#cfs

249,705 posts tagged with #cfs

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I am LOVING watching my healing journey... in just a bit over 2 months I have gone from sooo sick I could barely drag through the day, not wanting to move one extra bit I didn’t have to... to now starting to have enough extra energy for things like going Fishing which has always been one of my most favorite pastimes! . I know I have a long way to go, and my road to health will ever be a challenging one, but I am here, I am living, I am fighting for it and reaping the rewards of my work and dedication. . Thank you PLANTS for my healing!

Another repost from @catanacomics because it couldn't be more Dan and I if it tried 😂 . Hope you all had a lovely Easter Bank Holiday in the sunshine 🐣 I spent it doing a lot of resting and a bit of sorting out as and when I could manage because my fatigue and pain levels have been pretty shite but I think that the quick changes in weather haven't helped, does anyone else find that? 🤷🏼‍♀️ I've been trying my very best for the past two weeks to push myself to go out with Poppy every day (so long as it's not raining, because she's a Princess and hates it!) so that I get out of the same four old walls and get some fresh air, but mostly to not let my anxiety beat me so much 😕 It's been going really well and if I'm honest, I'm kind of proud of myself for that- we've even been going the 'long way round' on the way home sometimes 💪🏻 . . (✏ - @catanacomics) . . #trying#surviving#doingmybest#spoonie#chronicallyill#chronicillness#invisibleillness#behcets#behcetsdisease#fibro#fibromyalgia#chronicfatiguesyndrome#me#cfs#myalgicencephalomyelitis#chronicpain#depression#anxiety#invisibleillness#spoonielife#daytoday#instadaily#instajournal#instadiary

Went out with our pussy 🤣 So proud of her trying to explore the outside world with ofc our door wide open and us in arms reach 😆 Also love my new hoodie❤😎 #rescuecat #chronicillness #cfs #selfdiagnosis #spoonie #spoonielife #love #bisexuell #bipride #trans #transboy #agender #ftm #dysphoria #battlingmentalillness #agenderpride #transpride #lgbtqpride #lgbt #battlingmentalillness #babyboy #edgy #grunge #friendsfan #relationship #depressedbutwelldressed #gamerboy #gamer #rescuecat #chronicillness ----------------------------------------------------------------- Repost:@the_black_sheep_666

At the going down of the sun, and in the morning.. we will remember them. #anzacday #anzac #australia #cfs #countryfireservice #sacountryfireservice #youthvigil #blackwoodwarmemorial

Hello and welcome to my account :) I have decided to make an account dedicated to my struggles as a teenager who sufferers with mental and physical illnesses . ~ I am a girl who is 17 , bisexual , living in england. I am currently on a gap year and love baking and drawing and cats ~ I suffer from bipolar type 2 , anxiety and self harm ,am part of CAMHS in the uk My physical illness are HCM , CFT, hypermobility, and undiagnosed GI issues. ~ this is account is for me to hopefully find some friends going through similar issues and to help myself by getting things out my system haha. Feel free to DM 🖤 • • • #ventaccount #chronicillness #mentalhealth #mentalhealthawareness #bipolar #cfs #hcm #eds #chronichealth #newaccount #tryingtolive #selfharm #anxiety #awearness #mentalhealthmeme #meme

Kids have endocannabinoid systems, too! ✨ . . Cannabis medicine is not specific to age, race, gender or any other title. From sea squirts to humans, we’ve all got em! 💚 . . Balancing our endocannabinoid systems is IMPORTANT! By introducing hemp into our daily diets , we regulate or entire body and prevent so many unnecessary diseases. 🌱 . . @cultivatehope_chemovar stands by the unpopular opinion that cannabis is great for children. We have seen first hand what life is like with, and without, cannabis medicine for children who need it. 🧠 . . Learn more about cannabis medicine at www.cultivatehopechemovar.com and shop our selection of HOPE 💚 . . Together, we will find HOPE For a Better Tomorrow ☀️

This year, 15 projects suggested by the Georgia Southern community were funded by Student Sustainability fees. They were highlighted on Monday at the Sustainability Showcase. #cfs @gasouthernsustainability

No idea what I was laughing at, but I was pretty tired by this point, so I was probably delirious. 📷 - my mum #inthewoods #nobodycanhearyouscream #disability #cfs #disabledhikers #teamsticks

Modelo utilizado pelo Everton na temporada 2003/2004. Na ocasião o clube celebrava 125 anos de história e seu elenco contava com o jogador que entraria para a história como o maior artilheiro da história da seleção inglesa. Essa e outras diversas camisas do Everton você encontra no nosso site. #futclassics #camisasclassicas #classicfootballshirts #cfs #evertonfc #everton #premierleague #pumafootball #camisasantigas #camisasdefutebol

Our 2nd Care Fair celebration is in 4 days! 😍 Come to indulge in: -physical therapy & chiropractic (realign!)👈 -massage & acupuncture (release!) 💆 -yoga & stretching (relax!) ✌️🙏 -fresh🍎, healthy 🥦 and delicious 🍪eats (yum!) -engage in community through art and activities (express yourself!) 🎨 -photo booth shenanigans 📸 -surprise gifts to take home! 🎉 To RSVP: https://wellacopia.us/carefair Date: Sunday, April 28th Time: 3-6pm #invisibleillness #spoonie #fibromyalgia #chronicillness #autoimmunedisease #ibd #raynauds #disability #hashimotosdisease #ulcerativecolitis #adrenalfatigue #chronicpain #lyme #lupus #ehlersdanlossyndrome #cfs #bopo #multiplesclerosis #eds #pots #endometriosis #pcos #depression #anxiety #type1diabetes #chronicfatigue #migraine #wellnessinspiration #wellspo #wellness 👭👬 👭👬 .

🥚🍳🥚🍳 Egg fail, sort of. This started as a Frittata and ended up a scramble. Still delicious! 2 eggs, butter, onion, Genoa salami and cheddar served with broccoli topped with parmesan. Back to bed I go... 😴💤😴💤😴💤😴💤😴 #eggs #protein #homecooking #kcko #weightloss #journey #lifestyle #accountability #keto #ketogenicdiet #ketolife #lowcarbdiet #lowcarb #lchf #healthyfat #wellness #warrior #if #cheese #frittata #scramble #breakfast #dinner #alldaybreakfast #invisibleillness #cfs #fibromyalgia #flare #foodie

3 DAYS until World Tai Chi and Qichong day! Our FREE demonstration and practise workshop will be located at the Flower Gardens on West Park on Tai Chi and Qigong day! (Saturday 27th April) Are we going to see you there? #fibroactive #fibromyalgia #fibromyalgiaawareness #chronicpain #wellness #wellbeing #health #fm #chronicfatiguesyndrome #cfs #derbyshire #5waystowellbeing #westpark #longeaton #taichi #qigong #taichiandqigongday #worldevent #events #community #connect #beactive #services #local #fun

It’s our 30th episode! 🎉 And we couldn’t be more excited than to celebrate with this episode • We have a unique and fun guest today who has such a warm personality. We cover a ton of topics with the insightful Christina from @buenqamino and you won’t want to miss it • • •

I hate it when books break your heart. It's an indescribable misery. I had bought this to read on the plane to Spain. But since that didn't work out, I decided to adopt it as my escape-from-hospital book. But if you know the story from the film, you'll understand that every time Lousia mentions Will, it makes ME miss him 😭💀 I am a mess. But a book-reading mess. So there's that. Also, excuse my manly thumb 🙃 . . . .#chronicmisfitlife #mecfs #cfs #type1diabetes #t1d #myalgicencephalomyelitis #chronicfatiguesyndrome #mecfsawareness #depression #anxiety #health #socialanxiety #fatigue #disability #disabilityawareness #meawareness #cfsawareness #t1diabetes #endometriosis #hospital #hospitalinpatient #aande #migraine #viralmeningitis #meningitis #headache #accidentandemergency #stillme #jojomoyes #mebeforeyou

Went out with our pussy 🤣 So proud of her trying to explore the outside world with ofc our door wide open and us in arms reach 😆 Also love my new hoodie❤😎 #rescuecat #chronicillness #cfs #selfdiagnosis #spoonie #spoonielife #love #bisexuell #bipride #trans #transboy #agender #ftm #dysphoria #battlingmentalillness #agenderpride #transpride #lgbtqpride #lgbt #battlingmentalillness #babyboy #edgy #grunge #friendsfan #relationship #depressedbutwelldressed #gamerboy #gamer

Wtf

Words of wisdom; "we should start going for more walks". This is something my husband and I are constantly saying to each other, as we sit on the couch watching Netflix. We always have an excuse - "oh it's way too hot", "oh it's raining, well go tomorrow". This month we made a goal to actually start going on more walks, no excuses. Even if its just around the block, at least its something. One day, or day one. You decide. 💜

This labor of love is finally done! I’m so pleased. Isn’t she cute?! Woof, y’all. It’s taken me a long, long time to come to terms with being disabled — even using that word as an identity is still pretty new. People have stared at me my whole life. I figured I’d do what I always do: give them some sparkle and keep walking! In the time I’ve had to sit with this cane, I chose to put love into her, so that I can continue to learn how to love myself, exactly as I am, fatigue and pain and dizzy spells and everything. It’s not all roses, but I’m grateful for the ability to still recognize beauty, love, and light when I can. . . . . . #cane #mobilityaid #mobility #rhinestones #diy #sparkly #fancy #spoonie #spoonielife #chronicillness #invisibleillness #pots #potsie #dysautonomia #syringomyelia #raredisease #fatigue #chronicfatigue #chronicpain #arthritis #fibromyalgia #cfs #butyoudontlooksick #invisibledisability #disability #disabled #queer #femme #transgender #lgbt

I don't respond or even read rants made to me in capital letters. I just glance, see it's not favourable and delete. It's odd how upset people get when I caution them, kindly, against giving medical advice. Not suggesting it but giving it forcibly and irresponsibly. You can't tell people to take your advice just because it worked for you. I was told certain things not to do because of advice from three specialists. Then I was advised to do those very things by non medical people. I can't throw my meds away, I'd be dead without my blood thinners. I can't drink lots of water as i am losing blood in my urine and I'm in restricted liquids, which even include how much liquid is in my vegetables ... so even the phrases "drink lots of water" or "make yourself a nice soup" or "eat more veggies" has consequences for me. People unthinkingly give well meaning advice but the ones who grind my gears are the ones who push push push their opinions down the throats of others. These are the dangerous self righteous ones who turn nasty as soon as you point out that they should be more careful. They are not doctors. It's okay to say what worked for you but not okay to tell someone else they should do exactly what you did. We are not medically trained. So to the lady with the caps ... instead of getting angry and nasty about it, why not have a think about some of the dangerous advice you are pushing onto others. As facts not suggestions. As the thing they must do, instead of just sharing your experiences. I was once giving advice too but now I say check with your doctor's. They are the ones who know what they are talking about. #askyourdoctor #qualifiedadvice #advicecanbewrong

Jeg ville bli frisk, men de sa jeg måtte mestre å leve med det..#cfs#me#cronicillness#survivor#bepreswnt#changeyourthoughts Nytt foredrag om dette på bloggen nå. Link i bio☝🏼

Another day, another neurology appointment. 🤕👨‍⚕️ I honestly think I’m going to change neurologists because he doesn’t listen at all and is so quick to dismiss literally everything I say. 🗣 For instance, I know he’s a neurologist, but while I was there, my legs, feet, arms, and hands broke out in a blotchy rash and my toenails turned bluish/purple (2nd & 3rd pictures, no filter - please ignore the state of my toenails ... they’re a result of having to get them cut out and cauterized multiple times as well as being in too much pain to do anything with them) and he said, “Oh I’m not sure.” Then moved on to leaving the room ... without even talking about my brain MRI results, which is what I was there for in the first place. Guess the email saying “normal” was sufficient. 🤷‍♀️ Also, my vision has changed to dull colors/grey with pain behind my eye off and on. AND my voice has been tremoring/changing to raspy/not wanting to coming out ... he completely dismissed it. 💁🏼‍♂️ He is taking me off of #topamax and putting me on #aimovig for my #migraines, though. We just have to wait for insurance to approve it. ⏳💉 In other news, @marloanncavalier stayed perfectly tucked between my legs ... even while the doctor checked my knee reflexes. 😄💜🐶 Now, does anyone know what kind of doctor to go to for blue toenails? 🤨 • • • • #fibromyalgia #fibromyalgiawarrior #fibrowarrior #chronicpain #nervepain #musclepain #jointpain #migraine #chronicmigraine #migraine #migrainewarrior #chronicillness #invisibleillness #depression #chronicfatigue #cfs #essentialtremor #musclespasm #degenerativediscdisease #arthritis #hypermobility #spoonie #spoonielife #servicedog #servicedoggear #sdit #servicedogintraining #multipurposeservicedog

I don’t like asking for help🤷🏼‍♀️. It’s something I’m really bad at doing and there’s two reasons for it; 1. I really don’t like feeling like a burden to the people around me. 2. Asking for help to do basic things makes me feel like I’m losing control over myself which I hate🤦🏼‍♀️. Yesterday I had to ask for help. I haven’t been able to get up from bed in two days which meant I needed food🥗 and I needed to refill my meds💊. Did I get help? Yes, because I have an amazing mom who did it right away, with no more than a “Next time you ask sooner”. I know that she and the other lovely people around me would help me without judging or thinking I’m a burden. And I am so grateful for that. Yet, I still don’t like asking for help. I don’t like the feeling of needing help. I don’t like being the patient. But I do and I am. I need help sometimes and I am a patient a lot of the time. And that’s okay. For now that’s okay. This was gonna be a “it’s okay to ask for help” message, but instead it became a “I don’t like needing help” message. Whoops🤦🏼‍♀️. So here comes the point; no matter how hard it is to believe it yourself, it IS okay to ask for help. It doesn’t make you weak. It means that you’re trying, but that you can’t do it all alone. And that’s okay. Art: @jessrachelsharp

24 de abril, día mundial contra la Meningitis, una infección grave con un alto índice de mortalidad que afecta a las membranas que rodean al cerebro y a la médula espinal. Puede causar importantes daños cerebrales y es mortal en el 50% de los casos no tratados. . . En #medicineshop tú importas👩🏽‍⚕️ #health #chronicpain #chronicpainwarrior #toptags #chronicpainawarness #chronicillness #invisibleillness #chronicpainsurvivor #endurance #survive #invisibleillnessawarness #fatigue #disability #smilethroughthepain #spoonie #spoonielife #chromicfatigue #spoonieproblems #cfs #spooniewarrior #spooniestrong #painsucks #autoimmune #fibromyalgia #painwarrior

Swooooosh. Crop. I should update my artstation. After ref of @itsmartinwallstrom by @morgannorman

Feel so guilty and lost. Having chronic pain and trying to be a mum, a sister, a daughter, a friend is just so hard. All I want to do is get through each day best I can, and i try to stay positive, but sometimes I just can't see it, the light in my heart dims a little & I just need to let myself feel it. I want to be better, & will always fight it, but sometimes on days like this it doesn't seem possible. 😔💔 . . . . #spoonie #relate #tryyourbest #healing #myjourney #thelittlethingsinlife #natureobsessed #skyobsessed #fibromyalgia #cfs #bpd #eupd #relate #painmakesyoustronger #fibromyalgiaawareness #chronicpainawareness #picsart #grateful #anxietyawareness #itsoknottobeok #fightthefear #sendpositivevibes #empath #lightworker #mentalhealthawareness #mentalhealth #chronicpainawareness 💪🏼⚓

Let the research commence! So far google has been my friend. And fb forums for hints, tips & encouragement. But knowledge is power and I want to be fully informed so I can make conscious choices about what I put in my body. This is a pretty hefty bible of a book. Looking forward to feasting on it 🙏🏻#aip #leakygutdiet #glutenfree #adrenalfatigue #cfs #healthyfood #healing #inspiration #knowledge #sarahballantyne #paleo

Both physical and mental health issues can be extremely difficult to deal with. I just want to say that I’m so proud of everyone who suffers with an illness everyday, yet still manages to get up in the morning, put on a brave face and face the world. You are true warriors! I’m so proud of you all 💜 We’re in this together! Also, check out @healthbeme for an amazing new service that’s coming out officially this year, to help support those struggling ✨ #webewarrior

Applications will be opening at 1 PM PST ☀️💘☀️

Laying flat on my couch, watching TV, drinking a cup of tea. Small things to make you feel better 🛋 I think selfcare and mindfulness is important for everyone, even more for spoonies. What's your tip for not-so-good days? What makes you feel better? #invisibleillness #chronicpain #butyoudontlooksick #invisiblyill #fatigue #cfs #chronicfatigue #pots #potssyndrome #tachycardia #hypermobility #hypermobilitysyndrome #spoonie #spoonielife

This spoke to me today. I feel incredibly fortunate to still be among the living💫 The quality of my moments have become so precious. It’s the little things ✨💫🌟#qualityoverquantity #mayaangelou

there are no homeruns when it comes to cleaning up the past the past happened to you. you can't clean it up completely. it's there. And it took time to get to where you're at, it will take time to get better. instead of focusing on getting back to where you were. just focus on your daily care. make daily rituals out of taking care of yourself, working through the mess and finding yourself. dont try to be you from before-the messed up one. find the you that is inside, turn into the person you have inside. a new person. find it. **when you really start trying to right your health. You will meet all kinds of doctors and therapist and extra people. Some idiots to just say goodbye to and some people full of wisdom and time. Turns out my chiropractor has a very similar childhood/homelife as me- but is in a completely different stage of life then I am. Find inspiration when it comes. No matter where it come from.** #fibro #fibromyalgia #fibrowarrior #fibroflare #spoonie #mentalhealthadvocate #chronicpain #cfs #beautifuldisaster #mentalhealthawareness #invisableillness #invisableillnessawareness #pain #anxiety #depression #ptsd #trauma #mentalillnessawareness #mentalillness #bpd #did #cptsd #cptsdrecovery #endthestigma #bipolar #traumasurvivor #butyoudontlooksick #traumarecovery

I just HAD TO share my spoonie sister @tea_spoonie93 video from her @khaleesiscannabombs Dragon passion bath!! So pretty 🐉🐉🐉 I've fast forwarded it a little so you can see the surprise purple middle at the end 💜 all natural non toxic ingredients 100% vegan and cruelty free of course 😉. If anyone has any questions about cbd bath bombs and their benefits just give me a shout 🐉🍁 I personally find them so beneficial for my chronic pain, I rarely have a bath without one now 😂💜🍁 #cbdbathbomb #chronicpain #dragoneggbathbomb

Wow, I’m so amazed that we have grown to over 500 ME/CFS Warriors! Thank you so much! I’m really honored by each and every person who chooses to follow me. Every person that I can connect to helps me feel useful to the world, a major achievement for someone who is housebound and mostly bed-bound.⠀ ⠀ I’m honored have you join me in our journey to cope with our health and find ways to live well limitations. I know how difficult the chronic illness lifestyle is. I strongly believe that the more we come together and support each other, the better all our lives will be.⠀ ⠀ I post every day in honor of our daily struggle with chronic illness. I hope to be your online “friend” that’s makes your burdens easier to carry. I’m not here to make money or sell you anything. I’m here to provide useful tips on how to cope, educate about further resources, offer inspiration, make us all feel less alone in our common struggles and engage us in activism. ⠀ ⠀ I hope to grow this account and reach more people with chronic illness. I’d like to be part of the solutions that will help create change for ME/CFS. Every like and comment makes it more likely that my account will reach more people. Please share my account with people that you know with chronic illness. It’s easy to become disillusioned, disengaged and isolated. I hope that my account provides inspirational connection. It is my dream to reach as many people as possible that need a little validation, hope and useful information. ⠀ ⠀ Please also share this account with the supportive able bodied people around you. I hope that what I share makes it easier for able bodied people to understand the person in their life with chronic illness. ⠀ ⠀ I would also love to know about other Instagram accounts about ME/CFS that you would like to see me collaborate with in the future. ⠀ ⠀ In the future, I will be expanding into regular videos on YouTube. I hope to provide one edited video a month and a livestream Q+A every second and fourth Sunday. ⠀ ⠀ Stay tuned for many exciting things happening here in the future! Together, we are stronger. Together, we can survive anything. Together, we can create solutions for change 💕💪⠀

❤️

This first one hits home HARD. It’s so real. It’s why I loathe showering, and have to save it for the days I have spoons (which isn’t often anymore, honestly). And I have said to Ryan, on more than one occasion, that the single flight of stairs feels like a mountain, and when I reach the top, I have to take a minute or two, every time, just to collect myself because of how difficult and challenging it is. It’s not fair. And maybe it’s the lack of sleep (I didn’t sleep again last night, which has caused worsened pain today) getting to me, but it’s so hard to see the silver lining some days. The world just feels too big and every tiny task feels so overwhelming. And then I see something that says how stress can worsen my conditions, so people should just try to reduce stress! No big deal! ...HOW DO I REDUCE STRESS WHEN EVERY TINY THING IS AN INSURMOUNTABLE MOUNTAIN? I’m just so tired. I don’t want to do it anymore. But just like this second photo says, I have thought that so many times...and yet I’m still here. Somehow, I manage to push through. It’s amazing, what our bodies and minds are actually capable of doing to get us through things. Also, I know there are people much worse off than me. I am grateful I CAN still walk without assistance most times (I won’t go into my dark fears of how that will change in the future, given how drastically my condition has worsened over the past few years). So, I’m medicating myself today and going to try to tackle the million errands I have to run before picking up the kids and running them around to scouts, etc. Sorry for the rant again; thank you to everyone who reads these whiny posts, and who is here for me regardless, and who supports me even when you may not understand. It means everything to me, when I feel so completely and utterly alone. #spoonie #chronicillness #chronicpain #chronicfatigue #invisibleillness #invisibledisability #invisibledisease #cfs #cfsme #mecfs #insomnia

⚜️ Muitíssimo boa tarde!!! ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ 🎧 Um pouco mais do trabalho do PONTIFEXX (@pontifexx,) que estará conosco no Coffe Break, por uma causa nobre!! ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀🎟️ Se ainda não garantiu seu ingresso, corre que o primeiro lote encerra hoje às 19h!! ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ #cfs #congressofilantrópicodesaúde #conhecimento #projetosocial #11/05/2019 #oevento #cfs #façaadiferença #habitat

Today started with a gentle 2.5 mile jog with #cocothecockapoo and @benja83 at Heartwood forest 🌳 to check out the bluebells 😍 Before I got #cfs I would have pushed myself to be running further or faster everytime. But now I just do a slow and steady jog every now and then and stop to admire the view as I go (👉🏻 swipe to see that view and those bluebells) but it still brings me such joy. People often ask me about exercising with #cfs and so I finally got round to writing a blog post on the topic...link in bio. I procrastinated on it for a while because I’m not a personal trainer but I hope by sharing my experience of returning to exercise after being virtually bed-bound with CFS it will inspire you to believe you can do it too! It’s a long post but I wanted to make sure I gave you as much insight as possible. I hope you find it helpful and if you do...please like and share this post. If you have any questions please feel free to comment below or DM me but please note I am not a qualified fitness professional so can only share advice from my experience! #eatbreathebelieve #healthy #healthyliving #wellbeing #healthylifestyle #nutritionist #stalbansnutritionist #keepingitsimple #healthylife #nourishedlife #plantbasedliving #fitness #exercise #chronicillness #chronicfatiguesyndrome #recovery #cfsrecovery #intentionalliving #motivation #inspiration #inspiringchange #getmotivated #balance #nature #happylife #happy

When your fam brings you flowers because you're down and in so much pain💐🌹🌼🌻🌸 #spring #springtime #spring2019 #spoonie #spoonielife #spoonies #chronicpain #chronicillnesslife #chronicillness #chronicdisease #fibromyalgia #fibro #disability #disabled #cfs

I overdid it a bit today, but I wanted to see the pretty flowers so badly. The rhododendrons have come out and are looking great! Now I'll be sleeping off the after effects for the next few days... #2019inpictures #flowers #walking #parkwalk #disability #cfs #disabledhikers #unlikelyhiker

Palestra com a Tenente Pollyanna, fisioterapeuta, sobre a ”Importância em manter-se ativo”. E o Sr Cristian palestrou sobre “Estratégias nutricionais na prática de atividade física”. O comando da escola agradece aos palestrantes a presença e os conhecimentos passados. . . #policiamilitar #pmmg #efaspmmg #cfs #casp #cefs #rotam #bpchoque #acimadetudobrasil #pmmgforcaehonra #missao #visao #valores #policiadobrasil #soupolicial #policiadopovo #militares #cursodeformacao #melhorpolicia #gloriosa

Buenas Tardes Gente 👋 _ Empezamos a subir las fotos de algunos autos que se hicieron presentes en el encuentro de #vaconestilo4homenajeaeveesonderman . Cabe aclarar que no se le saco a todos los autos por que era impresionante la cantidad que estuvieron presentes y seguían llegando...solo nuestro Ph: @gaby_zura tiro por aporte mientras ivan viendo e disfrutando del encuentro. _ 🚘: ~ _ 📸:@gaby_zura _ Prohibida la edición/recorte de las fotos o la firma. Permitida la difusión a traves de la opción "Directa". GZ Ph todos los derechos reservados - Ley 11.723/235 🚫 _ Pd: Etiqueten a los dueños si conocen sus autos. Gracias! _ #centenariofierros #cfs #cfsracing #vaconestilo4homenajeaeveesonderman #vaconestilo4 #berlina #fiat128 #fiat #fiat128berlina #iava #abarth

Ahhhh pain mgmt. . . . . . . . #chronicpain #cfs/me #cerebralpalsy #extravertebrae

Här springer hon...lilla mammi, med dammsugaren i högsta hugg före varje pass, för att jag ska kunna spara energi till att ha yoga! Oerhört tacksam för att ni finns, mamma och pappa! ❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️ #världensbästaföräldrar - - - #holiyoga #yogabyme #yoga #västerås #meditation #psykologi #andning #vila #återhämtning #läkning #utmattningssyndrom #sjukskriven #utmattning #fibromyalgi #fibro #spooning #migrän #utmattningsdepression #mecfs #cfs #sömn #smärta #ångest #psykiskohälsa #psykiskhälsa #hälsa #måbra #alltblirbra 🧡

On this beautiful snowy Saturday, I can't help but get excited for Christmas soon approaching and want to make sure my immune system is strong and ready to enjoy the festivities. . 🎄 My cup of tea today has Echinacea and Dandelion. A blend I really enjoy, that's both nourishing for the whole system, while gently cleansing and toning the liver and kidneys. . 👩🏻‍🔬 Echinacea boosts the body's first line of defence against many illnesses while helping the body restore white blood cells. Dandelion root and leaves help replenish and rejuvenate the whole body through the liver and kidneys. . 🌿 These two combined can work magic for your body when taken regularly after poor diets, processed foods and an increase in the consumption of toxins, which can weaken the immune system and make it more susceptible to catch a cold or other sickness, especially around the holidays. . 🤶🏼 Stay cozy, stay safe & stay healthy this weekend! . 🎄❄️ Follow @tearapeutic for lifestyle tips, teas and herbal remedies. . . • • • • • • #chronicillness #chronicpain #spoonie #invisibleillness #fibromyalgia #chronicfatigue #gastroparesis #spoonielife #lupus #cfs #lymedisease #autoimmune #epilepsy #endometriosis #dysautonomia #chronicallyill #ehlersdanlossyndrome #fibro #disability #butyoudontlooksick #cysticfibrosis #autoimmunedisease #pots #ehlersdanlos #posturalorthostatictachycardiasyndrome #fatigue #crohns #multiplesclerosis #migraine #foodismedicine

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