Fiica noastră are o afecțiune gravă | S08E04

Fiica noastră are o afecțiune gravă |  S08E04



Chiar acum, dacă accesați https://www.peltzshoes.com/Atticus, puteți obține o reducere de 15% la achiziție când introduceți codul „atticus” la finalizare. Când am decis să naștem în Malta, litoralul frumos și ancorarile izolate nu au fost motivațiile noastre principale. Am venit în Malta pentru că am vrut să fim pregătiți pentru cel mai rău caz. Având un sistem de sănătate reputat și engleza ca limbă principală, am simțit că Malta ar fi o alegere bună în cazul în care Isa ar avea probleme medicale.

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46 thoughts on “Fiica noastră are o afecțiune gravă | S08E04

  1. I really hope that Isabella will live a happy life with good health. My prayer is that her body will develop in a positive and normal way, without any negative effect.

  2. I dont pray much but I'm going to sit down tonight and have a long hard talk with whatever power is out there in the world. Wonderful people like you should get some protection from negative forces and I will try to force my will across the water to shower you with positivity. From Tampa , Florida I will wish and give my energy your way.

  3. I am very sorry to hear of the struggles you have been experiencing and what you are going to be going through. My daughter was born with multiple birth defects (Golden Har Syndrome plus extra anomalies). She was in the nicu for her first 6 weeks. She had her first surgery when she was two days old. Within those 6 weeks she had two more surgeries. When she was 6 months she reentered the hospital and was put on a ventilator for 11 weeks, and then had two Aortopexy's and when she was 10 months old the doctors found she a diaphragmatic hernia. During this time we learned she was the longest surviving child in the world. She is now 37. It is a long road so make time for yourselves, continue talking to each other because your baby needs you both. Stay positive. Love the channel

  4. sweetheart, you made a baby and she's a miracle ✨
    she's not faulty, she has toes, hands, she's breathing and she's beautiful…
    as she grows, she can make new cells from her food she consumes daily, via nutrients, these things can sway one way or the other or just stay the same..
    can I suggest looking into the lymphatic system as well because this is a massive part of interstitial waste (cells die and are replaced and this system does this job plus your immune system is intertwined in this system via the lymph nodes and inside the nodes are macrophages that deal with cell waste and is actually the immune system).. kidneys and bladder, gall bladder and appendix, testicles, ovaries are also connected to this system..
    rejuvenation takes place via the DNA's memory to make new cels for organs, blood, tissues, veins, arteries, skin, see we are comprised of cells and what we eat is our supermarket that stores nutrients for all cell making in the bone.. even bones are cells.. 
    anything ending itis is acid build up and can cause inflammation… to stop acid, is all you need to do is consume raw alkaline foods, these nutrients are called simple, like simple carbs, simple protein and simple fat (which if you look at a living plant that even gives us fruit need these 3 components within its structure and nutrients in the form of vitamins, minerals and trace minerals from the soil.. when heat is added, it changes the molecular structure causing it to go from simple to complex, people have heard of complex carbs, this means heat has altered the structure and harder to digest and can cause inflammation via the acid alkaline base.. we are natures science, even doctors are aware of acid alkaline.. the blood will always stay at a level of PH 7.4 and if it is too acidic, the body will use calcium from the plant structure to normalise this..

    giving Isabel the best chance of building herself up will determine on her diet too.. sunshine, clean air, rest and sleep.. 
    herbs are brilliant for healing too…
    you do need a degree or certificate to use medical science because they use medication but as a naturalist in nature science, all you need is the knowledge and understanding your body, what saliva is for, what hydrochloric acid is used for, things like that..
    I learnt about the lymphatic system and it saved my life, I too have a RARE issue, as I grew a web across my throat within my oesophagus and my oesophagus is 1/2 the size, instead of it being 30mm wide in diameter, mine is 15mm so the danger there is if I choke on foods hence finding out what saliva does, the medical profession want to balloon my oesophagus to widen it but this can cause adhesions from tearing and then I will be left with scar tissue, this could also make my oesophagus even smaller in diameter..plus if I drank carbonated fizzy drink, with the bubbles that make you burp, if this happened deep in my oesophagus, it could rupture and id be dead within minutes.. the last viewing I had, the web is gone ( its called web throat) but the diameter is the same, so it is probably something I had all my life.. I do find it hard to swallow certain things, I cant eat like capsicum, tomato, cucumber skins or apple, plum skins as they get stuck.
    but found when I worked on my lymphatic system, making new cells daily for whatever organ needs to be replaced, I know im giving my body its best chance to make 100% cells in a perfect state.
    the gentlemen I learnt from is Robert MORSE he can be found on utube under ROBERTMORSEND.. he explains this lymphatic system.. it saved my life..
    he is in Florida in America too.. he is on other platforms like rumble too.. he saved my life with this knowledge..
    I hope this may help, even to the point of knowing about this system..
    I will also continue to pray for you gorgeous baby and you two because you are special to me..
    if you did read this, I appreciate your time..
    much 💜 from Australia
    Levi-Daisy 🌸🙏💜✨

  5. Big hugs! Thanks for being so vulnerable and sharing I'm sure you are helping many as they go through their own struggles. Stay strong and embrace the journey. Again big hugs!

  6. I’m so sorry about beautiful Isa’s medical condition 😞 I wait for updates on her and I just have to say ‘thank you’ Jordan, for being so strong for your family. I am praying for all of you. What a blessing to have your parents there for one month, supporting your family and being a reminder to you that it’s okay to just stop sometimes, and cherish every single moment life has to offer. You have an AWESOME family and an AWESOME life. And to think….you have SO many people that, even though they may not be there physically for you, are there for you in spirit and ❤️ you guys so much. Cherish that little nugget 🥰

  7. Glad to see ya'll doing well. Seems like there's a lot of good news. It's tough being new parents even when there aren't surprises, so you're taking everything in stride very well.

    A rare disorder runs in my family too (spherocytosis), which impacted most of us in childhood. One thing we've learned was to always get a 2nd and 3rd opinion for each specialist. It's important to avoid having on person or even one team in a specialty become a single point of failure.

    Keep up the good work parenting, sailing, and film-making. There's no channel I look forward to watching more.

  8. Oh my goodness I can’t imagine. I’m am holding you both close in prayer. She’s beautiful and I am believing she is healed.

  9. What an honour for us to view that episode. Great family, so much love. You guys will all be absolutely fine. Our prayers are with you. 🇦🇺

  10. This is easy for me to say since it's not my child, but I'll share something a surgeon told us in the course of trying to figure medical issues. He said "Don't borrow trouble."

    Bottom line: try very hard not to worry about bad things that might be. It's hard, I know. But it's really best not to worry until you know.

  11. All the best to you and your family. Beautiful little one. My son was born with a Hemangioma on his face. It was gone by the time he turned 3 years old. My heart goes out to you Deseray. She is so lucky to have both of you and your families.

  12. Gracious and loving God, I pray for baby Issa that your healing and comforting presents will be with Jordan, Desseray, and Issa and that they will draw close to you and experience your compassion and love as you heal their precious baby. Calm their anxieties and give them your peace. I pray to you lord that you will intervene and sustain. Amen.

  13. Good to see that your baby is doing good … and grandparents spending time in Malta … and the upgraded repairs were successful … love being a viewer of your videos … will be waiting for the next one … thank you so much … see you next time …bye for now …

  14. What is you get the longer belt and a bigger pulley?

    The belt should have a bit more surface area touching since the circumference is bigger.

    Also with a bigger radius, the belt will have a longer lever arm and increase the torque on the alternator shaft.

  15. Heh – I've been doing the same paperwork run-around just trying to register a car from the UK – let alone a beautiful wee human being! You'll get there! Isabella will be in my thoughts. I hope to hear nothing but good news from here in.

  16. Our hearts go out for you guys. I totally hear what Des was saying about not knowing what’s normal and when you should be worried. I think your idler was great, super clean and easy installation. Be careful with the belt tension, the stud that it’s mounted on isn’t very big. Maybe keep that shorter belt around for awhile just in case! Cheers

  17. Hi guys. Having the baby diagnosed with a very complicated disorder at a very early age is quite not a thing for me to be worried. Cheer up, just let life takes its own development. Believe me, God does wonders and so does how he makes our life from a new born to what we are today. The first year of a new born is a miracle itself how our body takes its shape. See how god makes wonders and this happens to all newborns. The real challenge is also for both of you to raise the baby up in a boat life. Congratulations guys for the gift of life given to your baby.

  18. My friends,

    I love the journey you are on and wanted to share with you how inspiring what you are going through is. Many years ago (35+) I had the wonderful misfortune to have to raise a daughter as a divorced single parent who was a type 1 diabetic. The fear and fatigue of having a sick child is overwhelming. It is exhausting. But please know your hard work and love will make the difference. My daughter is 40 now. 5 years ago she was well enough to receive a kidney and pancreas transplant, and today (other than permanent vision impairments) is a beautiful and wonderful wife to an amazing son in law and no longer diabetic. And she is absolutely the funniest most stoic human being on the planet. If I could advise my younger self (I’m 63 now) about what to do that I didn’t do – I wouldn’t tell myself to do anything different. But your fears can bounce around in your head – know that almost always trusting your instincts and finding stillness and quiet (even for a minute on a crazy day) will keep you connected to the love/work at hand.

    A fan from the beginning.

    Dean in Tucson (a landlocked sailor).

  19. As a fresh grandpa, I can perfectly understand Desire's fears and feeling "not strong enough", but believe me Des, you are way stronger than you think and you will get through it like a Boss. As for the missing vein, I wouldn't rule out the possibility that they just weren't able to find it, but it is there. Wouldn't be the first time. Just hang on, the both of you, and everything will be fine.

  20. I have been watching all your video's in the last week…. What a inspiration you are to me! Congratulations with your beautifull daughter! I can imagine it is hard to hear that medical conditions are disturbing your happy feelings! Stay strong as you both are!

  21. As a parent of a disabled child (cerebral palsy), our first and now an adult, I would never change what occurred due to the growth I received as a person from raising a child with disabilities. The stress of not knowing is the toughest times, but with therapy and medical assistance, our son now has a fulfilling independent life, has his own daughter and is functioning just was well as anyone, except for pain and issues that must be indured due to the circumstances. My thoughts and prayers are with the three of you.

  22. God gives us hurdles to cross and you will cross over them with all of our prayers from your support team in the coming days. I too had little abnormal issues similar in nature and I did not know until years later of those human anomolies that make us all unique in our own personal way. Be strong and welcome to parenthood!

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