good. Thank you very much ♥

She's still with us! I saw her X account is very active as I type this November 2023.

You are the bravest woman ,I salute you

thank you for sharing your video, it helps a lot especially for a mom like me who lost a son perhaps due to this disease. My son was only two days old when suddenly he had difficulty in breathing, at that time he was already screened but the newborn screen result had yet to be released. It was seven months later when I and my husband had been informed that my son had cystic fibrosis and that he needed to be tested for further confirmation but he already passed after 2 days of given birth. At the time of his passing, we were really confused why my son suddenly suffer from difficulty in breathing and he did not take his feeding. We rushed him to the hospital but five minutes after we were catered in the emergency care, he was not able to get through. It was the saddest part of our lives, just remembering those time brought so much agony for me and my husband. We were blaming each other thinking we havent done well or that much for our son. We did not know that he had CF until such time his newborn screen result was released. We didnt know what is CF, so I had to google it and that's how I come across your video. It is painful to lost my son, It has been 2 years and the pain still lingers. But your video helps me understand and somehow accept why my Ronan could not make it. I hope you will not lose hope of fighting to live, you are blessed because your are able to make it 23 years of life. How i wish my Ronan had able to survive with it because I will really do whatever it takes just to make my son live..

Diagnosed In 1987

Has anyone else noticed a decline in mental health from those that took the vaccine.

I have CF and I can confirm through personal experience that there are a whole host of CF symptoms that were alleviated once a focused on my gut flora. I was already taking Trikafta and focusing on the things my doctor told me which made a huge difference. That difference was further improved when I began paying closer attention to my gut flora. Hope this helps other fellow patients.

great video, thank you

Please get checked for S. Aureus. Which causes abscesses/ pus which is dead white blood cells which are supposed to fight infection. if its ingested by inhaling or in contact with feces. My son swallowed meconium before he was born and had a lung infection and a hole in it and within a year had a blood infection. Heal your gut and please try colloidal silver because it penetrates mucous. Pus and mucous can be mistaken for just mucous. Plus their are other versions of the same thing just different levels of progression of the same problem.

I’ll show support to your family

🧚🏻‍♂️☯️🌹🌌🦅

I'm a healthy lucky one🤗

🧚🏻‍♂️☯️💒🗽🌎🦅🌌

Bless u

I have CF to and yes there is a lot about it, and just a couple of months ago I got a medication called “Trikafta“ and it truly changed my life. And it is scary, you don’t know ur future. Not knowing if u can go to college or have children if u don’t make it that far in life

Is there anyway to contact her?

:)!! Become a YT god > Promo-SM !!

Trina you are so beautiful and inspiring!!

Hello everyone and how can i personally recommend to you all Dr Ehimare herbal medicine on RUclips channel who cured me from fibrosis permanently with the use of his herbal medications cure treatment formula 💃💃

video anda sangat bagus dan mempunyai mesej yang luas terima kasih

Thank you for sharing and I’m hopeful that you are doing better with your new lungs

I only have to deal with bronchiectasis and it’s not great. God bless all your people.

hi Tara my name is Jon Ferguson I'm from Illinois I'm praying for you to get better my niece has cf she doing really well I'm going send you Alot of prays may God blessed you Jon Ferguson 💜💜💜❌❌🎈🎈🎈💗💓🌷🌹🌹

Tara, I have signed on to save a life here in Australia. A card we hold In our wallet. I have decided to surrender all of my organs if I shall die unexpectedly. My family knows all my wishes as they have also discussed with me. I have had friends growing up with CF in the church. One close friend who lived five years post transplant, was a wonderful thing. Bless you.

My fellow CFers: Can you move to California? I'm not kidding. I know that CA politics are messed up. However, it allowed me financial help for my extraordinarily expensive meds. I discovered GHPP, i.e., Genetically Handicapped Persons Program! It was like a gift from the Lord Jesus & I am so thankful to God!

A 6 ans elle va pouvoir en prendre.

I am so happy for you Lorna.

I am from India. I am 21 years old . Struggling with shortness of breath for more than one and half years. Still struggling. Sometimes I feel better, Sometimes I feel very bad , I am very tired, frequent fever and almost feeling fainted 😭 First diagnosed with Pneumonitis and then some ct's are taken. Some doctors tell scars(fibrotic bands) in the lungs but it's okay, You are alright. But my problems symptoms are same , not cured? I also had acid reflux and belch more than a year . I diagnosed with stomach ulcer. Some doctors didn't understand my pain. Still didn't got proper medication. Please help someone 😥, living with pain I hate the Nature which causes our lives so sad,

Tara dear it’s okay just enjoy your life no need to be worried 😟 I now it’s difficult I can do my best for you I can take you for nice doctor he can give you medicine for that and he can split that mucus which stuck in your chest dear that’s why you can’t breath well dear

How is this lovely lady now

It’s awful because even cost wise.. covering the medication would cost way less than all the hospital stays and potential lung transplant! Just WHY do this?!? And this is in Canada?? A lot of us Americans have been told plenty of times how healthcare is basically free/low cost compared to here. This video sounds like something out of the US! Goes to show you that Canada may not be so different than us? It sucks. It’s unethical..

How can I get approved?

Why cure you if they can just create the medicine that slowly treats you and keep making money off of your insurance, off of you.

Bless you, your family, and loved ones, thank you for sharing your story. I participated/volunteered in my first CF foundation great strides walk today, in West Virginia. I plan to get as involved as I can as time goes on. Last year I learned I was a carrier for CF, and no one in my family, paternal/maternal, was aware of being a carrier. I recently became a father of beautiful identical twin girls, both positive for CF. Born at 28 weeks 6 days. Strongest little girls. They have inspired me to do something greater with my time in this world. Very sadly, this past week I lost one of my girls at 68 days. Devestating. I am still figuring out how to come to terms with it. God has a plan for everyone, no matter how brief a life is, there is a purpose and change made in this world. Her sister is doing well as can be and I hope to take her home from the hospital very soon. She begins her enzymes this coming week. I am very blessed to have an emotionally supportive family surrounding me and we are getting through this tough time by coming together as one. May my sweet little girl rest in heaven and watch over her sister. Forever in my heart <3.

Thank you for sharing this ❤️