#chroniccondition

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sadie.yoga. I'm late again, it's a chronic condition I inherited from my father's

I'm late again, it's a chronic condition I inherited from my father's side 😂 #truestory😐 Sunday was day 5 of #HolidayAsanas and brought us #PuppyPose or #UttanaShishosana I'm taking a creative variation today... To show off my cute socks! 😅😅😅 ______________ Hosts: @whitneydavisyoga @warriorfromwithin @yogi.jodie @kelleyapril @freckled_yogi @bentley.likethecar - - Generous Sponsors @aloyoga 🥰 @alomoves 🥰 - - Pose line up: Malasana ✔️ Padmasana ✔️ Extended hand to big toe pose ✔️ Anjaneyasana ✔️ Puppy ✔️ Wild thing  Bow Fish Hero  Pigeon #alwaysrunninglate #chroniccondition #atleastimhonest #honestyogi #yogiinsocks #christmassocks #sockyoga #bodyposiyogi #thighsout

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a_chronic_princess. Now I am fairly sure that this is not your water bowl Bella! Good job

Now I am fairly sure that this is not your water bowl Bella! Good job Sidney is so laid back he didn’t even bat an eyelid. If however she had gone for his food ... well I don’t think we would have a cat left!! #assistancedogsuk #assistancedogs #assitancesdogintraining #furbabies #cat# #spinalinjury #invisiblecondition #chroniccondition #spondiolesthesis #backpain #eds #invisibleillness #jointpain

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disabledtravelwithgeorgina. ‘Life is uncertain. Eat dessert first.’ -Ernestine Ulmer 🍰🍪🍩🍨 I ha

‘Life is uncertain. Eat dessert first.’ -Ernestine Ulmer 🍰🍪🍩🍨 I had a wonderful pancake brunch at Bistro Guy when Richard and I visited York! Pancakes have literally been around since the Stone Age, although I’m sure the recipe has had a few tweaks since then! They’re such a massive treat for me and I will jump at any excuse to have dessert instead of lunch haha!😂😂 If you want to read about the access at Bistro Guy then check out my blog post on https://disabledtravelwithgeorgina.blogspot.com/2018/12/bistro-guy-york-restaurant.html!💖 #ChronicCondition #chronicpainsucks #chronicbackpain #chronicpainawareness #chronicwarrior #chronicillnessawareness #chronicallymotivated #chronic #chronicpain #ChronicFatigue #chronicallyill #chronicpainwarrior #chronicdisease #chronicillnesswarrior #ChronicFatigueSyndrome #ChronicLife #ChronicallyFabulous #chronicillnessawareness #overcomingadversity #wheelchairwarrior #wheelchairprincess #lifeonwheels #sciawareness #wheelchairwoman #onwheels #wheelchairgirl #wheelchairbarbie #disabledandcute #babewithamobilityaid #spoonie

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a_chronic_princess. So someone woke up from her nap screaming because of #teething and Sid

So someone woke up from her nap screaming because of #teething and Sidney came to comfort her. He has the magic touch as she stopped screaming for a while!! #assistancedog #furbabies #bestriends #furfriend #spinalinjury #invisiblecondition #chroniccondition #spondiolesthesis #assistancedogsuk #esd #chronicpain #backpain #jointpain #disabled #disablemum #ivfjourney

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sarahmorethanacurvedspine. I ordered my online food shopping order yesterday. It was delivered at

I ordered my online food shopping order yesterday. It was delivered at 3:50pm (UK) today. I got these Christmas things in my order. I bought the Rose' wine gift set, for a Christmas present for myself. If you have a #disability or condition like me, do you sometimes order food shopping online? Can you go shopping on your own? I can't go shopping on my own because I use a wheelchair a lot when I go out (a wheelchair that someone pushes me in) because I get tired walking because of my #scoliosis and I need someone to push me in my wheelchair. I can walk a bit. What disability or condition do you have? This question is for everyone who does an online Christmas food shop, what Christmas things do you buy to eat and drink over Christmas? #bloggers #bloggeroninstagram #christmas #christmasshopping #christmasfood #christmasfoodshopping #onlineshopping #onlinefoodshopping #festivefood #festivedrinks #disabledbloggers #disabilitybloggers #disabled #physicaldisability #chroniccondition #scoliosiswarriors #christmastreats🎄 #christmastreats #freixenetrosé #rosewine #heroeschocolate #mincepies #asda #bloggersworldwide #ukblogger #lifestyleblogger

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ciaras_journey_. 🤷‍♀️🙈 Yes please!!
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Between migraines & feeling like my body is tr

🤷‍♀️🙈 Yes please!! . Between migraines & feeling like my body is trying to go against me again, I've been feeling quite ill over the last week. I was up in Dublin for the week but spent a good bit of it dealing with an awful migraine & all of it's lovely side effects. Once I got over that (sort of any way) my joints started playing up, awful cramps & really painful when walking. I just blamed the weather as it's been strom after strom here recently but now I'm seeing more little spots appear on my arms & legs so I'm hoping it's not going to end up as a full on flare 🙈 I'm not ready to deal with all of what that intales just yet. In saying that, the bad patches on my legs, have had some skin come through & clear up a bit of the Psoriasis in places. With that I'm pleased as it also shows me that using the coconut oil has been helping 🤞. So from tomorrow on I'm going to up my use of it & also use it on my arms to try calm them down again as this is the 2nd time these little spots have showed up lately. Also, I think it's crazy that it's Christmas Eve this time next week!!! 🙈 ______________________________ Be kind to yourself 💖 ______________________________ . #psoriasis #livingwithpsoriasis #longtermcondition #chroniccondition #psoriaticarthritis #arthritisawareness #arthritiswarrior #psoriasiswarrior #psoriasiscommunity #psoriasissupport #migraine #fatigue #curearthritis #pcos

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spoonie_village. #fordayswhenyoudonthavetheenergytosayit  Due to symptoms it can be har

#fordayswhenyoudonthavetheenergytosayit Due to symptoms it can be hard to keep on top of letting everyone know there’s no change or you’ve had a bad time of it lately. I’m having quite an okay time lately after the hell of the last few months but, this came about as a kind of sarky reply to a comment I’ve heard often when I had to take a break from things the whole “ooh I thought you’d disappeared ha ha” thing. Truth is nope, we don’t disappear we go into the difficult place where managing illness and life is the only focus so you can make it through the day. No disappearing acts or choosing not to turn up or take part, it’s called survival mode and without it we’d never again have the energy to show up at any time. Never feel ashamed or wrong for taking time out to recover, rest and get yourself back to a point of your normal, because I always find too those people who make such passing comments are never the ones to check up on your wellbeing or show concern anyway, rather they’d just make a dig about it because it’s just a complete lack of understanding what you go through and they often have very little interest in actually finding out. It’s okay to put your needs first. 💖

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savvy_coop. Have you been diagnosed with #asthma? Do you use #Nucala to help contr

Have you been diagnosed with #asthma? Do you use #Nucala to help control your symptoms? You may qualify to earn $150 for a 60-minute interview in downtown Philadelphia--tomorrow--Tuesday, December 18 or Wednesday, December 19. Link in bio under Gigs to apply.⠀ .⠀ .⠀ .⠀ .⠀ #savvygig #askpatients #medication #chroniccondition #chroniccough #coughing #lungs #steroid #healthcare #patientexperience #patientengagement #patientcentricity #savvycoop

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_ginandginger. 🔥There’s always room for more learning.

🔥There’s always room for more learning.

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psoriasisuk. 50 for 50 Project - Mia’s Story
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I'm Mia and I am 21 years old. Growi

50 for 50 Project - Mia’s Story . I'm Mia and I am 21 years old. Growing up I had no problems with psoriasis, with the skin condition only showing itself shortly after my 18th birthday. . I had just left home for the first time and moved to Leeds to start university, everything about the experience was daunting but shortly after moving I settled in. After a month of living away, I started to notice a rash on my arms. I presumed this was just caused by the stress of moving and decided to ignore it, hoping it would disappear. A week down the line, the rash was still on my arms and spreading on my legs. Before I knew it, all my arms and legs were covered in sore, red, flaky plaques. . I had numerous trips to doctors and received numerous different creams/steroids to try and help but none of them did. The condition has made a huge impact on my mental health. I was living in a city with new people, now with what I saw as awful skin. I presumed people would want to stay away from me because of this condition. I have suffered from both depression and anxiety since my skin began to flare. I know my psoriasis was a huge factor in the development of these mental health problems. . After living with the condition for three and a half years I am starting to accept it will always be there. I have recently undergone 8 weeks of UVB treatment which helped for as little as a month before my psoriasis came back. . I accept my skin as part of myself now. There will always be days I struggle with the condition and my outlook of it but I can now deal with that. I have luckily had the most supportive friends and family around me while I have been dealing with the mental side of the condition, who are there to pick me up on the days it gets me down. . #50thanniversary #psoriasis #yourstory #PsoriasisAssociation #psoriasisuk #psoriasisstory #skin #stress #plaquepsoriasis #psoriasistreatment #psoriasistreatments #mentalhealth #depression #anxiety #psoriasissupport #chroniccondition #longtermcondition #psoriasisawareness #psoriasisjourney #psoriasiscommunity #livingwithpsoriasis #psoriasishelp #psoriasislife #psoriasisproblems

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jo_josmo81. An article on BBC news today - talking about the link between ME and a

An article on BBC news today - talking about the link between ME and an Over active immune system. ✨ This makes some sense I think and im really glad new research is being done and that ME is being talked about in mainstream news - I just wish they would be careful about their wording “Chronic fatigue syndrome is a long-term illness characterised by extreme tiredness. “ ( taken from the above article) ✨ They do go on to use the word ‘fatigue’ but ‘extreme tiredness’ is very misleading to those who do not know about this condition - - - - - #myalgicencephalomyelitisawareness #myalgicencephalomyelitis #millionsmissing #invisibleillness #invisibleillnessawareness #chroniccondition #chronicconditioncollector #chronicspontaneousurticaria #chronicurticaria #awarenessisneeded #fatiguenottiredness #bbc #bbcnews

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gcphn. If you're managing a #chroniccondition, #MyHealthRecord can help you t

If you're managing a #chroniccondition, #MyHealthRecord can help you to coordinate treatment with multiple healthcare providers, so that everyone is on the same page when it comes to your care. Find out more: http://bit.ly/MHRChronicConditions

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chronicthriver3700. I can’t believe I have actually gone down a dress size in two weeks. I

I can’t believe I have actually gone down a dress size in two weeks. I don’t own a set of scales as I have two teenage daughters who don’t need that kind of pressure in their life. But wow I’ve not even tried! I’m not that mobile so I don’t/can’t exercise but this has made me feel fantastic! Along with mental clarity and boosted energy levels I’m going into the new year feeling positive xxx #blog #blogger #blogging #blogginglife #lifeblog #bloglife #thriveexperience #thrive #thrivelevel #levelthrive #levelthriveexperience #thrivelife #thrivelifestyle #3simplesteps #itreallyworks #weightloss #limitedmobility #chronicillness #chronicpain #chronicfatigue #chroniccondition #spineinjury

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provhealthsc. Looking for a gift for a friend with a #ChronicCondition? Laurens Hope

Looking for a gift for a friend with a #ChronicCondition? Laurens Hope creates attractive jewelry that can literally save a life with a #MedicalID. Bohemian, sophisticated, ornate or simple, they have it. And they're offering holiday sales! www.LaurensHope.com

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And that’s a wrap! A huge thanks to our new Team of Advisors for spending the last two days with us at PatientsLikeMe. We can’t wait for all next year has in store! 💛

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chronicthriver3700. There will be a new blog post up on my website over the weekend about

There will be a new blog post up on my website over the weekend about coping with Christmas for chronic condition sufferers. I can’t stress enough how much Le-vel Thrive Lifestyle 3 simple steps has helped me when I needed it. Xxx #blog #blogger #bloggerlifestyle #lifeblog #bloglife #limitedmobility #chronicillness #chronicfatigue #chronicpain #chroniccondition #levelthrive #thriveexperience #3simplesteps #thrivepromoter #levelthriveexperience #thriveexperience #itreallyworks #healthyliving #healthylife #health

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endoproelium. This week has been unbelievably hectic. I'm now sat down with some pat

This week has been unbelievably hectic. I'm now sat down with some pate on toast and a cup of tea watching a movie on Netflix. Got my laundry in the machine and other than that it's now time to relax before my birthday tomorrow. #Done . . . #Endoproelium #Endometriosis #Endo #EndometriosisWarrior #EndoWarrior #EndometriosisAwareness #EndometriosisAware #EndoAware #EndoSister #EndoMonster #EndoStrong #ChronicCondition #ChronicIllness #InvisibleIllness #PainLevelSquiggles #YouDontLookSick #Pain #Tired #Fatigue #FrozenPelvis #Surgery #ExcisionSurgery #Excision #Recovery #Exhausted #Hectic

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My little snuggle buddy and I pretty much in our favourite spot. The bed!😂🐶 I love this handsome little furry guy so much. He always makes me smile. 😊❤ I really wish I could sleep for more than a few hours straight and don't feel so tired after every night and nap I take. Chronic fatigue really is a struggle. And I definitely wish that my CRPS wouldn't act up so bad as soon as I try to rest. I mean, I understand it's flaring, when I'm doing much or from weather changes or when I'm getting emotional, but I don't understand why the hell my symptoms worsen when I lay down and do nothing at all. Come on CRPS give me a break...☹ It's gotten to that point that almost my whole arm gets extremely hot and red and my pain goes through the roof every night. It really worries me, because I feel like it gets worse... Skin changes were just localized at my hand and wrist in the past. Now, they go up almost my whole forearm...The pain also went up higher. I just hope that this is just because my nerve block wears off and/or the cold weather...I guess, I will find out eventually. 🙈 Tomorrow I head to my pain clinic for my next nerve block. I'm very grateful that I'm getting these blocks every few month now. 🙌😊 Hope you all are okay!🧡🧡🧡 #crpsawareness #crpswarrior #crpsreallygetsonmynerves #crpsrsd #crpssucks #crpsflare #crpslife #chroniclife #chronicillness #chronicovercomer #chronicpain #chronicfatique #fatigue #chroniccondition #chronicillnesswarrior #snugglebuddy #parsonjackrussell #jackrussell #jackrussellofinstagram #ilovedogs #ichoosejoy #dowhatyouthinkyoucantdo #dontforgettolaugheveryday #grateful #nerveblock

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Behind the scenes with the 2019 Team of Advisors! We can’t wait to introduce you to these rockstars.😎

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thevftos. I’m feeling very Christmassy today!! (Not long til the big day folks!)

I’m feeling very Christmassy today!! (Not long til the big day folks!) I’ve even uploaded a video to my channel about how YOU can donate for FREE to the @cftrustuk or any charity of your choice, just by shopping! 😱 • So whether it’s ASOS, Amazon, New Look, John Lewis, Tesco (the list literally goes on) you can donate a percentage at no extra cost! How flippin cool is that! So if you still have some Christmas shopping left, or even if you just want to get something for yourself then check out the video, link is in my Bio!🕺 • P.S I don’t actually edit videos with fairy lights draped over my laptop and baubles surrounding it... but it looks so FESTIVE! 😬🎄🤷🏼‍♀️

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psoriasisuk. She did it! Eleanor finished the Malaga Half Marathon in 2:30:09, well

She did it! Eleanor finished the Malaga Half Marathon in 2:30:09, well under her target time of 2 hours 45 mins! Well done Eleanor! . She’s also managed to raise over £300 (inc. Gift Aid) for the Psoriasis Association - What a star! 🌟 . You can still support Eleanor by donating via her fundraising page at uk.virginmoneygiving.com/EleanorHawkins1 . #Malaga #running #psoriasis #livingwithpsoriasis #MalagaHalfMarathon #PsoriasisAssociation #psoriasisuk #psoriasissupport #psoriasisawareness #fundraiser #fundraise #fundraising #fundraisingevent #charityevent #charity #donate #longtermcondition #chroniccondition #skin #psoriasiscommunity #psoriasishelp #psoriasislife

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luann.riley. As a person that navigates a chronic condition, there is a form I comp

As a person that navigates a chronic condition, there is a form I complete each month when I see the specialist. The purpose of the questions is to gauge the impact of the condition or illness on quality of life because that is often how insurance companies approve or deny treatment. ⠀⠀ The first time I saw Dr. Blake, she noticed that the question, “how many days did your condition require you to miss optional social, leisure, or family functions?” had a zero beside it. She said, “how can I that be?” And I told her with tears in my eyes that at some point I just stopped saying “yes” to parties, girls nights, dinners, or anything “extra” socially because I knew without a doubt I would have to endure it with a headache. Rather than disappoint my friends and family or suffer through with a killer headache, it was just better to say no. The required events of my life were all I could sign up for and even those didn’t have a zero beside them. ⠀⠀ When @chrisykeller invited me to this gathering Monday night, for a split second that old feeling of “what if” creeped in and I almost said “no” just in case. But I didn’t. I texted what felt like a brave YES. ⠀⠀ As I was leaving my house, the reality hit me that I was going to a holiday party without a headache. I wept. I am slowing regaining control of my LIFE and it’s a GIFT. ⠀⠀ Friends, if this is a season where you have to say no to all the extras because that’s what’s best for you, do it and be gentle to yourself. ⠀⠀ If you have people in your life that you know it’s hard for them to commit socially for whatever reason this season, give them grace and hug when they say “no” but never stop inviting them. Their miracle could be right around the corner. ❤️ ⠀⠀ #braveandboldfaith #chronicillness #chroniccondition #occiptialneuralgia #5monthspostsurgery

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jodiewigg. George is keeping me company 🐈
After a busy weekend & yesterdays Xmas

George is keeping me company 🐈 After a busy weekend & yesterdays Xmas shopping trip, I now need to allow myself to rest. My back is hurting a lot more than usual so moving is painful. Does anyone know of anything that may help? . . . #cat #catsofinstagram #pain #backpain #fibromyalgia #fibro #fibroawareness #fckfibro #fibrowarrior #fibrofighter #chronicillness #chronicpain #chroniccondition #invisibleillness #butyoudontlooksick #spoonie #spoonielife #depression #anxiety #fatigue #mentalhealth #rest #selfcare

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delmonrehab. اسمح لفريق رعايتنا المنزلية بالتخفيف من الضغوطات ومساعدة من تحبهم على

اسمح لفريق رعايتنا المنزلية بالتخفيف من الضغوطات ومساعدة من تحبهم على الوصول للحالة الصحية الجيدة. اتصل بنا اليوم. Allow our in-home care team to alleviate the stress of helping a loved one navigate life with a chronic health condition💛. Contact us today 📞. #DelmonRehab #ChronicCondition #HomeCare #رعاية #دلمون

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dralamiskids. Even if your child seems really sick, don't give more medicine than th

Even if your child seems really sick, don't give more medicine than the label says. It won't help your child feel better faster, and it may cause harm. Call us today to consult with our pediatrician. :) . . . . #pediatrician #pediatrics #childdoctor #immunization #childcare #childhealth #physicals #physical #preventivecare #childinjury #flushot #sickvisit #screenings #sportsphysicals #chroniccondition #behavioralhealth #childbehavior #teenmedicine #adolescentmedicine #adolescenthealth #doctor

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a_chronic_princess. So Saturday Sidney went on his First Ladies what lunch and he did very

So Saturday Sidney went on his First Ladies what lunch and he did very well! It was lovely having him with me although I think he got a bit fed of us talking by the end of it!! #spinalinjury #invisiblecondition #chroniccondition #spondiolesthesis #assistancedogsuk #eds #invisiblecondition #chronicfatigue #pain #jointpain #backpain

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_ginandginger. 🔥Chase your interests.

🔥Chase your interests.

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_ginandginger. 🔥Shine and shimmer.

🔥Shine and shimmer.

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