Liste des hashtags les plus populaires par sujet #VASCULITIS

Las lesiones vasculares son variadas y representan una causa importante de dolor y consulta. Muchas veces se confunde el dolor de traumatología con un dolor de origen vascular. Lo importante es: ante la duda siempre consultar con un especialista. . . Trombosis: Formacion de un coagulo de sangre en la luz de un vaso sanguíneo . Compresión: Es la presion externa ejercida sobre un vaso sanguineo por otro cuerpo . Embolia: Obstrucción de un vaso sanguíneo . Vasculitis: Es la inflamación de los vasos sanguíneos . Espasmo: Es la contracción del musculo liso ocasionando una disminución del flujo sanguíneo . Secuestro/Desviación: Es la disminución del flujo sanguineo en una rama por disminución del diametro de su luz ocasionando acumulo de presion antes del obstaculo generando desviación a otras ramas cercanas . Ateroma: Es la acumulación de una placa de grasa en la capa interna de una arteria . Hiperviscosidad: Es la resistencia en el fluir de la sangre debido a la adhesion y cohesion de sus componentes (proteinas plasmaticas, globulos rojos, plaquetas... ) #cirugía #cirugiacardiovascular #cardiovascular #ccv #embolismo #vasculitis #vena #vaso #arteria #vasosanguineo #trombosis #tep #tvp #tromboembolismo #tromboembolismopulmonar #embolia #trombo #plaquetas #sangre #hb #hemoglobina #vasculitis #espasmo #vascular #ateroma #lesionvascular #inflamacion #anticoagulante #coagulacion #dolor #edema

i have takayasu’s vasculitis, a rare disease with no known origin or cure. i have lived 9 years with it, beyond what any medical professionals could’ve imagined. everyday i am cognizant of the miracle & testament that truly is my life. i am honored to be in this vessel and to share my story with others. i know i am not alone in my fight. tap the @viceidentity link in my bio to watch & hear a piece of my journey. bless - - - - - - #chronicillness #spooniesofcolor #raredisease #vasculitis #spoonielife #spooniesupport #healthadvocate #chronicallyill #invisibleillness #healthjourney #spooniecommunity #fibromyalgia #bloodclot #arteritis #nycmodel #nyc #wellnessjourney #wellnesswarrior

Have we met yet? If we haven't, I'd love to introduce myself and also meet you! We have a lot of new followers here at LupusChick and I am Marisa, its founder (and also LFA board member). I was diagnosed with Lupus 17 years ago at the age of 23 and started LupusChick a few years after that at the same time my journalism career began. What started out as a blog grew into a community and nonprofit that reaches almost 500K people per month! We are comprised of men and women of all ages who deal with lupus and overlap disease, and other chronic illnesses. Our mission is to build a strong community of people who can go out into the world and share their story and raise awareness. On the nonprofit side, we focus on education and have given away 7 partial scholarships to people in college who live with lupus. Over the years, I have personally dealt with multiple strokes, two brain aneurysms, heart involvement, vasculitis, a blood clot, a year in a wheelchair, and some other crazy issues. I am blessed to have an amazing support system of family and friends who have helped me get through these rough seasons. My faith is also solid and I know that God has helped me get through all of the things that come along with a lupus diagnosis. I am current writing an inspirational memoir of this chronic illness journey and can't wait to share it with you all. Lives are changed through the sharing of stories, so shout yours from the rooftops♡ If we haven't met or chatted yet, you can drop me a line anytime! Either here, on our FB page, or directly to my inbox through our site www.lupuschick.com (go to the contact page). I'm so glad you are here and are a part of our community ✨ #lupus #lupuschick #nonprofit #leader #spoonie #lupusawareness #lupussupport #lupuswarrior #support #encouragement #faith #hope #autoimmune #fatigue #vasculitis #brainaneurysm #stroke #strokesurvivor #lupusadvocate #lupusawarenessmonth #wolfpack #lupuswolfpack #memoir #writer #journalist inspiration #hybridmemoir #God #memoirist #christian

Most people don't realize that chronic illness flares can happen at any moment, and the anxiety that often comes with those unknowns. While someone may or may not be "visibly sick," that doesn't always mean the anxiety and fear disappears. ••• My name is Julia (@julia.metraux) -- The Mighty's chronic illness editorial intern (that's me in the photo above!). Today, follow my journey on our instastory, where I'll be talking about the ins and outs of pursuing treatment for chronic illness and rare disease. If you've struggled with the fear, stress and anxiety (and don't forget about the physical symptoms) of illness, follow me today! ••• What are some of your fears and worries as someone who lives with chronic illness or rare disease? Tell me in the comments below. ••• #invisibleillness #vasculitis #chronicillnesswarrior #chronicfatigue #cysticfibrosis #chronicillness #spoonie #spoonielife #fibromyalgia #fibro #chronicpain #chronicallyfabulous #lupus #crohns #crohnsdisease #ulcertaivecolitis #spooniecommunity #disability #mentalhealth #anxiety #mentalhealthwarrior #ehlersdanlossyndrome #potssyndrome #endometriosis #endowarrior #themightysite #myrarelife

When I was 24, I met my husband. A few short months after that, my leg went numb. Little did we know that this was my first MS symptom. It would take 15 years to figure out what was going on and find out I have Multiple Sclerosis. Back then MS wasn’t easy to diagnose. _ My autoimmune disease attacks the central nervous system and often leads to a life of paralysis and disability, spent in a wheel chair. You’ve all seen the toll it’s taken at times on MS warriors like @terrywahls and @selmablair ❤️ _ Last fall, my symptoms flared to the worst they’d ever been. After I was discharged from the hospital, we saw many of the best neurologists in the world. That’s when we were told I’d been living with this disease for over 26 years. _ At times I compartmentalize my disease, and sometimes it helps. Not thinking about my illnesses (I also have 2 other autoimmune diseases -- Celiac Disease + Hashimotos Disease, as well as the BRCA mutation) helps me keep my chin up each day. Until it doesn’t, and the fatigue and symptoms slap me in the face. This is what living with autoimmune disease looks like for so many of us. 1 in 5 people suffer from AI disease and 75% of us are women. _ I’m talking about this to remind us all that we’re not alone, we have each other. And more than anything, it’s OK to talk about it. _ I remind myself every day to be kind to my body and mind, heart and soul. And I think about how lucky I’ve been to have this community of health foodies like me, ever since I went grain-free in 2001. I’m so grateful to be on this healing path with you. _ Thank you from the bottom of my ❤️. I am very truly blessed and I love you guys. _ To find out more about MS, click the link in my profile and go to What is MS: https://elanaspantry.com/what-is-multiple-sclerosis/ _ _ #autoimmunedisease #autoimmune #autoimmunedisorder #MS #multiplesclerosis #celiac #celiacdisease #hashimotosdisease #hashimotos #hashimotosthyroiditis #hashi #graves #ulcerativecolitis #UC #IBD #diabetes #lupus #rheumatoidarthritis #lymedisease #scleroderma #psoriasis #vitiligo #vasculitis #hepatitis #alopecia

GUYS!!! a day I will never forget has arrived!! My mother who is in renal failure has been MATCHED with a donor in Wisconsin!!!!!! I am gushing with happiness as this process has been a tough one. She has a very high rate of reactivity and her transplant team worked hard to find her the perfect one, one that she hopefully won’t reject! I am overwhelmed with the amount of friends and family who tried to donate during this process. You have no clue how humbling it has been. The surgery is set for May 29th and my brother will be donating to someone else for her— a transplant chain. Please keep my sweet mama and brother in your thoughts as well as her amazing team that is working hard to keep her healthy. ♥️♥️

12 yıllık Romatoid Artrit hastamız... Bize kaplumbağa terbiyecisi tablosunun 1.500 parçalı puzzle ını elleriyle yapmış. Elleriniz dert görmesin diye kendisine en içten dileklerimizi iletiyoruz... #artrit #arthritis #rheumatoid #romatoidartrit #romatizma #ağrı #saglik #sağlıklıbeslenme #sağlıklıyaşam #ankilozanspondilit #belağrısı #lupus #rheumatoidarthritis #gaziantep #raynaud #vasculitis #vaskülit #gut #gout #skleroderma #scleroderma #ağızyarası #aft #omurga #omurgasağlığı

Illustration by @mellow.doodles Go follow . "Most importantly, don’t wait until you reach crisis point to look after your mental health. You wouldn’t do it with your physical health. Your mental wellness effects literally EVERY area of your life. I’ve seen it happen with so many people, and experienced it personally - neglecting to proactively address looking after ourselves is so damaging and ultimately leads to disaster, chaos or crisis. Make it a priority in your life, step by step. It will always be worth it " . #mentalhealth

#rarediseaseday is something i celebrate everyday. in 2011 i was diagnosed with takayasu’s arteritis, a vascular disease which affects only 2 in every million people. i was told by numerous medical professionals in different cities and hospitals that i wouldn’t live to see 21, but here i am at 29, flourishing in my triumph. everything about my life is a miracle —it’s simply divine. my higher power, my god, my light, my ancestors, my faith and courage had me covered during some of the craziest and hardest days of my life, some which i still face from time to time given the unpredictable nature of the disease. testing my inner and outer strength will be an ongoing process, but the power that surrounds me is thick and impenetrable. being enlightened is a gift i had to work hard to achieve. i am proud, i am grateful. tag someone who needs to know this message. - - - - - #rarediseaseday #survivor #enlightenedbeing #higherconsciousness #wellnessjourney #wellnesswarrior #healthadvocate #spoonie #spooniewarrior #invisibleillnessawareness #invisibleillnesswarrior #takayasusarteritis #vasculitis