#autoimmunedisease

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Exactly. That's why we say "I'm fine". #menwithfibromyalgia #fibromyalgia #autoimmunedisease #chronicillness
Ileostomy since 2017and proud. No shame here. Ostomy and still beautiful. Enjoy the days when I'm strong and feel good💖🗻🌠 #ostomates #ileostomy #chrons #fibromyalgia #sickinside #smileoutside #tumalooregon #noshame #autoimmunedisease
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Something to think about on this Sunday afternoon!!
Today we slow cooked a pork shoulder for 10 hours to make delicious, paleo pulled pork 🐷😋 It’s nice to be back home in our own kitchen after our time in Florida 🏡😍 ~ #paleo #paleodiet #glutenfree #dairyfree #refinedsugarfree #pulledpork #dinner #homecooking #homesweethome #vancouver #autoimmunedisease #multiplesclerosisfighter #hashimotosdisease
I’m “Indulging” in gluten for the next couple of weeks for an upcoming endoscopy I have to get. Indulging is in quotes because I feel bloated and scatter brained and all around not great. But I’m making the most of this. Dos XX with lime and salt. 🍺#glutenchallenge #autoimmunedisease #celiacdisease
Back at it. 💪🏻 Recovery from spinal surgery✔️Recovery from chronic illness, that’s next. I’d scale anything just a few years ago with superhuman strength & endurance. 💪🏻 Gradually I deteriorated, unable to participate in things I enjoyed, and at my worst, landed in bed for months. Most days felt like a gnarly flu coupled with horrific reactions (thanks, MCAD) shakes👎🏻body temp fluctuations👎🏻digestive issues👎🏻 brain fog👎🏻 dizzy spells👎🏻and much more. Today, no more bed. Today, nada reactions. Today, learning how to manage this pain in the ass called MCAD. If you’re dealing with chronic illness PLEASE change your diet.🙏🏻 BE a detective. READ every label. If it sounds funny, DON’T eat it. Pathogens love that shit.🦠🌻 • • • #lifeexperience #workout #eatclean #scoliosis #spinalsurgery #cdrods #chronicillness #chronicfatigue #movingforward #justdoit #faith #healthylifestyle #patience #time #recovery #believe #trust #motivation #lyme #hashimotos #autoimmune #autoimmunedisease #chronicdisease #lymedontkillmyvibe #fit #fitness #body #bodypositive #strength #comeback
Infusion yesterday morning. It was literal hell. My Veins are shot. It Took her 30 minutes to draw 2 tubes of blood from the Iv I had. So next week I see primary to talk about inserting a port 🤞🏻 #Lupus #lupusflare #lupuswarrior #lupusawareness #spoonies #spoonie #spooniesunite #spoonielife #fightlikeagirl #theglamorousspoonie #autoimmunedisease #degenerativediscdisease #degenerativebonedisease #degenerativearthritis #bonedisease #interstitialcystitis #gastroparesis #fibromyalgia #chronicpain #chronicpainwarrior #chronicillness #survivor
Yes. 💪🏼
Just look at this gorgeous cake my wonderful hubby @haskinje made me for my birthday!!! I mean, #swoon 😍😍😍 Murph is ready for a piece! 😂(delicious recipe from the super talented #abeautifulplate ) . Another beautiful and messy year spent living this life. So much to celebrate and so much to be grateful for and SOOO many lessons offered. I’ve learned and re-learned that...creating joy takes conscious effort, sisterhood heals beyond measure, I can break and heal many times over, curiosity is essential to my being, growth is often painful, strength takes so many forms, the darkness shows me the light, my illness informs every aspect of my life and that is okay, celebrating the baby steps is just as valuable as celebrating the giant leaps, mom was right - making the bed changes everything, the only person who can truly sign my permission slip is me, illness is a relentless but beautiful teacher, asking for help is not failure, I can feel totally opposite emotions at the same time and both are valid, I am worthy simply because I am a human who exists, I am enough, and I CAN do this. I did it you guys! I made it another year. For that I am tremendously grateful. To all of those who have showed me love and offered me support this past year I have such deep gratitude for you. ♥️🙏🏼♥️
Love this quote from @dollyparton. If you haven’t watched Dumplin, it’s a must watch!!
Party was a success. Here’s a picture from before the party. I’m currently fighting severe pain, hives and migraine trying to rear it’s ugly head. Edibles, Tylenol, Motrin, Flexeral, Zofran, tens, essential oils, heating pad, ZENBand, ZENTones and sleep. . . . . . . #mastcellactivation #fibromyalgia #arthritis #hasimotosdisease #asthma #chronicurticaria #angioedema #mutiplechemicalsensitivities #degenerativediscdisease #migraine #autoimmunedisease #adhd #ptsd #majordepressivedisorder #invisibleillness #chronicpain #chronicillness #idontlooksick #autoimmunewarrior #fibromyalgiawarrior #hasimotoswarrior #spoonie #multiplechemicalsensitivityawareness #chronicillnessawareness #invisibleillnessawareness
Up almost 20 pounds. 90 pounds to 107. Never thought I’d say this, but YAY! I gained almost 20 lbs. My numbers look good on my blood tests, my hair is growing in, I have energy again. #remission #nevergiveup #autoimmunedisease #carnivore #shortgut #youarewhatyoueat #staycalmandrelax
This is the life a a chronically ill person. No one would want to take all these medications if they didn’t have to. We wouldn’t fake this for attention and this isn’t all in our heads. Left side is evening meds. Right side is morning meds - missing one because I am out and am waiting on a deposit to go through to be able to get a refill. The larger eye drop in the night time side I use several times a day due to eye dryness caused by Sjögrens Syndrome. Not pictured are the calcium pills I have to take 4 hours after my morning meds, but 4 hours before my evening meds so they don’t bind to some of my other medications and make them ineffective. This also doesn’t show the mouthwashes I have to use several times a day, the special gums, and the special mints I have to use because of dry mouth because of Sjögrens Syndrome. Can we talk about the few essential oils I’m not reactive to that I use for chronic migraines, gastrointestinal issues, and chronic pain due to Mast Cell Activation Syndrome, Ehlers Danlos Syndrome and Sjögrens Syndrome? And the loads of Gatorade and Lyteshow Electrolyte water I drink for issues from Euler Danlos Syndrome (it helps keep the small vessels open in the extremities according to my geneticist and everything working right with my heart) and possibly Postural Orthostatic Tachycardia Syndrome. #sjögrens #autoimmunedisease #invisibleillness #chronicillness #spoonie #butyoudontlooksick #chronicpain #ehlersdanlossyndrome #eds #mcas #mastcellactivationsyndrome #posturalorthostatictachycardiasyndrome #pots #dystautonomia #chronicmigraine
This is the life a a chronically ill person. No one would want to take all these medications if they didn’t have to. We wouldn’t fake this for attention and this isn’t all in our heads. Left side is evening meds. Right side is morning meds - missing one because I am out and am waiting on a deposit to go through to be able to get a refill. The larger eye drop in the night time side I use several times a day due to eye dryness caused by Sjögrens Syndrome. Not pictured are the calcium pills I have to take 4 hours after my morning meds, but 4 hours before my evening meds so they don’t bind to some of my other medications and make them ineffective. This also doesn’t show the mouthwashes I have to use several times a day, the special gums, and the special mints I have to use because of dry mouth because of Sjögrens Syndrome. Can we talk about the few essential oils I’m not reactive to that I use for chronic migraines, gastrointestinal issues, and chronic pain due to Mast Cell Activation Syndrome, Ehlers Danlos Syndrome and Sjögrens Syndrome? And the loads of Gatorade and Lyteshow Electrolyte water I drink for issues from Euler Danlos Syndrome (it helps keep the small vessels open in the extremities according to my geneticist and everything working right with my heart) and possibly Postural Orthostatic Tachycardia Syndrome. #sjögrens #autoimmunedisease #invisibleillness #chronicillness #spoonie #butyoudontlooksick #chronicpain #ehlersdanlossyndrome #eds #mcas #mastcellactivationsyndrome #posturalorthostatictachycardiasyndrome #pots #dystautonomia #chronicmigraine
I love my forever puppy. She has her good days and her bad days. And I know she probably wont grow old but I'll love her with all my heart until the pain becomes too much for her:( #specialneedsdog #autoimmunedisease #raggle #beagleratterrier #delilahdog #adoptdontshop 🐾
Had a fabulous time tonight at #Rawhide with the #Family ! There was a #savechristmas activity where you had to search for Santa’s lantern to save the holiday & my 4 year old grandson found it!! They announced his name over the speaker & everyone cheered him on! He got a photo with Santa! It was amazing!! It was the coolest thing, he was so excited 😆. It was nice & chilly & we all had a great time especially the kids. Precious memories 😊♥️ There’s me at the end being all happy & stuff 😄 Goodnight & prayers for a low pain, low sickie night. #familynight #25daysofchristmasactivities #xmas #christmas #familytime #lovemyfamily #christmastreelighting #snow #justme #decorations #this #sotrue #mytruth #myspoonielife #spoonie #santaclaus #myspooniejourney #chronicillness #chronicpain #chronicfatigue #truth #purpleness #invisibleillness #autoimmunedisease #spoonielife #spoonietruth #autoimmuneillnesses 💜🌻🌷 🎄🎅♥️
@tessnboots and I are wrapping up Smokey and Zephyr’s unfinished bucket lists this weekend with a trip to #SanDiego ! 🐾☀️ . . To Smokey: I’m sorry you and Zeph couldn’t make it here in life but I’m glad we got to bring you here in spirit. . . #caninelymphomasucks #bucketlist #dogmoms #california #coronadobeach #hodads #vacation #beach #sand #caninelymphoma #autoimmunedisease #cancer
Who else has to buy fake Christmas trees because they're allergic to real ones? . . Doesn't make it any less beautiful thankfully! I think next year I'll put a real one on the front porch so we get the fun of cutting one down and smelling fresh pine! 🎄
Stay positive 😊😇⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀ The Health Chef 👨‍🍳 Share your pic and a heathy dish recipe and get a chance to be featured on our page 😊⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ #thehealthchef #healthyeating #invisibledisease #chef #diet #msdiet #mshappydiet #recipes #cook #cooking #awareness #mssymptoms #msday #multiplesclerosis #invisibleillness #ms #fatigue #insomnia #positivevibes #positivequotes #positiveattitude #msfatigue #symptoms #msday #fibromyalgia #chronicpain #chronicillness #mswarrior #curemultiplesclerosis #msawareness #mssymptoms #autoimmunedisease #insomnia
This right here.... this DESTROYS me to no end. To hear my baby cry and want it all to end. He's tired of feeling like this, wants to be normal and do all the things kids do. I'd do anything to trade him places. No child should have to feel this way all day, every day. #pandasdisorder #pandassucks #pandas #pandassyndrome #autoimmunedisease #chronicallyill #lymediseasewarrior #lymedisease
Sunday Scenes 😍 ——————————————————————–– Follow: @lifeinafastrack #lift #lifeinaftrack #lifeinafastrack ———————————————————————— Pic: @nissan_sky_net Owner: @r35_cory #gtr #nissan #skyline #legend #godzilla #paulwalker #jdmlife #rb30 #boostedlife #gtrr35 #boosted #nissanskyline #r34gtr ———————————————————————— #autoenthusiasthub #drivelikeyoustoleit #autoimmunedisease #followforfollow #instagram #likeforlike #follow4follow #like4like #likeforfollow #follow
THANK YOU to all of you who DM'd me lately asking questions! . I flipped the name on this account, created a new one for my artwork (@marinleeart ), and am mentally preparing for a lot of changes over the upcoming months. . Stage 3 Adrenal Failure is what I'm working through, with a Functional Medicine Doctor to repair. . What is this? The short version is all of my hormones are outta whack. . My cortisol levels are backwards. When normal people are awake my body can't produce enough energy to be awake. Hello caffeine. . When I should be tired and ready to sleep, my body is producing excess energy (cortisol) and I'm wide awake. . I don't know what the months ahead will bring but I know one thing is certain. I've been preparing for this for a while, I'm ready to kick ass, and I appreciate all of YOU who continue to follow along this journey with me! . #marinleefitness #fitnessfashionista #fitnesslifestyles #squatbooty #legday 🍑 #functionalbodybuilding #hiitcardioworkout #carbcycle #flexiblediet #100to0 #duespaid #girlswholiftheavyshit #lululemonaddict #iam1stphorm #bouldershoulders #gymaddiction #autoimmunedisease #fitnessfun #fitnessjourney #macrolifestyle #deadliftday #dothework #wintheday #legionofboom #teammeat #onlyus #onedayatatime #adrenalfatiguerecovery
Ich wünsche Dir einen schönen, aber vor allen Dingen besinnlichen 3. Advent.⠀⠀⠀⠀⠀⠀⠀⠀⠀ Wie besinnlich wirklich geht? Vertrau auf das Ying und Yang Prinzip.⠀⠀⠀⠀⠀⠀⠀⠀⠀ Meine neue Podcastfolge kannts Du wie immer über die bekannten Portale hören (Link in Bio) ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ #rheuma #rheumatoidarthritis #chronicdisease #painfree #alternativemedicine #mentaltraining #naturally #autoimmunedisease #autoimmune #Rheumacoach #verenafassbender #rheumatoid #rheumatology #rheumatism #rheumatic #rheumatoidarthritisproblems #rheumaheilen #autoimmuncoach #nomedicine #ganzheitlich #Hannover #gelenkliebe #energyhealingart #Mallorca #Köln #authentic #weihnachten #Lüdenscheid #podcast
Asthma, arthritis, swollen lymph nodes and tonsils, rhino sinusitis...light headed and working on a lot these past few days. . After one more task I’m off to bed and hope I sleep for once without insomnia. . . . . . . . . #eclecticawareness #awareness #saturdaynight #sickdays #sotired #exhausted #chronicfatiguesyndrome #cfs #insomnia #insomniac #like #likes #follow #needsleep #longday #arthrtis #chronicpain #autoimmunedisease #spoonie #spoonielife
❄️Happy December everyone! ☃️I know I’m a few weeks late; tbh I’m still catching up on October and November! Being admitted in the hospital really took a lot of time from me. Since that oh so fun hospital stay, my family and I have been having to relearn and adjust to our new “normal”. I kind of unintentionally took a month long hiatus from being active on here. I just didn’t feel very motivated or if I’m being completely honest by the time I faced my daily struggles and even small accomplishments, I just didn’t have enough energy left in me to post. My account started to feel like a chore, and a bad reminder of my reality; and that’s the complete opposite of what it was intended for! So I took a bit of a mental break and have really been focusing on myself and trying to recover as much as I possibly can; so now when I post it will be a reminder of how much I’ve been through and have overcome! So these last couple months have definitely been challenging! It’s been nothing but trial and error trying to figure out what meds work and which don’t. My days have consisted of ~Finally finding meds that work, only for them to cause negative side effects. Dealing with disappointment from doctors who are supposed to listen to you. Fighting off several infections and having allergic reactions to antibiotics that I’ve never had an issue with before! Several procedures. And my favorite, the endless amount of normal people germs making their way into my crappy immune system over and over again is really fun.😷~ It’s been very difficult mental health wise. My depression and anxiety have been in full swing. Just trying to manage and stay on top of everything; also having to rely on other people for everything is really hard,especially since I’ve always been very independent. So as you can see my body has been very busy just trying to cope with all these illnesses attacking my body, and my brain is trying to keep up. But for the first time in awhile I’m feeling just a tiny bit hopeful for my future! Now for positive news! ⬇️cont. in comments.❄️
Christmas Party 4 days until our TIREDGIRL Christmas Party starts. We are hosting an online party for women with chronic illness to get together over this holiday season. Sharing an understanding of how hard it can be to navigate this busy time where you may be feeling overwhelmed by socializing or expectations from the growing demands of 'The Perfect Christmas'. Here, we can come together and celebrate in our own way. Gentle. Supportive. In bed. In our own time and in our own voice. Our TIREDGIRL Christmas Party runs over Christmas and New Years and we want to celebrate with you! We'll talk about all things Christmassy as well as offer each other support and friendship. 20th December - 3rd January. Tag a TIREDGIRL friend to invite her to the party. Become a member on our website for free to join in on everything we do, and have fun with a beautiful community of friends this holiday season.
It’s been a long week... a very physically (and subsequently mentally) exhausting. A rheumatologist appointment earlier this week that included the words “that is an unfortunate coincidence” (when referencing my gallbladder that died, appendix that leaked, giant tonsils and Fallopian tube that clogged and filled with 7 lbs of fluid), and I had really bad abdominal pain for ten hours so Matt took me to the ER. I have a kidney stone and severely inflamed mucus lining inside all my intestines and gastritis (inflamed stomach and esophagus). *sigh* so now I’m home on a clear liquid diet waiting to call my primary care doc Monday morning. It’s hard. It’s hard when you work so hard to eat right and treat your body well. I’ve been on strict AIP since April, and I’ve seen some improvement, but I keep having massive setbacks. On days (or weeks) like this, it is easier to give into the depression. To believe that my life will be one health disaster after another. But I refuse to believe that this is all there is. So tonight I am sipping my bone broth so I can take some CBD oil, snuggled up with my dog and heated blanket, and choosing to believe that God has a plan in all of this that brings Him glory. . . . . . #aip #kidneystone #donutcare #bonebroth #cbdoil #cbd #autoimmuneprotocol #autoimmunedisease #chronicinflammation #longweek #gastritis #clearliquiddiet #Godisgood #thesunwillcomeuptomorrow #thestruggleisreal
Speaking of #coffee Our coffee has been causing a stir. People with pain that the oil has only begin to touch, people with the need for clairity of thought and other things are reporting that they can't believe the results. This coffee is the perfect Christmas gift along with keto creamer for anyone who has bad chronic pain or other issues. THC free but with good for you CBDs. #coffeelover #momlife #parenthood #yum #choices #wellness #health #keto #ketodiet #massagetherapist #yogainstructor #gratitude #migraines #scoliosis #hashimotosdisease #autoimmunedisease #chronicpain #chooseyou
New blog up guys!!! All about what its like to live with 3 different auto immune disorders!! Check it out and let me know what you think! Blogwithkas.blogspot.com #spoonie #chronicillnesslife #autoimmunedisease #youvegotthis
Do you make your own milk? I’ve been making mine for nearly a year now. While I have purchased ready-made nut milks from the store in a pinch, here is why I don’t make it a habit: 🥛 - Gums . There are many types of gums out there and they are all mostly used as thickening agents. If you have gut issues — STAY AWAY. Guar gum can cause increased gas, bloating, diarrhea, and loose stools. Xanthan gum can swell the intestines which can cause symptoms associated with IBS. It has been shown by studies that locust bean gum may compromise the absorption of nutrients like iron, calcium, and zinc. - Carrageenan. I stay away from this ingredient at all costs. It has been attributed to ulceration and inflammation. It is used as a thickening agent but has no nutritional benefits. - Sugar. If you suffer from any kind of chronic gut distress and inflammation you have to cut sugar out. 🥛 My favorite nut milk to make is a mix of almonds and cashews. The cashews make the milk slightly thicker (not by much admittedly) but as a girl who used to only drink whole milk, I appreciate it.
It's been a long week. A long month, hell a long year! It's like building blocks that you just keep stacking up and just waiting for them to just fall. 2019 has got to have something better, maybe no more new diagnosis! Anyway on my husband's second pair of socks with in one month! What.....that's something new for me! Knitting is the only thing keeping me sane. #knittingismyyoga #knittersofinstagram #knittersofig #igknitters #instaknit #scleroderma #autoimmunedisease #chronicillness
Saturday V*I*B*E*S ☀️ Key west tee shirts 👚 Summer dreams, sunrises & sunsets 🌅 Goal smashing sesh ✍🏻📚 2019 Plan 🗓👩🏼‍💻 Self Care Schedules 🧘‍♀️📕😴 Level 🆙 on Fitness 🏃‍♀️ More Plant Based Meals 🌱 NEW Mindset Shifts 🧠💡 Set Course Schedule for yr/$📚 Travel More 🎪✈️ Play Harder 🎡⛱ Have you planned out your Mindset, Nutrition and Fitness Goals For 2019? Don’t forget to fit in Self Care and PLAY. What is the first thing you are doing differently next year? 🏃‍♀️🏃‍♀️🏃‍♀️🧘‍♀️🥋🏋🏼‍♀️🤸🏼‍♀️🏄‍♀️🚴‍♀️ #fitlife #yoga #2019goals #crushgoals #creativeplanning #planfor2019 #fierceAF #badassery #bossup #likeaboss #entrepreneur #girlgang #girlboss #fitnessfreak #autoimmune #successisinevitable #loveyourlife #saturdayvibes #liftheavy #down35 #thebestversionofher #jenbaucomtv
Is this you? Do you want to get out of the endless trap of getting nowhere? I can help you. Im already helping others achieve their goals. Reach out to me with a comment or message and let me help you😁 www.livelovehealthyliving.com #livelovehealthyliving #letmehelpyou #letushelpyou #youcandothis #liveyourlife #thyroidproblem #fibromyalgia #diabetes #autoimmunedisease #guthealth #weightlosstransformation #weightlossjourney #wellness #wellnesscoach #lifestyle #changeyourlife #chnageyourself #wellnesswarrior #30daychallenge #healthyliving #liveclean #donnacollins #paulfrichot
I want to apologize for not posting for a little while recently. I've been going thru some things in my personal life and will hopefully be able to share about it soon, once I know exactly what's going on that is... So much LOVE to all of you for not ditching! 😘 And I hope your all doing fan-freakin-tastic! #gottastaystrong #positivevibes #health #fitness #illness #anxiety #depression #autoimmunedisease #gravesdisease #addictionsupport #selfimprovement #selflove #selfcare #supportforpeoplewithadiseaseoraddiction #YESWEAREALLBEAUTIFUL
I grabbed the wrong ginger snap cookies and I’m paying for it now #epicfail #notglutenfree #everythinghurts #autoimmunedisease #mssucks
Trying to be better about practicing what I preach! At the gym on a Saturday night 💪🏽 My favorite cardio routine is stairmaster followed by elliptical. It’s relatively low impact and gets my heart rate up! The American Heart Association recommends exercise that raises your heart rate to target, which is 50-85% of your maximum heart rate (220-age) for at least 150 minutes per week. ❤️🏋🏻‍♀️ . Did you know that people with rheumatoid arthritis have a 1.5 to 2 times higher risk of heart disease, which is comparable to the risk we see with type 2 diabetes? This is due to the higher level of inflammation in the body that can damage blood vessels in the heart just as it can damage joints. More motivation to live a healthy lifestyle with healthy diet and regular exercise! 💪🏽 . . . . . . #exercise #cardio #healthy #goldsgym #gym #workout #nutrition #saturday #lifestyle #health #medicine #doctor #md #arthritis #pain #inflammation #ra #rawarrior #autoimmunedisease #spoonie #functionaltraining #instahealth
I saw this post the other day on a friends timeline and couldn’t wrap my head around the fact that this crazy life of ours has reached a whole new level around here. Not just for me, but for my little girl too. Here I am picking up our monthly supply of thyroid meds and having to go to 2 separate pharmacy’s because neither of them can seem to keep their meds stocked up. I was taken back at how much I used to spend on just myself alone when I never really stopped to understand and educate myself on my own thyroid disease. I was always dishing out money like crazy. “Doctors say I will never get better or go into remission...I am not giving up, but I want to make others aware. A nap won't help. I am not lazy. I am on meds. I struggle with pain, mobility issues and fatigue every day. The most frustrating part is people look at me and say "It can't be that bad; you look fine." Despite the fact that my body is experiencing excruciating pain all over. I apologize if I miss events that I would love to attend. One day you'll understand my daily struggles. This disease affects me physically, mentally, and emotionally. I need your support, not your judgment. I'm watching the ones who will take the time to read this post to the end." Want to know a little secret that helped me from having to make those unnecessary trips to the endocrinologist to get meds adjusted? It’s this community of people I’ve found through this little thing called FB/IG that have helped me find the healthiest ways to live for today! It’s this community of people that I’ve found that I can ask questions, find answers, and feel like I’m apart of the solution instead of the problem. It’s this community of people who will always be there to uplift me when I feel like my world is crashing down on me when I have no where else to turn. Sure, me and my little girl have an autoimmune disease... but does that control who we are... not a chance! We are #fearlesslyliving with Hashimoto’s! We are fighting the fluff together! #fightthefluff #foodisfuel #hashimotoswarrior #focusonyourself #hashimotosthyroiditis #wearehashimotoswarriors #thyroidproblems #autoimmunedisease #issues #fitmom #fitmum #thyroidkid
Trying out the new food dehydrator! First up was cucumber chips and they came out delicious! I cut them on the mandolin about 1/8 inch thick, added onion powder and sea salt and dried them for about 5 hours, rotating trays. I bought a round roast for tomorrow and will add coconut aminos, apple cider vinegar and some garlic, onion powder and sea salt to try an AIP beef jerky. What is your favorite use for your dehydrator? Please share your recipes! #aip #aiprecipes #aipdiet #aippaleo #dehydrator #dehydratorrecipes #dehydratorlove #beefjerky #beefjerkytime #cucumberchips 🥒 #autoimmunedisease #rheumatoidarthritis
Clearly we kicked butt at the photo booth. 📸 Baby bear’s first movie on the “BIG TV” tonight. She ate approximately 3 pounds of extra buttery popcorn, 1382 pieces of candy and a half gallon of Coke. You’ll likely get a contact sugar high if you’re anywhere near her for the next week but she declared it the best night ever. Love getting to spend these special moments with her. ❤️
We have been documenting his journey on Facebook and just started his page on here. Follow us on both accounts 💚🐼 FB link in bio 💚🐼 #pandasdisorder #pandassucks #pandas #pandassyndrome #autoimmunedisease #ocd #tics #anxiety #strepthroat #lymediseasewarrior #lymedisease #lyme #lymedontkillmyvibe #chronicallyill
It used to be easy for me to relax and check out, before I had a baby and my responsibilities quadrupled. I tried to relax in the infrared sauna at the gym for 20 minutes, since I’ve been dealing with some autoimmune flare-ups, and didn’t last 5 minutes before I started checking my to-do list. But at least I got a decent sweat out of it. #babysteps #sauna #infaredsauna @sunlightensaunas @sunlightenwellness.rooms #sweatitout #autoimmunedisease #health #mommybrain #relax #unwind #metime #distracted
Beyond thrilled that I took some time off work to head out to Disneyland for some much needed family time ❤ - We've been trying to get to the parks for weeks. But with my crazy insane work schedule, it wasn't possible till today. - The holidays are my favorite time of the year....the decor and trees are stunning! ➡️ swipe right to see what I'm talking about.
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Thirsty Thursday (On a Friday) Research. @rising_springs amazingly gifted me a box of their water today. Had an incredible chat with their lovely leading lady, and am excited to learn more about this company. Eagerly anticipating my first glass tomorrow! #thirstythursday #risingresearch #wellnesssleuth #staytuned #listeningoverlattes #decafcanbedelicous #coffeeandwater #irony #dehydration #hydration #coolcompany #friendlyfun #health #wellness #healthcoaching #coffeeshop #serendipidty #fitness #exercise #beauty #yoga #paleo #vegan #longevity #vitality #lymedisease #autoimmunedisease #chronicillness #lymewarrior #awareness
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