a true beauty
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Because of my reactions, I can no longer touch my cat without reacting, but I can still adore her cute face!! I’ve been having several harsh reactions again, but at least I can still tolerate Kate Farms. All these reactions are making me feel horrible, so I’m not looking forward to the draining week ahead. On the bright side, I’m seeing my pediatrician on Tuesday to discuss next steps. 💪 #ehlersdanlos #ehlersdanlossyndrome #eds #edszebra #zebrastrong #zebrawarrior #edsstrong #edswarrior #pots #posturalorthostatictachycardiasyndrome #potsstrong #potswarrior #allergies #allergicreactions #allergyissues #allergyprobs #elecare #mcas ??
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A little piece of wisdom to start out the week. This is a lesson that I’m trying to learn. Who is to say that a “different” life is not a meaningful life?
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Two days, two dogs, two amazing friends 💜 how’d I get so lucky? @_rhia.nnon_ and service doggo Wilson gave lots of love and doggo sneezes in my face 😂 And @sfausher10 and foxy doggo duke gave me so many laughs as he sat his naught butt in her face 😂.💙 . . . #friendsforever #dogsofinstagram #servicedog #bestfriends #doggos #spooniefriends #spooniefamily #dysautonomia #pots #posturalorthostatictachycardiasyndrome #inappropriatesinustachycardia #ehl#ehlersdanlosrome #ehlersdanlos #eds #rheumatoidarthritis #rheumatoiddisease #gastroparesis #autoimmunedisease #mastcellactivationdisorder #invisibleillness #chronicillness #butyoudontlooksick #fightlikeawarrior #spoonielife #choosejoy
37 0
Même si la vie n'est pas toujours rose,qu'il te faut renoncer à ta vie d'avant ,que la peur traverse tout ton corps et que toutes ces opérations et rééducation son très dur et épuisante il faut continuer à y croire,continuer à ce battre et croire en la recherche #ehlersdanlos #doublefracture #scoliotiquethoracolombaire ainsi que d autre soucis liés à la maladie
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Day off means errands must be run so I take my #servicedog Bossie with me to help keep me in check. Bad pain day and new shit heart medication means he's kept close eyes on me all day because he's the best #pupper so hopefully these errands don't take too long. #spoonie #chronicallyill #chronicillness #invisibleillness #butyoudontlooksick #servicepitt #pitbull #pitty #amstaff #pale #lyme #lymedisease #eds #ehlersdanlos #ist #sinustachycardia #piercings #whitehair #grannyhair
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I use my hands. A lot. Outtake from the photoshoot on Baltimore last weekend 📷
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I melt into the people around me. I form my identity from them, I build it upon them. That seems unsustainable, possibly unhealthy; I need to rest in who I am without them. And I have, to a large degree. But isn’t that ... normal? You move to a new city: you see new things, go new places, meet new people. And it changes you (as well it should, as well it must). It's a new mirror. Identity is just the mass that looks into the mirrors. Mirrors of ... different social groups, different life roles, different hobbies, professions, stages of grief, durations of happiness. You look different in each one of them. They are all you, parts of you, and yet none of them are You. Humans are golems, amalgams. My identity sometimes feels hopelessly plastic because the things I once considered to be permanent no longer are ... I've graduated from schools, I've left my jobs, I've been disabled but now am healing, I had a loving nuclear family and now I do not. When all of this first began to change I thought this plasticity would be the end of Me. I had no clue who I was or what I should do. But as the years pass (as I read more books, watch more films, immerse in more art and world politics) I'm learning that it actually might actually be the only thing that's gotten me through. Perhaps instead of Plasticity, I should it call it Resilience. 🌾 . . . #pensivemood #pensivepost #drearydaythoughts #disabledandcute #chronicillness #chronicpain #spoonie #spoonielife #spoonieproblems #ehl#ehlersdanlosrome #ehlersdanlos #surgicalrecovery #butyoudontlooksick #girlswithdreads #girlswithpiercings #septumpiercing #fancyseptum #bigglasses
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Going to Dublin next week to spend my fiancé’s birthday with him. We’re Then going down to Kerry to the house down there and I am so excited. So two weeks worth of medication so I don’t run out. This me double the time and then I messed up double the times. 🤣 They make such a lovely noise when you shake them. . . . #sundaypillday #meds #medication #pillbox #chronicillness #chronicillnesses #dysautonomia #dysautonomiaawareness #pots #potssyndrome #posturalorthostatictachycardiasyndrome #potsie #eds #edstype3 #ehl#ehlersdanlossyndrome #ehlersdanlos #butyoudontlooksick #spoonie #spoonielife
38 2
My many years as a gymnast built me into who I am today in so many ways. I was fortunate to have only wonderful experiences with the sport, but as we’re learning more and more every day by the incredible, brave, strong women speaking out, so many girls and young women were not so fortunate. My heart breaks for the girls whose lives were ruined by Larry Nassar and the adults who enabled him to abuse and terrorize young gymnasts chasing their dreams for so many years. I have a lot of thoughts detailed in my latest blog post, link in bio. . . . #gym#gymnast/a> #gymnast #ehl#ehlersdanlosrome #eds #hypermobility #hypermobileeds #ehlersdanlos #flying #aerialist #alyraisman #mckaylamaroney #jordynweiber #simonebiles #jamiedantzscher #strongwomen #invisibleillness #butyoudontlooksick #healthybody #healthymind #womensupportingwomen #onceagymnastalwaysagymnast
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Weekends are for rest 💫💫 ——- Felt a ton better yesterday only to wake up with a slight cold 😂 (that’s what happens when they give you a steroid shot which shoots down your immunity) hoping you all have a lovely weekend ✨ . . . . . . . . . . . . . . #thegirlwhocanteat #model #modeling #gastroparesis #gp #tubie #eds #ehlersdanlos #ibd #crohnsdisease #greenbeauty #nontoxicbeauty #nontoxicmakeup #differentlyabled #chronicillness
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FREE LIVE TALK AT at 4 pm EST (1pm PT) in my Autoimmune Mastermind (link in profile to join 👆🏼): . . Christina and Courtney Maiorino will be speaking LIVE on How Having a Loving Relationship with our Diseases Has a Positive Impact on Our Lives. . . . Courtney and Christina, founders of @thethriveeffect, believe that health isn't one-dimensional - especially for those living with illness. . . They are proponents of cultivating harmony in all aspects of our lives to engender true health. They advocate that it's not just about what we eat and how often we move our bodies---mental, spiritual and emotional health are also key aspects of optimal well-being. . . Finding a balance between these many aspects of health can help us thrive with illness. . . Courtney @cmmaiori is a Certified Holistic Health Coach, Reiki Master, and Crohn's Disease thriver. . . Christina @clmaiorino is a classmate of mine earning her Master of Science degree in Human Nutrition and Functional Medicine and has overcome her own health challenges using holistic approaches. . . Tune in LIVE to interact and get all your burning questions answered! Just use the link in my profile or request to join the private Facebook group Empowered Autoimmune (*must answer entry questions to have your membership approved*). . . . . . . . . #autoimmunepaleo #aip #dysautonomia #myalgicencephalomyelitis #me #glutenfree #adrenalfatigue #lupus #autonomicdysfunction #has#hashimotos #celiac #anxiety #cfs #ibd #chronicfatigue #crohns #hyperadrenergicpots #hashimotos #paleo #yoga #holistic #momlife #hypothyroid #eds #pots #ehlersdanlos #fibromyalgia #empoweredautoimmune
59 6
Bon voilà petite nouvelle je dois allez à Thionville auprès du Dr Schroeder pour ma jambe #doublefracture #ligamentoplastie #ehl#ehlersdanlos et pour mon dos sa sera à la Pitié Salpêtrière à Paris auprès du Dr Antonio De Carvalho #ehlersdanlos #scoliotiquethoracolombaire lundi je dois appeler Paris et prendre rdv avec la clinique Notre Dame à Thionville voilà voilà quelques nouvelles
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Extricate yourself from the comparison game—the thief of joy and the ultimate root of many of our woes. The highlight reels others display on social media engenders the perception of perfection, but most of us fail to share our innermost fears, our long-repressed traumas, our feelings of inadequacy and unworthiness and ineptitude. A meticulously curated Instagram feed is not emblematic of who we truly are. It cannot possibly epitomize the essence of our character and the magnitude of our collective human suffering. As Lisa Nichols says, stop comparing your chapter four to someone else’s chapter twenty-four. Find peace with yourself irrespective of your progress, make space for laughter in the midst of sorrow, and cultivate joy in the face of despair. You are uniquely you, and your journey is quintessentially yours to define. . . Xo, Ali . . . . . . . . . . . #autoimmunepaleo #aip #dysautonomia #myalgicencephalomyelitis #me #glutenfree #adrenalfatigue #lupus #autonomicdysfunction #has#hashimotos #celiac #anxiety #cfs #ibd #chronicfatigue #crohns #hyperadrenergicpots #hashimotos #paleo #yoga #holistic #momlife #hypothyroid #eds #pots #ehlersdanlos #fibromyalgia #empoweredautoimmune
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@sarageurts, 26, has Ehlers-Danlos syndrome, a disorder that affects connective tissues and can cause some people to have elastic skin that stretches easily. “I believe your imperfections are individual to you and show the journey you have been on. I may have a disorder, and yes, my disorder is a part of me, but I am not my disorder,” she says. (photos by @brianaberglund)
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Today at 3 pm EST (12 noon PT), Sarah Morford, holistic nutritionist from @thecultivateblog will be speaking LIVE on Getting Real with POTS and Chronic Fatigue Syndrome (CFS): Holistic Healing Solutions in my Autoimmune Mastermind (link in bio 👆🏼)! . . Founder of Cultivate Holistic Living, Sarah works in a nutritional genomics practice and has conquered cancer, autoimmuune disease, chronic faigue syndrome (CFS), postural orthostatic tachycardia syndrome (POTS), and more using holistic approaches. . . Sarah is a big fan of “what ifs” and people living their dreams. She believes good health is a human right, and a healthy planet, a human responsibility. . . She created Cultivate with the mission to provide you with the seeds needed to grow a holistically healthy life, opening you up to a future spent harvesting your dreams, all while making our world a healthier place to live in the process. . . Don’t miss this opportunity to tune in and get your questions answered in real time. Sarah’s talk will be *audience-led* so she is counting on you for your questions! . . Please share this free resource with anyone suffering from CFS, myalgic encephalomyelitis (ME), dysautonomia, or Ehlers Danlos Syndrome (EDS) who could benefit. . . When you sign up, you’ll also hear 50 other free talks from 40+ other holistic health experts during this 30-day event (and if you miss the live, all the replays will be available through February 15!). . . After you enter your name and email, click the link to the private Facebook group in the confirmation email and *answer the required questions for entry into the group*. . . . . . . . . . #autoimmunepaleo #aip #dysautonomia #myalgicencephalomyelitis #me #glutenfree #adrenalfatigue #lupus #autonomicdysfunction #has#hashimotos #celiac #anxiety #cfs #ibd #chronicfatigue #crohns #hyperadrenergicpots #hashimotos #paleo #yoga #holistic #momlife #hypothyroid #eds #pots #ehlersdanlos #fibromyalgia #empoweredautoimmune
51 5
My Ehlers Danlos Syndrome Grrrrrls - this is one for you! 💜 Waiting for the Doctor surgery to open in the morning for my subluxed shoulder...it keeps rolling forward and I have a great deal of Scapula pain in the shoulder, but also shooting pain (feels like a nerve!) up my neck & into the back of my head. This is the 3rd big subluxation in three months...each month at the same time! You HAVE been telling me that menstruation & Hypermobililty are foes for some time. It would appear that the release of hormones around this time of my cycle is making my ligaments even LOOSER than they are...and this is happening. Oh and I only started menstruating three months ago after my body stopped for 12 months because I was so ill. What is your experience of PERIODS & HYPER MOBILITY? "That time of the month" lol #ehl#ehlersdanlosrome #ehlersdanlosgrrls #ehlersdanlos #EDS #period #periods #menstruation #timeofthemonth #hypermobility #hypermobile #sub#subluxn #sublux #autistic #actuallyautistic #autism #autisticvlogger #shoulderpain #neckpain #backpain #chronicillness #disability
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What an afternoon! Today I attended my first ever @ehlersdanlosuk group support meeting. In fact, it was the first time I met so many people with EDS in the same room. It was a thoroughly fascinating meeting, I learned a lot and hopefully shared some stuff that can help others - can’t wait to see how my new role with EDSUK pans out over the year! Now? Climbing time 😎 @ehlers.danlos #potssyndrome #ehl#ehlersdanlosrome #zebrastrong #ehlersdanlos #ehlersdanlossyndromeawareness #dysautonomia #dysautonomiaawareness #chronicillness #chronicpain #chronichealth #chronicfatigue #hypermobility #fodmap #sundaymotivation #sundaysupport #peersupport #thereishope #keepsmiling #keeptrying #keepongoing #isolation #buildingbridges #amputee #cancersurvivor #fitmuslimah #hijabspiration #climbergirl #paraclimbing #feelinghopeful
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15 0
Check out my new ride everyone! TiLite AeroX with Smartdrive MX2+. Here is an important PSA: NOT EVERYONE IN A WHEELCHAIR IS PARALYZED! Some of us have the use or limited use of our legs and that doesn't make us liars for using a wheelchair. Trust me, this is an expensive piece of equipment that was custom made to my body only after a doctor, two OTs, and my insurance decided I neeeded one. It's not something I can just pick up at Walgreens. In the end, don't make assumptions about people try asking them or you know just not making comments to strangers in Target. #ehlersdanlos #eds #zebrawarrior #tilite #wheelchair
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#Repost @bettergraces ・・・ Woken by my cats tumbling, rolling, fighting – I wonder what it's like to move freely, without considering such things as pain. Their small confident bodies crashing a path through our house. Such havoc but always something I welcome, preventing the ossification of a household with a sick person at its heart. I don't want that. Even though my body imposes a great deal that is burdensome, routine and unending – I still remember what it's like to have a house balanced differently, my younger brother living here too. I remember what it's like to live alone with PAs and carers coming in to help me. How that was at one and the same time terrifying – because I increasingly needed 24-hour care and couldn't fund it – and liberating. I am one woman who is not embracing a Grey Gardens life. It's just not what I want for myself. This sickness feels all-consuming; it often is. And yet I want the opposite of total seclusion: I want animals and outdoors and travel and people. The wheelchairs and medicines to make that happen? Whatever, that's fine. Just let me out of bed from time to time, world, whoever and whatever is listening. This is why I want to speak up for severely affected patients who can't even gain access to treatment, & at the same time advocate within my own field – poetry and the arts – for inclusion efforts which are stunningly absent for the most part. Only people living like this can tell you what it's like, what we need, how we're shut out. Please listen. #ehlersdanlos #ehlersdanlossyndrome #wheelchairlife #ableism #dysautonomia #creatives #poetsofig #poetryisnotdead #chronicpain #chronicillness #chronicfatigue #endometriosis #bronchiectasis #invisibleillness #peoplehopetribe #sickgirlproblems #mindbodysoul
70 0
Hey all, I haven't been doing well TLDR: I need a wheelchair, youcaring link in bio, please share . My chonic pain from EDS has been getting worse. Even my good knee has gone to shit. I can hardly walk during these flare-ups and when I do walk it causes me agonizing pain. I desperately need a wheelchair to help give me more mobility again. That's number one priority, but I need braces for my joints and forearm crutches or a rollater for the days when I can use my legs more easily (and of course doctors appointments and meds). My youcaring link is in my bio. If you could even just share it and get it out there, it would mean a lot #disabled#disability#disabledandcute#spoonie#spoonies#spoonielife#spooniestrong#eds#edszebra#heds#ehlersdanlossyndrome#ehlersdanlos#pots#potssyndrome#posturalorthostatictachycardiasyndrome#mobilityaid#wheelchair#wheelchairs#fundraiser#youcaring
17 2
wrists are good. wrists are helpful. somedays you just have to wrap the fucker up because you #sublux something and the bloody thing won't go back in properly. in other news, the single 'lemme see if i'm allergic/reactive to this type of material' roll of #cohesion #bandage passed it's first test run with flying colours, ie my wrist chilled out enough after a solid 14 hours and clicked all the way back on and stayed, and I've already #amazonprime some neon pink ones, to match the rest of my brace collection. #ehl#ehlersdanlosls #ehlersdanlossyndrome #ehlersdanlos #hypermobility #hypermobilityeds #dysautonomia #posturalorthostatictachycardiasyndrome #pots #potssyndrome #costochondritis #asthma #spoonie #chronicallyawesome #chronicallyill #wrists #subluxation #chronicillness #silverringsplint #ringsplint
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Another one of the many amazing ladies that you should be following already. Part 1/2 . @Regranned from @sarageurts - "And one day she discovered she was fierce, and strong, and full of fire, and that not even she could hold herself back because her passion burned brighter than her fears." - Mark A 📷 - @brianaberglund ❤ • • • • • • • • #weekend #saturday #morning #quote #photoshoot #photograpy #latepost #ocean #ehl#ehlersdanlosawareness #ehlersdanlos #effyourbeautystandards #inmyskiniwin #mybeautymyway #loveyourbody #loveyourlines #selflove #nowrongway #beyou #bebeautiful #blessed #inspire #embrace #beauty #happy #real #perfectlyimperfect #imperfections #model #WLYG #becomewilhelmina
21 0
En väldigt väldigt dålig dag är det för mig idag pga min EDS! 😰 #fuckeds #eds #ehl#ehlersdanlossyndrome #ehlersdanlos
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Do you feel like you know what your life's purpose is? Are you living a life in accordance with that?⠀ ⠀ If you'd like to, we'd love to hear what your "purpose" is... so many of us lack clarity around our purpose and what gives us meaning in our lives, that it might help others if you share.⠀ ⠀ ⠀ ⠀ ⠀ 🖤🖤🖤⠀ ⠀ #truthbomb #positivequotes #positivityforhypermobility #livingapositivehypermobilelife #hypermobility #hypermobilityspectrumdisorders #hypermobileEDS #positivehelpforhypermobility #theehlersdanlossyndromes #ehlersdanlos #edsawareness #loe#loeysdietzsyndrome #loeysdietz #loeysdietzaustralia #marfansyndrome #hypermobilityconnect #spoonie #zebra #chronicillness #pots #potsie #dysautonomia #chronicpain #chronicfatigue #mybendybody #hopeforhypermobility
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New video featuring this lovely human! ⭐️ We chat about our favourite youtubers, charities and things that make us feel better if we're down or anxious 💕 Go watch it (link in bio) and after go subscribe to @jerryalthea_ so you get notified when her video goes up later today. We get down and honest about chronic illnesses ❤️
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And there you have it. Per usual, mommy begins us to go to bed and we’ve been sleeping on and off for a few hours, and fast asleep for at least 20 minuets now! Meanwhile mommy can not for the life of her remember if she took her nighttime meds and isn’t tired yet because of that. Any good, cute, EDS/easy open pill holder reconditions out there? Mommy only takes them morning and night so that’s important! No in between stuff necessary! Thanks guys! WoofMew!! . . . . . #loveknowsnospecies #servicepup #sdit #rescuecat #fursisters #eds #ehlersdanlos #heds #medproblems #brainfog #pots #potssyndrome #posturalorthostatictachycardiasyndrome #fibromyalgia #fibrochick #chronicallyfabulous #chronicallyfighting #chronicallytired #chronicfatiguesyndrome #chronicpain #chronicinspiration #chronicpainproblems #invisibleillness #dislocations #subluxation #zebrastrong #zebrafamily #spoonie #spoonieprobs #woofmew
28 0
It's taken me a long time recognize the fact that I've battled eating disorders for years. Starting in the eleventh grade (2010-11) I dealt with emotional turmoil by starving myself. I went from 160 lbs to 114 in a matter of four months my junior year of high school. Over the years, my weight climbed again. In 2016 I went through a rough break-up and once again stopped eating. The first four photos are from the last two years of high school. The next three are from 2016. The last one is me today. Now, I'm actually obese. Since becoming ill and immobile, I gained a significant amount of weight. I'm now the heaviest I've ever been. Having a history of unhealthy eating and dieting has definitely caught up with me, and I'm now trying to navigate HEALTHY weight loss. I don't want to go back to my anorexic ways, but I know I am not at all happy with my body now. I struggle with binging, and need to get my eating under control, since EDS makes it extremely difficult and dangerous for myself to do any heavy sort of exercise. Moral of the story: you can have an eating disorder at any weight. It's always a struggle, and it's a mental illness. Since accepting the fact that I've suffered both anorexia and binge eating, I look back at photos of myself and wish that I could find myself in a happy middle ground. I'm determined to get there. 👍🏻
47 3
Didn’t have much pain today thankfully! Went to my boyfriends annual firefighter banquet and was able to celebrate with some great people😊🚒 #ehl#ehlersdanlosrome #ehlersdanlos #zebra #eds #spoonie #spoonielife #firefigher #firefightergirlfriend #boyfriend
22 1
Today's carrot harvest! Trying very hard to eat a bit better. Feels so good to cook with food I grew. Last year my husband built me tall raised garden beds, so I can garden in my wheelchair. Amazing to get back one of my favorite activities. Can't wait until it's time to plant in the spring! Until then, it's pretty cool to still be harvesting this late in the season. . . . . . . . . #eds #ehlersdanlos #ehlersdanlossyndrome #edslife #hypermobileeds #edsawareness #hypermobility #edswarrior #zeb#zebrastrong #wheelchair #wheelchairlife #disability #disabled #pain #chronicallyill #chronicillness #invisibleillness #dysautonomia #pots #chronicpain #chronicallyfabulous #edssucks #flare #zebra #zebrawarrior #spo#spoonielife #spoonie #harvest #gardening #raredisease
49 3
One of those discouraging but learning weeks in the gym. Discouraging because I did something to my back, shoulder, neck area. It is teaching me though that I will never be a heavy power lifter. Heavy weights and Ehlers Danlos do not mix. I don’t think any amount of muscle I gain will stop joint separation from happening with heavy weights but 🤷🏼‍♀️ a girl could dream....and get hurt to remind her. Going to develop a lower weight high rep workout plan for myself. Muscle can be gained through less intense lifting as well! Can’t stop won’t stop 💪🏼 . . #fitmom #fitmoms #igfitness #igfitmoms #momswholift #girlswholift #fitness #fitnessmotivation #fitnessinspiration #fitinspo #ehlersdanlos #ehlersdanlossyndrome #ehlersdanlosnationalfoundation #adaptivefitness #adaptedworkout
108 11
I promise i was trying to focus but my father kept calling me and ruining my score lol . . . . . #forestapp #studygram #studyblr #ehl#ehlersdanlosrome #ehlersdanlos #bujo #bulletjournaling #journaling #eds
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A weird day, I woke up in bucket loads of pain but by 1pm I was feeling better. Mornings can be like that sometimes. I taught Nicole how to play video games and that was very fun (and kind of hilarious sorry sis love you). Then I had a lovely little evening with the boyfriend. I did accidently fall and bite my lip rather badly, but it's all good just a tad swollen. Also really enjoying the warmer weather we've been having the past couple days. . . . Image description: Abby in her thin rimmed glasses smiling with her mouth open and looking up. She's in a green tee shirt . . .#eds #ehlersdanlos #ehlersdanlossyndrome #chronicillness #chronicallyill #spoonie #rsd #crps #complexregionalpainsyndrome #reflexsympatheticdystrophy #POTS #POTsie #posturalorthostatictachycardia #tachycardia #pain #disabled #disability #edstype3 #dysautonomia #edsawareness #EDSZebra #migraines #chronicfatigue #chronicpain #100InvisibleDays #wheelchairuser
132 2
Remi was such a good boy during our training session at the local library this morning! We also got to see some old friends and he did great around the small kiddos :) 🐩 🦓 #servicedog #assistancedog #mobilitydog #workingdog #medicalalert #ehlersdanlos #psychiatricservicedog #dysautonomia #servicedogsofinstagram #dog#dog#dog> #spoo #spoodlesofig #tasktrained #servicespoo #dogsofinsta #ehl#ehlersdanlossyndrome #madeintexasassistancedog #spoonie #invisibleillness #POTS #chronicillness #ehlersdanlossyndrome #dogs #mustloveremi #servicedogteam #poodle #standardpoodle #dog
43 0
THANK YOU to those of you who recommended @katefarms (@onehappymastie and others ☺️). I have been using Elecare, as I know it’s broken down in a way to prevent reactions, but Kate Farms tastes better and has better ingredients. There are actually some ingredients in it I would normally react to, so I was nervous, but I did very well with it!! On Tuesday, I’m meeting with my pediatrician to see if we could potentially get an epi and maybe think about seeing a different allergist for what my current allergist is calling “other mast cell neoplasm.” I will be going back to see my current allergist to see if he can provide any more help to me, but I want to be prepared in the likely chance he cannot. #ehlersdanlos #ehlersdanlossyndrome #eds #edszebra #zebrastrong #zebrawarrior #edsstrong #edswarrior #pots #posturalorthostatictachycardiasyndrome #potsstrong #potswarrior #allergies #allergicreactions #allergyissues #allergyprobs #mastcell #elecare #mcas ??
40 4
Trying to rest and start feeling better so wanted to post a photo of my favorite cleansing routine (second cleanse as I use my @nat@naturaholicshop Facial oil cleanser) here is my @lessisbeauty beautiful soap and my @naturaholicshop konjac sponge both such lovely products! I seriously feeling like the sponge had been game changer and has allowed me to use less product because it lathers so perfectly. . . . . . . . . . . . . . . #non#nontoxic #nontoxicbeauty #ski#skincare #organicskincare #skincare #nontoxic #lov#love #favorites #cleanser #konjacsponge #love #like #beauty #indiebeauty #thegirlwhocanteat #eds #ehlersdanlos #ibd #gastroparesis #crohnsdisease #tubie #lessisbeauty #ayuna #naturholic
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