#ibdday

[zena-dawn]

On this ‘World IBD day’ I want more people to understand what we go through each and every day. I want to make people more aware of and understand that there shouldn’t be a stigma around the subject and that talking about ‘poo’ isn’t ‘taboo’!! Oh and while we are on the subject having and talking about ‘stoma’s isn’t taboo’ either. IBD is a autoimmune disease and unfortunately people (myself included) usually suffer with multiple autoimmune diseases/illnesses at the same time. Many of which like IBD are incurable and lifelong. #ibdday #ibdawareness #crohnsdisease #invisibleillness #chronicfatigue #nocure #makinginvisibleillnessesvisible #lifelong #stoma #stomaawareness #ileostomylife (at South Wales) https://www.instagram.com/p/Cdu4SLEON4L/?igshid=NGJjMDIxMWI=

[thats-just-life-i-guess]

World IBD Day today. Inflammatory Bowel Diseases are chronic conditions that you’re stuck with for the rest of your life. There’s no cure. Medications can help put you in remission, or they might not. It can take a while to be diagnosed, then just as long to get the right medication. If medication doesn’t work, you could end up having surgery. I’ve had two surgeries and now live with a stoma.

IBD is an invisible illness and causes a whole range of symptoms, including diarrhoea, fatigue, weight loss and stomach pain and cramps.

IBD can have a large impact on people’s lives. It can affect work lives, home lives, social lives, mental health, physical health, pretty much any aspect of someone’s life. The severity varies from person to person, but the one thing we all have in common is that we want to raise more awareness for people with IBD.

[crohnieblog-blog]

It's #worldibdday..

Hope you have all woken up feeling good! Today is the day to raise awareness, share stories, support each other and be united.

Do what you can to help other understand this diseases, but most importantly be there for each other. We have good times and we have bad times, we are in this together.

Stay strong, YOU are doing so well.

World IBD Day 2018.

[virag-0]

A small sneek peak into my life for #IBDday I was in the emergency room for 5 hours due to severe stomach pain and vomiting. My symptoms are real. My ulcerative colitis is real. My diseases are real. I fake nothing. When i hear stories of people faking illnesses, it pisses me off to the nth degree. No one, and i mean no one, deserves to live in this kind of pain. I have seen my mother cry, hover over me, and hold my hand as i cry. I am her baby; her bear cub. She has protected me every second of every day. Even when we fight. #IBD #UlcerativeColitis #iamautoimmune

[wanderlustingriver]

Tonight major Canadian landmarks turned purple for #IBDDAY Hopefully these lovely purple structures caused some attention and had people wondering what it is for. I hope some how that people discovered that the lovely purple represents Crohns and Colitis. 💜💜 #PurpleRibbon #GetYourBellyOut

[ash-hole-ish]

Today is world IBD day! What a day to be alive, literally. I've suffered from Ulcerative Colitis for 6 years now, and although I have a handle on things mostly, it's still a very scary thing to suffer from. I almost never look sick, but inside my insides are usually ripping me apart. Today is for us, for us that have made it a part of our lives, but not our whole lives. Today is to celebrate our lives, and to bring a little awareness to those who don't know. I sport purple for all those suffering from any autoimmune disease, and mostly for myself, because I couldn't be more proud that I haven't given up when I've wanted to so many times. I'm here, and life is beautiful! 💜💜💜💜💜💜💜💜💜💜 #worldibdday #ibdday #wearpurple #ulcerativecolitis #celebratelife

[suznvilaga]

Május 19 - Egy újabb világnap. Az én, a mi világnapunk. Az IBD betegek napja. Kérlek Téged, aki talán még sosem hallottál erről a kórról, segíts egy megosztással, hogy minél több ember tudomást szerezzen róla. Lehet, hogy kívülről nem látszik, de igen, sajnos sokan szenvedünk ebben a - tudomány jelen állása alapján - gyógyíthatatlan betegségben. Lehet, hogy nem mondjuk, de sokszor fáj. Oszd meg és segíts! Nem kell más, csak egy kis figyelem. Olvass utána, kérdezz meg bennünket. Részemről a blog ennek a terápiának a része. Gyógyítom vele magamat és próbálok a Többieknek segíteni. http://suznvilaga.hu/category/crohnnal_az_elet/ "Ezekkel takargatom a sebeimet és a fájdalmaimat. Lelkieket és a Crohnból eredőeket. És ezt tudom, hogy sokan nem tudják. Nem tudják, mi van a ’színpad mögött’. Nem fogom mindenkinek elmondani, hogy megértse, mert van, aki ha elmondom, sem fogja fel. Ez nem az én hibám. Ha ők azt hiszik, hogy nekem a legnagyobb bajom életemben az volt, hogy a barátnőm nem szólt a kávézóban, hogy elkenődött a szemfestékem; higgyék. Nekem néha fájdalomcsillapítóként szolgál a felületesség, és segít túlélnem. És míg vannak, akik elolvasnak, addig írni fogok. Írok jóról, rosszról. Apró örömökről és kapitális tévedésekről. Mert jólesik. Nekem is, és úgy látszik, Nektek is."