NEW POST up on my blog https://eloiselaughlearnnurse.home.blog/ . . Each Tuesday I intend to post about a different condition I come into contact with the most on the ward I work on. Just to give some information for those interested. . . "I never knew anyone with Cystic Fibrosis growing up, so I didn't know much about it until I starting my training. The ward I work on.. we see it a lot. It is something I have a real interest in at work and I feel is something that should have much more awareness out there than it does currently. I'm sure most people have heard of it(I hope anyway) or some may even know someone who has it. Most people will know it to be to do with the lungs. But it's much more than that" . . For the rest of the post go at my blog 😁. . . For more posts follow ma insta 🤷♀️💁🏼♀️ . . For more info on CF visit @cftrustuk 💛. . . #nursingblog#nurselife#nurseblogger#childrens nurse #nurselife#bloglife#blogger#blog#newtothisblogthing#follow#cysticfibrosis#cf ,#,newblogpost
- Gemeinsam Mukoviszidose besiegen - Mukoviszidose ist derzeit unheilbar, aber Organisationen wie Mukoviszidose e.V. arbeiten immerzu daran, die Lebensqualitäten und die Lebensdauer der Leute zu verbessern. Durch Forschung, aber auch durch direkte Patientenhilfe. Alleine in Deutschland sind ca 8000 Menschen betroffen. Schon kleine Geldbeträge können den Patienten helfen und die Forschung vorantreiben. Deswegen lasst uns spenden. Postet bis zum 01.06.2019 ein Foto von eurem Exemplar von "Solange wir atmen" (egal ob Ebook oder Taschenbuch) in eurem Feed. Verlinkt mich darauf oder nutzt den Hashtag #solangewiratmen und ich spende dafür 1€ an Mukoviszidose e.V. (Infos zu der Arbeit finder ihr auf www.muko.info) . . . #angelwingverlag#cf#mukoviszidose#bookstagram#instagram#spenden#krankheit#lasstunsspenden#instabook#jugendbuch#cysticfibrosis
👶🏻🔬 Infertility as per the American Society for Reproductive Medicine (ASRM) Tue, 23.April.2019 #medicine#doctor#ivf#pgd#fertility#infertility#pregnant#pregnancy#health#wellness#asrm#genetics#reproductivemedicine#cysticfibrosis#downsyndrome ------------------------------------------------------------------------------------------------------------- العقم (من موقع الجمعية الأمريكية لطب الإنجاب) 🔬 تعريف العقم: عدم القدرة على الحمل خلال سنة من المحاولة بدون إستخدام أي موانع.. أو عدم القدرة على الحمل خلال ٦ أشهر إذا كان عمر المرأة ٣٥ وأكثر 🔬 ١٠ لي ١٥% من الأزواج في العالم يعانون من العقم 🔬 ثلث مشاكل العقم بسبب الرجل، الثلث بسبب المرأة والثلث الآخر بسبب عوامل مشتركة 👩🏻👨🏻 🔬 أسباب العقم: العمر.. مشاكل في التبويض (بسبب أمراض مثل تكيس المبايض، الغدة الدرقية، الهرمونات).. تشوهات في قناة فالوب، الرحم.. العنصر الذكوري (تشوه/قلة/عدم تكون الحيوانات المنوية، السمنة، التدخين، السكري، التليف الكيسي cystic fibrosis، أدوية مثل الماريوانا).. طفرات جينية 🧬 🔬 من نراجع إذا عندنا مشاكل في الحمل/العقم؟ - للبنات: طبيب/طبيبة نساء وولادة (تخصص عقم) - للشباب: طبيب/طبيبة مسالك بولية (تخصص عقم) 🔬 هل ممكن يكون العقم بسبب طفرات في الجينات أو الكروموسومات؟ 🧬 إي ممكن.. مثال: 👨🏻⚕️ الشباب: متلازمة كلاينفلتر، متلازمة داون، طفرات جينية على الكروموسوم Y، عدم تكون
Did you know...? People with cystic fibrosis taste salty. CF affects epithelial cells in the skin's sweat glands. Kids with CF may have a salty "frosting" on their skin or taste "salty" when their parents kiss them. They also may lose abnormally large amounts of body salt when they sweat on hot days. #cfawareness#cysticfibrosisawareness#salt#salty#cysticfibrosis
Get ready for Saturday, April 27th! The villains are bringing back the 65 Roses show benefiting the @cf_foundation on behalf of @thegarbergforce! Since 2013, LHTG has earned over $20,000 to help the 70,000 individuals fighting this disease find a cure. LHHSGUILD.COM #curecf#65roses#cysticfibrosis#lhtgfamily
Haven’t play in a while , i was inspired by @claire.wineland Story about her life and having CF (CysticFibrosis) . I have to say to everyone with cystic fibrosis, you are the strongest people out there . You smile through it all . You will forever be heroes. #livelife#cysticfibrosis#endcf#fivefeetapart#dontgiveuponme#clairewineland - Don’t give up on me by @andygrammer
Help promote CF Awareness and wear The Garberg Force or LHTG 65 Roses shirt on Thursday! Post your photo and tag us! Take part in annual group photos too: LHHS: Meet at the tables by the theater right at break! UCLA: Meet in front of Royce Hall at 6:30 PM! OCSA: Check with OCSA team leaders, Larkin Ten Elshof and Landon Wouters. EDHS: Check with EDHS team leaders, Meghan Broadwater, Harrison & Kendall Bangert #cysticfibrosis#cysticfibrosisawareness#curecf
Working out for the first time in 15 months. Why? Because with each of my babies, I have had crazy amounts of pain and issues with my back and hips that I wasn’t able to workout! It was SO hard each time. I always wanted to be the fit preggo momma but I never could! I was thinking today that truly just starting can sometimes be the hardest step. As I was finishing an audio book while running, something he said was “Future success is dependent on what you do today.” Those little, “insignificant” things today, DO make a difference! What is one thing you can do today to start?!?
So two years ago today I lost a brother/best friend. Everyone experiences passing of a loved one differently. I have been to many funerals the last couple years some older some younger and have watched how people go through with it. I may be different with passings an look at it differently. The person who passed definitely doesn't want to see people sad. So I look at it as an opportunity and as an experience. I wish nobody had to go through the death of someone but it’s life and sometimes life can be great and sometimes it gives you struggles. Either way look at it as the times you were able to have with that person sometimes good sometimes bad . Just remember they will always be looking after you, watching over you, and even though they aren't there physically they're there. #cysticfibrosis#bestrong#grow#cfwarrior#findacure#bestfriend#brother#untilwemeetagain
I made a promise four years ago and saw it through today. I am proud to say that my beautiful mane raised $2000 for the Cystic Fibrosis Foundation and will soon be made into a wig by the Wigs for Kids foundation as well. The flow will return again one day. #sigep#cysticfibrosis#wigsforkids
Claire always "Lived Proudly". What is your intent? Head to www.myintent.org to choose your word and style, and receive a special 33% off your purchase with the promo code "CLAIRE". Our partnership with @myintent will donate back 33% of every purchase to Claires Place Foundation.
I have to #bereal with you all... . Ever since I announced I will shave all my hair off if my #andreasangels team raises $50,000 by the end of the year for the @cf_foundation I have been feeling quite terrified! . Yes, terrified of going bald because, let’s face it, I’m vain and I like how I look with hair! . Yet, I’m more terrified about not raising the $50k because I know me...I will feel like a failure! I know, I know, I’m not a failure but I’ll still feel like one. . However, I’m mostly terrified about not funding the science that has saved my daughter’s life and the lives of many CFers, plus the lives they will continue to save, plus provide ALL #cfers with wonder-drugs, and mostly until they find a cure for all #fibros and #cysters worldwide! . I NEED YOU!!!! . Join our fight. Register to raise funds on behalf of @_arider here: http://fightcf.cff.org/goto/andreasangels (link in bio) . Or make a donation clicking on the same link, then PLEASE ask family and friends to match your donation. . Thank you, thank you, thank you!!! . #cf#cysticfibrosis#cff#cysticfibrosisfoundation#cfirl
#yellowheartsquad it’s important to spend time around people who make you laugh, smile, and feel good overall. Today, I had lunch with my good friend @ziplu on the #disney backlot. It was so great to catch up over good food. I left feeling rejuvenated and inspired. Jamie and I have been friends for 15 years. She works with the group of people responsible for so much of the incredible work that Disney does in the world, including the support with my children’s book, “the Spider Who Never Gave Up!” In the moments that I feel lowest, it’s people like her that lift me back up and remind me why I’m fighting. #fightcf#cysticfibrosis#transplant#donatelife#gratitude#hope
Sixty-Five Long Sleeve Shirt Cystic Fibrosis themed long sleeved shirt, part of the "Just Breathe" collection Super soft Mens/Unisex Gildan 100% ringspun cotton. For sizing guide visit site.(Link in Bio) $2 of every purchase will be donated to #cysticfibrosis until CF stands for #curefound . . . . . . . . . . .
Happy Earth Day!! 🌎🌏🌍 just a sample of the #cf medical type waste produced daily / weekly / monthly I try to do my part and separate what I can put in the recycle bin...but who knows if that ever gets recycled? This doesn't even account for: • 10 - 12 glucose test strips ------> EVERY DAY • lancets • insulin pump infusion sets • infusion set packaging • carbon footprint to get all this stuff delivered by courier thank you #cysticfibrosis science, sorry #planetearth#cfirl#cfrd
In ✌️days, @fit4mom_smyrna_vinings is hosting #bringyourkidtoworkout day to raise money for Team James Alexander, benefiting the @cffgeorgiachapter. Join us on Wednesday, 4/24 at 9:15am at @cumberlandmall to make a difference in these kids’ lives - your donations are tax refundable and 90% funds #medical research that’s truly changing lives. #mondaymotivation: Pictured here is a member of our village, @alexia_sophia, her son James and her husband @samual916, with another family you can follow at @drivingmissdesi who also battle #cysticfibrosis. The kids are wearing purple shirts because this helps identify who has CF. Those battling this disease must stay 6ft apart from one another to avoid cross contamination. Meaning, if James is carrying a bacteria, and came less than 6ft from another person with CF, just by being within that proximity without a mask covering his face, hand gloves - precautions we need to take when we’re around each other, he could infect the other person with CF with bacteria they probably didn’t have. Through your donations, families like these hope to not only enjoy more days with their children and watch their children grow well into adulthood, but hopefully one day their children get to interact in-person with others battling the same disease without feeling so isolated. #untilitsdone#curecf#cfirl#giveback#socialgood#monday#mondaymood#hope#raredisease#momlife#dadlife#toddlerlife#parenthood#atlanta#smyrna#vinings#togetherforjames
This is what I do 3/4 times a day, everyday. For about 20/40 minutes each session. Everyone with Cystic Fibrosis has a different routine and different machines, I still sometimes ask what other people use for there airway clearance! • • • I would show you how we have to get the mucus out of my lungs, but I don’t want you guys to see my tomato face!! And what’s inside the bowl later... • • • #cysticfibrosis#everyday#lifewithcysticfibrosis#cf#airwayclearence
I am so overwhelmed by the amount of people who have donated to Raise Money for Cystic Fibrosis. I cant wait to see how much we can raise together. I will be getting the chop to my shoulders in only a week and a half (or so)! I'm so excited to help make a difference in the lives of people who suffer from CF. If you want to donate, I have the link in my bio - from 50 cents to $5 - you can help make a difference ❤ #cysticfibrosis#fundraiser#raisemoneyforcharity#donate#donatinghair#helpmakeadifference