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  • Reposted from @benola_cpi SEVENTH YEAR ANNIVERSARY CELEBRATION: Wednesday, 26th February 2020 - To the Glory of God and with a deep sense of appreciation for the dedication and support of our Board Members, our 7th Anniversary Cocktail Evening designed to send off a unique group of individuals who have given so much of their time and resjources to see to the successful actualization of the Benola Vision for Cerebral Palsy and Disability Management in Africa was a huge success. Held at our trademark venue, Peninsula Hotel and Towers, Providence Way, Lekki One, Lagos, the event was compact, full of fun and light banter. Of note was the candid and most encouraging comments from the out-going Board Members. 
So as we boldly step into our 8th year with a soon to be reinvigorated team, we humbly ask that you kindly join us to thank God and man for that which we have been able to achieve so far and pray for more blessings even as we embark on the incredible journey that lies ahead. 🙏🏾👌🏾👍🏾💪🏾🙌🏾👋🏾🤗🌹💃🕺🎉🎊 #anniversary #celebration #advisory #board #embers #old #new #thankgod #praisehim #appreciation #cerebralpalsy #cerebralpalsyawareness #advocacy #advocates #differentlyabled #disabled #disabilityisamindthing #abilityindisability #limitations #disability #disabilityawareness #specialones #specialneeds #inclusion #relationships #communityhealth #awareness  #interact #network  #support
  • Reposted from @benola_cpi SEVENTH YEAR ANNIVERSARY CELEBRATION: Wednesday, 26th February 2020 - To the Glory of God and with a deep sense of appreciation for the dedication and support of our Board Members, our 7th Anniversary Cocktail Evening designed to send off a unique group of individuals who have given so much of their time and resjources to see to the successful actualization of the Benola Vision for Cerebral Palsy and Disability Management in Africa was a huge success. Held at our trademark venue, Peninsula Hotel and Towers, Providence Way, Lekki One, Lagos, the event was compact, full of fun and light banter. Of note was the candid and most encouraging comments from the out-going Board Members.
    So as we boldly step into our 8th year with a soon to be reinvigorated team, we humbly ask that you kindly join us to thank God and man for that which we have been able to achieve so far and pray for more blessings even as we embark on the incredible journey that lies ahead. 🙏🏾👌🏾👍🏾💪🏾🙌🏾👋🏾🤗🌹💃🕺🎉🎊 #anniversary #celebration #advisory #board #embers #old #new  #thankgod #praisehim #appreciation #cerebralpalsy #cerebralpalsyawareness #advocacy #advocates #differentlyabled #disabled #disabilityisamindthing #abilityindisability #limitations #disability #disabilityawareness #specialones #specialneeds #inclusion #relationships #communityhealth #awareness #interact #network #support

  •  4  0  13 minutes ago
  • 🌜⭐Love y'all!⭐🌛
  • 🌜⭐Love y'all!⭐🌛

  •  7  3  14 minutes ago
  • Good morning y’all stay hydrated💦
  • Good morning y’all stay hydrated💦

  •  1  1  15 minutes ago
  • 🌜⭐Kawaii punk OOTD ❤️⭐🌛
  • 🌜⭐Kawaii punk OOTD ❤️⭐🌛

  •  9  14  16 minutes ago
  • So I had some fun with this ngl. I was playing around and just threw together a Fem Lucio test. Never have I ever had the urge to cosplay this stinky man but here I am and I’m kinda living for it. (Draft post)
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Tags
#cosplay #cosplayer #cosplaygirl #plussize #plussizecosplay #plussizecosplayer #plussizegirls #plussizequeen #cute #nonbinary #bisexual #bipride #lgbt #disabled #disabledcosplayer #fibromyalgia #fibromyalgiawarrior #alternative #alternativegirl #punk #punkgirl #alternativefashion #makeup #makeupartist #mua #shorthair #punkwannabe #thearcana #thearcanagame #thearcanacosplay
  • So I had some fun with this ngl. I was playing around and just threw together a Fem Lucio test. Never have I ever had the urge to cosplay this stinky man but here I am and I’m kinda living for it. (Draft post)
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    Tags
    #cosplay #cosplayer #cosplaygirl #plussize #plussizecosplay #plussizecosplayer #plussizegirls #plussizequeen #cute #nonbinary #bisexual #bipride #lgbt #disabled #disabledcosplayer #fibromyalgia #fibromyalgiawarrior #alternative #alternativegirl #punk #punkgirl #alternativefashion #makeup #makeupartist #mua #shorthair #punkwannabe #thearcana #thearcanagame #thearcanacosplay

  •  9  0  18 minutes ago
  • NEW episode with the absolutely wonderful @crippingupsex ! Eva Sweeney is truly an inspiration. We talk all about her amazing work to sexually liberate those with disabilities, give disabled people applicable sex education, a forum to ask questions and be heard, workshops to empower and more. As a person with cerebral palsy, we talk about growing up and the absolute lack of information available and how all of her work started. She’s such a powerhouse who is truly changing the world for the better and I’m grateful we got to speak with her. Please take a listen, link in bio!! .
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#podcast #podcaster #podcasts #podcastlove #sexpositive #sexuallyfluid #love #dating #sex #podcastersunite #podcastersofinstagram #new #listen #thursday #tbt #thursyay #losangeles #yum #findingmyyum #yummy #disabled #disability #disabledsex
  • NEW episode with the absolutely wonderful @crippingupsex ! Eva Sweeney is truly an inspiration. We talk all about her amazing work to sexually liberate those with disabilities, give disabled people applicable sex education, a forum to ask questions and be heard, workshops to empower and more. As a person with cerebral palsy, we talk about growing up and the absolute lack of information available and how all of her work started. She’s such a powerhouse who is truly changing the world for the better and I’m grateful we got to speak with her. Please take a listen, link in bio!! .
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    #podcast #podcaster #podcasts #podcastlove #sexpositive #sexuallyfluid #love #dating #sex #podcastersunite #podcastersofinstagram #new #listen #thursday #tbt #thursyay #losangeles #yum #findingmyyum #yummy #disabled #disability #disabledsex

  •  3  0  23 minutes ago
  • NEW episode of @findingmyyumpodcast with the absolutely wonderful @crippingupsex ! Eva Sweeney is truly an inspiration. We talk all about her amazing work to sexually liberate those with disabilities, give disabled people applicable sex education, a forum to ask questions and be heard, workshops to empower and more. As a person with cerebral palsy, we talk about growing up and the absolute lack of information available and how all of her work started. She’s such a powerhouse who is truly changing the world for the better and I’m grateful we got to speak with her. Please take a listen, link in bio!! .
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#podcast #podcaster #podcasts #podcastlove #sexpositive #sexuallyfluid #love #dating #sex #podcastersunite #podcastersofinstagram #new #listen #thursday #tbt #thursyay #losangeles #yum #findingmyyum #yummy #disabled #disability #disabledsex
  • NEW episode of @findingmyyumpodcast with the absolutely wonderful @crippingupsex ! Eva Sweeney is truly an inspiration. We talk all about her amazing work to sexually liberate those with disabilities, give disabled people applicable sex education, a forum to ask questions and be heard, workshops to empower and more. As a person with cerebral palsy, we talk about growing up and the absolute lack of information available and how all of her work started. She’s such a powerhouse who is truly changing the world for the better and I’m grateful we got to speak with her. Please take a listen, link in bio!! .
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    #podcast #podcaster #podcasts #podcastlove #sexpositive #sexuallyfluid #love #dating #sex #podcastersunite #podcastersofinstagram #new #listen #thursday #tbt #thursyay #losangeles #yum #findingmyyum #yummy #disabled #disability #disabledsex

  •  17  0  25 minutes ago
  • Reposted from @benola_cpi SEVENTH YEAR ANNIVERSARY CELEBRATION: Wednesday, 26th February 2020 - To the Glory of God and with a deep sense of appreciation for the dedication and support of our Board Members, our 7th Anniversary Cocktail Evening designed to send off a unique group of individuals who have given so much of their time and resjources to see to the successful actualization of the Benola Vision for Cerebral Palsy and Disability Management in Africa was a huge success. Held at our trademark venue, Peninsula Hotel and Towers, Providence Way, Lekki One, Lagos, the event was compact, full of fun and light banter. Of note was the candid and most encouraging comments from the out-going Board Members. 
So as we boldly step into our 8th year with a soon to be reinvigorated team, we humbly ask that you kindly join us to thank God and man for that which we have been able to achieve so far and pray for more blessings even as we embark on the incredible journey that lies ahead. 🙏🏾👌🏾👍🏾💪🏾🙌🏾👋🏾🤗🌹💃🕺🎉🎊 #anniversary #celebration #advisory #board #embers #old #new #thankgod #praisehim #appreciation #cerebralpalsy #cerebralpalsyawareness #advocacy #advocates #differentlyabled #disabled #disabilityisamindthing #abilityindisability #limitations #disability #disabilityawareness #specialones #specialneeds #inclusion #relationships #communityhealth #awareness  #interact #network  #support
  • Reposted from @benola_cpi SEVENTH YEAR ANNIVERSARY CELEBRATION: Wednesday, 26th February 2020 - To the Glory of God and with a deep sense of appreciation for the dedication and support of our Board Members, our 7th Anniversary Cocktail Evening designed to send off a unique group of individuals who have given so much of their time and resjources to see to the successful actualization of the Benola Vision for Cerebral Palsy and Disability Management in Africa was a huge success. Held at our trademark venue, Peninsula Hotel and Towers, Providence Way, Lekki One, Lagos, the event was compact, full of fun and light banter. Of note was the candid and most encouraging comments from the out-going Board Members.
    So as we boldly step into our 8th year with a soon to be reinvigorated team, we humbly ask that you kindly join us to thank God and man for that which we have been able to achieve so far and pray for more blessings even as we embark on the incredible journey that lies ahead. 🙏🏾👌🏾👍🏾💪🏾🙌🏾👋🏾🤗🌹💃🕺🎉🎊 #anniversary #celebration #advisory #board #embers #old #new  #thankgod #praisehim #appreciation #cerebralpalsy #cerebralpalsyawareness #advocacy #advocates #differentlyabled #disabled #disabilityisamindthing #abilityindisability #limitations #disability #disabilityawareness #specialones #specialneeds #inclusion #relationships #communityhealth #awareness #interact #network #support

  •  6  0  26 minutes ago
  • "Angela Lemond, RDN, LD, a national spokesperson for the Academy of Nutrition and Dietetics, tells her wheelchair user clients that they should focus on whole foods with minimal consumption of added sugars. Consumers who use wheelchairs all the time want to pack each meal with various colorful plant foods such as fruits, veggies, beans, legumes, and whole grains, as well as lean protein with an emphasis on fatty fish, like salmon and tuna to boost immunity." - Tracy Williams

Click the link in our bio for the full article.

#PUSHLiving
#ElevateDisability
#DisabilityInclusion
#HealthyLifestyle 
#wheelchair
#WheelchairLife
#LifeGoesOn
#LifeGoesOnWheels
#You_Can
#StayStrong
#HealthyLiving
#WheelchairNutrition
#confidence 
#selflove 
#selfcare 
#disabled
#loveyourself 
#wheelchairlife
  • "Angela Lemond, RDN, LD, a national spokesperson for the Academy of Nutrition and Dietetics, tells her wheelchair user clients that they should focus on whole foods with minimal consumption of added sugars. Consumers who use wheelchairs all the time want to pack each meal with various colorful plant foods such as fruits, veggies, beans, legumes, and whole grains, as well as lean protein with an emphasis on fatty fish, like salmon and tuna to boost immunity." - Tracy Williams

    Click the link in our bio for the full article.

    #PUSHLiving
    #ElevateDisability
    #DisabilityInclusion
    #HealthyLifestyle
    #wheelchair
    #WheelchairLife
    #LifeGoesOn
    #LifeGoesOnWheels
    #You_Can
    #StayStrong
    #HealthyLiving
    #WheelchairNutrition
    #confidence
    #selflove
    #selfcare
    #disabled
    #loveyourself
    #wheelchairlife

  •  6  0  27 minutes ago
  • This is the current situation. Snow. Loooads of snow. Too much snow to make it to the clinic to visit my daughter for the first time since monday. This is bullshit, and I’m caught somewhere between anger and sadness. It feels like, there’s just no way to look forward to ANYTHING, because it’s just not happening. Every single time! Anyway: this trip was way to dangerous to continue. Safety first. At least the clinic offered us the opportunity to call her though. Right now another heavy migraine is knocking me out AGAIN. So what, I took my medication- No time to cry, no time to die...I miss her, but she’s a warrior just like me. #fuckcancer #fucksnow #fuckanorexianervosa #fuckeatingdisorders #fuckwinter #depression #sad #mood #loveiseverything #recovering #recoveryanorexia #sober #queenoffuckingeverything #anorexianervosarecovery #fibromyalgia #disabled #love #family #proudmom #snow #montabaur
  • This is the current situation. Snow. Loooads of snow. Too much snow to make it to the clinic to visit my daughter for the first time since monday. This is bullshit, and I’m caught somewhere between anger and sadness. It feels like, there’s just no way to look forward to ANYTHING, because it’s just not happening. Every single time! Anyway: this trip was way to dangerous to continue. Safety first. At least the clinic offered us the opportunity to call her though. Right now another heavy migraine is knocking me out AGAIN. So what, I took my medication- No time to cry, no time to die...I miss her, but she’s a warrior just like me. #fuckcancer #fucksnow #fuckanorexianervosa #fuckeatingdisorders #fuckwinter #depression #sad #mood #loveiseverything #recovering #recoveryanorexia #sober #queenoffuckingeverything #anorexianervosarecovery #fibromyalgia #disabled #love #family #proudmom #snow #montabaur

  •  4  0  27 minutes ago
  • 🌜⭐Hey Moon fam! Missing you guys a lot! I'm getting a little better, but taking my time and readjusting to my new life on a set of wheels! There's been a lot of ups and downs, but I'm progressing with my anxiety and made some real progress! The one thing this journey had taught me is that progress isn't massive milestones, some days it's simply just watching the wildlife from my window and being at peace with my surroundings and most importantly, myself.⭐🌛
  • 🌜⭐Hey Moon fam! Missing you guys a lot! I'm getting a little better, but taking my time and readjusting to my new life on a set of wheels! There's been a lot of ups and downs, but I'm progressing with my anxiety and made some real progress! The one thing this journey had taught me is that progress isn't massive milestones, some days it's simply just watching the wildlife from my window and being at peace with my surroundings and most importantly, myself.⭐🌛

  •  38  3  30 minutes ago
  • SEVENTH YEAR ANNIVERSARY CELEBRATION: Wednesday, 26th February 2020 - To the Glory of God and with a deep sense of appreciation for the dedication and support of our Board Members, our 7th Anniversary Cocktail Evening designed to send off a unique group of individuals who have given so much of their time and resjources to see to the successful actualization of the Benola Vision for Cerebral Palsy and Disability Management in Africa was a huge success. Held at our trademark venue, Peninsula Hotel and Towers, Providence Way, Lekki One, Lagos, the event was compact, full of fun and light banter. Of note was the candid and most encouraging comments from the out-going Board Members. 
So as we boldly step into our 8th year with a soon to be reinvigorated team, we humbly ask that you kindly join us to thank God and man for that which we have been able to achieve so far and pray for more blessings even as we embark on the incredible journey that lies ahead. 🙏🏾👌🏾👍🏾💪🏾🙌🏾👋🏾🤗🌹💃🕺🎉🎊 #anniversary #celebration #advisory #board #embers #old #new #thankgod #praisehim #appreciation #cerebralpalsy #cerebralpalsyawareness #advocacy #advocates #differentlyabled #disabled #disabilityisamindthing #abilityindisability #limitations #disability #disabilityawareness #specialones #specialneeds #inclusion #relationships #communityhealth #awareness  #interact #network  #support
  • SEVENTH YEAR ANNIVERSARY CELEBRATION: Wednesday, 26th February 2020 - To the Glory of God and with a deep sense of appreciation for the dedication and support of our Board Members, our 7th Anniversary Cocktail Evening designed to send off a unique group of individuals who have given so much of their time and resjources to see to the successful actualization of the Benola Vision for Cerebral Palsy and Disability Management in Africa was a huge success. Held at our trademark venue, Peninsula Hotel and Towers, Providence Way, Lekki One, Lagos, the event was compact, full of fun and light banter. Of note was the candid and most encouraging comments from the out-going Board Members.
    So as we boldly step into our 8th year with a soon to be reinvigorated team, we humbly ask that you kindly join us to thank God and man for that which we have been able to achieve so far and pray for more blessings even as we embark on the incredible journey that lies ahead. 🙏🏾👌🏾👍🏾💪🏾🙌🏾👋🏾🤗🌹💃🕺🎉🎊 #anniversary #celebration #advisory #board #embers #old #new  #thankgod #praisehim #appreciation #cerebralpalsy #cerebralpalsyawareness #advocacy #advocates #differentlyabled #disabled #disabilityisamindthing #abilityindisability #limitations #disability #disabilityawareness #specialones #specialneeds #inclusion #relationships #communityhealth #awareness #interact #network #support

  •  7  0  32 minutes ago
  • 365 days on and my wounds have turned to scars.

I've just come home from councillingand and and it's the first time I've left the house and drove on my own for two weeks. My sessions are always emotional, as I explained how the last few weeks had played out.

I was asked if I ever sit with the emotion of life now and allow myself to feel sorry for myself. I cried as I said no. I cried as I admitted life is a million miles away from where I thought it would be 365 days on. My health has worsened and my bodies ability to do and cope with what it once did... Is no longer there.

We discussed help at home, and if there are any tools that can take the weight off my body or aid me in picking things up off the floor. We discussed that whilst I will come out of this flare eventually, I have to be realistic about the future and how likely it is that things could become more difficult.

I came home and hugged my husband and cried and cried. Life isn't perfect, things don't go to plan and sometimes you have to sit with that emotion and what that really feels like to you... To learn to start accepting things and start asking for more help.

I am chronically ill, even with a year of healing ✌️ #oneyear #anniversary #throwback #transformation #therapy #therapist #counselling #Fibromyalgia #fibro #endometriosis #endo #1in10 #invisableillness #chronicillness #chronicallyill #chronicallyawesome #chronicallyfabulous #postop #excision #nocure #progress #life #change #help #growth #hypermobility #spoonie #spoonielife #disabledandcute #disabled
  • 365 days on and my wounds have turned to scars.

    I've just come home from councillingand and and it's the first time I've left the house and drove on my own for two weeks. My sessions are always emotional, as I explained how the last few weeks had played out.

    I was asked if I ever sit with the emotion of life now and allow myself to feel sorry for myself. I cried as I said no. I cried as I admitted life is a million miles away from where I thought it would be 365 days on. My health has worsened and my bodies ability to do and cope with what it once did... Is no longer there.

    We discussed help at home, and if there are any tools that can take the weight off my body or aid me in picking things up off the floor. We discussed that whilst I will come out of this flare eventually, I have to be realistic about the future and how likely it is that things could become more difficult.

    I came home and hugged my husband and cried and cried. Life isn't perfect, things don't go to plan and sometimes you have to sit with that emotion and what that really feels like to you... To learn to start accepting things and start asking for more help.

    I am chronically ill, even with a year of healing ✌️ #oneyear #anniversary #throwback #transformation #therapy #therapist #counselling #Fibromyalgia #fibro #endometriosis #endo #1in10 #invisableillness #chronicillness #chronicallyill #chronicallyawesome #chronicallyfabulous #postop #excision #nocure #progress #life #change #help #growth #hypermobility #spoonie #spoonielife #disabledandcute #disabled

  •  11  0  32 minutes ago
  • Basically since Saturday night I’ve been to hospital 3 times for trying to end my life. That I’ve even stopped eating and drinking. Yesterday I saw the crisis team at home and they discharged me back to my gp even though I overdosed. They basically are so shit that when you ask for help you don’t get it you basically get told you know the consequences and it’s your responsibility as you have mental capacity. How hard is it to actually get them to acknowledge that you don’t feel safe with yourself as you just wanna top yourself constantly. As my borderline personality disorder is in full swing along with other mental health issues. Like today I got another letter from the hospital about testing for another condition so my physical and mental health isn’t great atm. They don’t seem interested whatsoever that even the police rang me Sunday morning etc! #gallbladdersurgery#gallstones#gallbladderremoval#operation#nervous#firstop#chronicillness#disabled#invisibleillness#pain#fibromyalgia#me#spoonie#mentalhealth#mental#health#complexptsd#depression#anxiety#borderlinepersonality#bulimia#bulimic!
  • Basically since Saturday night I’ve been to hospital 3 times for trying to end my life. That I’ve even stopped eating and drinking. Yesterday I saw the crisis team at home and they discharged me back to my gp even though I overdosed. They basically are so shit that when you ask for help you don’t get it you basically get told you know the consequences and it’s your responsibility as you have mental capacity. How hard is it to actually get them to acknowledge that you don’t feel safe with yourself as you just wanna top yourself constantly. As my borderline personality disorder is in full swing along with other mental health issues. Like today I got another letter from the hospital about testing for another condition so my physical and mental health isn’t great atm. They don’t seem interested whatsoever that even the police rang me Sunday morning etc! #gallbladdersurgery #gallstones #gallbladderremoval #operation #nervous #firstop #chronicillness #disabled #invisibleillness #pain#fibromyalgia#me#spoonie#mentalhealth#mental#health#complexptsd#depression#anxiety#borderlinepersonality#bulimia#bulimic!

  •  3  0  40 minutes ago
  • Warrior Lover
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Being a parent to a special needs kiddo is a blessing. I can speak first hand and say they are some of the strongest humans on this earth. The things they have to endure, push through and fight for are often times things we can easily take for granted.
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I remember when Bronx was a baby and feeling sad he couldn’t sit up unassisted like the other kids in his preschool. But he worked hard and has passed so many milestones we weren’t sure we would hit. He’s a warrior. +
Raise your hand if you have a warrior in your life or tag someone who does!
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One thing I love about this community is what we can learn from each other and how others stories can help us in our journey. I found @christinaasmallwood and watched her share fin’s story and it forever changed my perspective on our life with CP. thank you to all the people out there who are sharing their stories. We just hope to inspire someone with ours.
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Shirt is from my friend @christinaasmallwood from @fifiandmo
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#nosuchthingasnormal #nosuchthing #nevergiveup #advocatelikeamother #inclusion #diversity #diversityandinclusion #disabilityadvocate #differentnotless #specialneedsinfluencer #specialneedsmom #wheelchairlife #kindnessmatters #lovewins #cpwarrior #medicallycomplex #warriorlover #disabled #wheelchairmom
  • Warrior Lover
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    Being a parent to a special needs kiddo is a blessing. I can speak first hand and say they are some of the strongest humans on this earth. The things they have to endure, push through and fight for are often times things we can easily take for granted.
    +
    I remember when Bronx was a baby and feeling sad he couldn’t sit up unassisted like the other kids in his preschool. But he worked hard and has passed so many milestones we weren’t sure we would hit. He’s a warrior. +
    Raise your hand if you have a warrior in your life or tag someone who does!
    +
    One thing I love about this community is what we can learn from each other and how others stories can help us in our journey. I found @christinaasmallwood and watched her share fin’s story and it forever changed my perspective on our life with CP. thank you to all the people out there who are sharing their stories. We just hope to inspire someone with ours.
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    Shirt is from my friend @christinaasmallwood from @fifiandmo
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    #nosuchthingasnormal #nosuchthing #nevergiveup #advocatelikeamother #inclusion #diversity #diversityandinclusion #disabilityadvocate #differentnotless #specialneedsinfluencer #specialneedsmom #wheelchairlife #kindnessmatters #lovewins #cpwarrior #medicallycomplex #warriorlover #disabled #wheelchairmom

  •  34  4  55 minutes ago
  • ▪️ Blue Badge Holder 🚹♿🚺▪️
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After being denied, I finally got my disability badge a while ago and it has helped me so much and made life easier for sure. I am not very strong on my legs and I am not able to stand for  long periods of time. So having the blue badge has helped because even if I am in wheelchair or on the sticks I know I can park close to where ever I need to be 💜
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But I have to say the one thing I didn't expect when I first got the badge are the looks you get when you park in a disabled bay,  takes a little getting used too I have to say. 
Just because you are not in a wheelchair all the time, people feel the need to shout "that is a disabled bay"
Yes, I know thank you! I have a badge! 
It is frustrating because as I have said before just because your can't see something, doesn't mean it isn't there. Millions and millions of people are dealing with these debilitating invisible/chronic illnesses more awareness is needed! Invisible not dismissable! 🙌✨
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Sending love and positive vibes to you all my fellow warriors! 💜💜💜
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For more follow @potsiepains ✨💜
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#invisibleillness #chronicillness #invisibleillnessawareness #disabled
#ChronicPain #chronicfatigue #disability 
#fibro #fibromyalgiaawareness 
#fibromyalgiasucks #ehlersdanlos 
#hEDS #ehlersdanlossyndrome 
#chronicfatiguesyndrome #fibrolife 
#spoonielife #potsyndrome #pots
#seizures #notalldisabilitiesarevisible 
#butyoudontlooksick #disabledparking 
#mentalhealth #anxiety #depression 
#selfcare #selflove #anxietyfighter
#cbd #spoonie
  • ▪️ Blue Badge Holder 🚹♿🚺▪️
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    After being denied, I finally got my disability badge a while ago and it has helped me so much and made life easier for sure. I am not very strong on my legs and I am not able to stand for long periods of time. So having the blue badge has helped because even if I am in wheelchair or on the sticks I know I can park close to where ever I need to be 💜
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    But I have to say the one thing I didn't expect when I first got the badge are the looks you get when you park in a disabled bay, takes a little getting used too I have to say.
    Just because you are not in a wheelchair all the time, people feel the need to shout "that is a disabled bay"
    Yes, I know thank you! I have a badge!
    It is frustrating because as I have said before just because your can't see something, doesn't mean it isn't there. Millions and millions of people are dealing with these debilitating invisible/chronic illnesses more awareness is needed! Invisible not dismissable! 🙌✨
    .
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    Sending love and positive vibes to you all my fellow warriors! 💜💜💜
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    For more follow @potsiepains ✨💜
    .
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    #invisibleillness #chronicillness #invisibleillnessawareness #disabled
    #ChronicPain #chronicfatigue #disability
    #fibro #fibromyalgiaawareness
    #fibromyalgiasucks #ehlersdanlos
    #hEDS #ehlersdanlossyndrome
    #chronicfatiguesyndrome #fibrolife
    #spoonielife #potsyndrome #pots
    #seizures #notalldisabilitiesarevisible
    #butyoudontlooksick #disabledparking
    #mentalhealth #anxiety #depression
    #selfcare #selflove #anxietyfighter
    #cbd #spoonie

  •  39  4  1 hour ago
  • Excuse me but whoever put my body together forgot to put efficiently working lungs in my chest and I'd like a refund and to see your manager. 
This is the first nebuliser treatment of the year so that's pretty good but I still dislike it. Today has been pretty shit. For some reason I've been having a pretty few touch-and-go moments with seizures. Both with auras and without them so I'm not sure what's happening there and its playing with my asthma in an unpleasant way and that in turn is putting me in a foul mood. *Strops in a corner* 😡

#wiccansofinstagram #wicca #wiccan #wiccanspells #wiccanaltar #wiccalife #witch #meditation #esbat #sabbat #greenwiccan
#greenwicca #witchy #witchesofinstagram #witchcraft #witchyvibes #witchythings #witchesofinstagram🔮🌙 #chronicillness #chronicpainawareness #chronicpain #chronicpainsucks #chronicpainlife #disabledandcute #disabled  #chronicillnessawareness  #chronicbackpain #invisibleillness #notalldisbilitiesarevisable #seizures
  • Excuse me but whoever put my body together forgot to put efficiently working lungs in my chest and I'd like a refund and to see your manager.
    This is the first nebuliser treatment of the year so that's pretty good but I still dislike it. Today has been pretty shit. For some reason I've been having a pretty few touch-and-go moments with seizures. Both with auras and without them so I'm not sure what's happening there and its playing with my asthma in an unpleasant way and that in turn is putting me in a foul mood. *Strops in a corner* 😡

    #wiccansofinstagram #wicca #wiccan #wiccanspells #wiccanaltar #wiccalife #witch #meditation #esbat #sabbat #greenwiccan
    #greenwicca #witchy #witchesofinstagram #witchcraft #witchyvibes #witchythings #witchesofinstagram🔮🌙 #chronicillness #chronicpainawareness #chronicpain #chronicpainsucks #chronicpainlife #disabledandcute #disabled  #chronicillnessawareness  #chronicbackpain #invisibleillness #notalldisbilitiesarevisable #seizures

  •  5  1  1 hour ago
  • Breathe. Just take it one day at a time 
#dailyselfies
  • Breathe. Just take it one day at a time
    #dailyselfies

  •  3  1  1 hour ago
  •  39  1  1 hour ago
  • “I don’t think of all the misery but of the beauty that still remains” ~Anne Frank
  • “I don’t think of all the misery but of the beauty that still remains” ~Anne Frank

  •  50  7  1 hour ago
  • Hi everybody! It’s Alex! I would love to get a few more followers if people will help me. I am a #cancer fighter, I’m #Disabled 🦿, I’m passionate about #nature & #wildlife and protecting our natural world 🌍 I love #Owls 🦉 and I love #Archery 🏹 . I’m part of the #Police Family! And I love #DoctorWho #DrWho 🇬🇧🇺🇸🇨🇦
  • Hi everybody! It’s Alex! I would love to get a few more followers if people will help me. I am a #cancer fighter, I’m #Disabled 🦿, I’m passionate about #nature & #wildlife and protecting our natural world 🌍 I love #Owls 🦉 and I love #Archery 🏹 . I’m part of the #Police Family! And I love #DoctorWho #DrWho 🇬🇧🇺🇸🇨🇦

  •  54  2  1 hour ago
  • Really, how are you? I’m going to go first and say that while I’ve been on the good side of things for several days now, I find my thoughts drifting through deep worry, despair and fear. I’m trying to keep up with the news about the coronavirus and it’s of course making me think of the worldwide community of folks who have health challenges. Not only that, but those who have mental health challenges that make situations like the potential of this one extremely frightening, tho it’s enough to make anyone afraid. I’m trying to stay grounded, but this morning I wondered what it might be like in someone else’s head so here I am with this post. Feel free to share here if you want and know I’m holding your hand through the interwebs. 💜 big hugs #chronicillness #spoonie #disabled #letstalk #coronavírus
  • Really, how are you? I’m going to go first and say that while I’ve been on the good side of things for several days now, I find my thoughts drifting through deep worry, despair and fear. I’m trying to keep up with the news about the coronavirus and it’s of course making me think of the worldwide community of folks who have health challenges. Not only that, but those who have mental health challenges that make situations like the potential of this one extremely frightening, tho it’s enough to make anyone afraid. I’m trying to stay grounded, but this morning I wondered what it might be like in someone else’s head so here I am with this post. Feel free to share here if you want and know I’m holding your hand through the interwebs. 💜 big hugs #chronicillness #spoonie #disabled #letstalk #coronavírus

  •  4  0  1 hour ago
  • One of the hardest things about having a disability, is that is what people see first.  One you meet up with people there is always the same question about my condition, have you tried this or that, and then you get the poor you.  People have good intentions, but I don’t want to be just CRPS or be as poor old me, I just want to be me.  Does that make sense?

#crps #type2crps #complexregionalpainsyndrome #chronicillness #chronicpain #chronicfatigue #painmanagement #disablednotdefeated #disabilityawareness #disabledlife #crpswarrior #crpsawareness #crpsstrong #chronicpainwarrior #chronicpainawareness #chronicpainlife #mentalhealth #health #wellness #mentalhealthawareness #mentalhealthisimportant #mentalhealthsupport #mindset #mindfulmovement #lifewithcrps #lifewithadisability #disabled
  • One of the hardest things about having a disability, is that is what people see first. One you meet up with people there is always the same question about my condition, have you tried this or that, and then you get the poor you. People have good intentions, but I don’t want to be just CRPS or be as poor old me, I just want to be me. Does that make sense?

    #crps #type2crps #complexregionalpainsyndrome #chronicillness #chronicpain #chronicfatigue #painmanagement #disablednotdefeated #disabilityawareness #disabledlife #crpswarrior #crpsawareness #crpsstrong #chronicpainwarrior #chronicpainawareness #chronicpainlife #mentalhealth #health #wellness #mentalhealthawareness #mentalhealthisimportant #mentalhealthsupport #mindset #mindfulmovement #lifewithcrps #lifewithadisability #disabled

  •  3  0  1 hour ago
  • Roo was born without front legs. His human, Steve, was injured in a horrible car crash that left him paralyzed from the waist down. They were destined to find eachother. ❤️ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀
Follow @localish for more good news to brighten your day, every day! ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀
#fosterdog #fosteringsaveslives #fosterdogsofinstagram #disableddogs #rescue #rescuedog #doglovers #dogloversofinstagram #specialneedsdogs #disabledandcute #disabled #cute #cutevideos #mademesmile #feelgood #feelgoodvideos #amazing #love #faith #fate #destiny #abc #abclocalish #localish
  • Roo was born without front legs. His human, Steve, was injured in a horrible car crash that left him paralyzed from the waist down. They were destined to find eachother. ❤️ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀
    Follow @localish for more good news to brighten your day, every day! ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀
    #fosterdog #fosteringsaveslives #fosterdogsofinstagram #disableddogs #rescue #rescuedog #doglovers #dogloversofinstagram #specialneedsdogs #disabledandcute #disabled #cute #cutevideos #mademesmile #feelgood #feelgoodvideos #amazing #love #faith #fate #destiny #abc #abclocalish #localish

  •  60  2  1 hour ago

Top #disabled Posts

  • So ein Mistwetter 🙋🏻‍♂️🙈 irgendwie habe ich das Gefühl, dass dieses Mistwetter nicht aufhört! Wir haben uns fürs Wochenende ein Hotel in Hamburg gemietet und wollen dort ein bisschen rum gucken und zu König der Löwen gehen! Ich hoffe, dass dieses Wetter bis dahin ein bisschen aufhört 😅🙋🏻‍♂️ Obwohl, zu Hamburg, passt dieses Wetter ja 😉 Hafen, Wasser dies das 😎. Ich war mit meiner Tochter heute bei Oma zu Besuch, lecker Kuchen essen und Tee trinken! Was habt ihr bei diesem Dreckswetter gemacht? ❤️ #schmuddelwedda #rain #regen #kalt #garten #handicap #disabled #krücken #crutches #marekroscher #ostfriesland #niedersachsen
  • So ein Mistwetter 🙋🏻‍♂️🙈 irgendwie habe ich das Gefühl, dass dieses Mistwetter nicht aufhört! Wir haben uns fürs Wochenende ein Hotel in Hamburg gemietet und wollen dort ein bisschen rum gucken und zu König der Löwen gehen! Ich hoffe, dass dieses Wetter bis dahin ein bisschen aufhört 😅🙋🏻‍♂️ Obwohl, zu Hamburg, passt dieses Wetter ja 😉 Hafen, Wasser dies das 😎. Ich war mit meiner Tochter heute bei Oma zu Besuch, lecker Kuchen essen und Tee trinken! Was habt ihr bei diesem Dreckswetter gemacht? ❤️ #schmuddelwedda #rain #regen #kalt #garten #handicap #disabled #krücken #crutches #marekroscher #ostfriesland #niedersachsen

  •  233  36  25 February, 2020
  • 𝐈𝐧𝐯𝐢𝐬𝐢𝐛𝐥𝐞 ≠ 𝐈𝐦𝐚𝐠𝐢𝐧𝐚𝐫𝐲

As sick as it may sound, I’ll admit, there have been times when I almost wish I were worse off— that my illnesses, and the pain that comes with each, were on display for all to witness. In fiction literature and comic books, invisibility is considered a superpower. 🦸🏼‍♀️ But, in my life and in the lives of many others, invisibility has done more harm than it has good. •

I don’t fit into society’s perception of what a disabled individual looks like. ♿️ And because of that, I constantly feel like I’m having to prove myself. I feel like I have to “prove” my illness— and, yes, it feels as screwed up as it sounds. 🤷🏼‍♀️ Society demands an explanation, and because of that, I’ve often found myself apologizing for my own existence— for taking up space, for needing accommodations... •

I am not entirely sure why those of us living with invisible disabilities feel we have to explain and justify ourselves to others. I’ve racked my brain wondering what I needed to do for others to “get it.” Should I share my endless medical records? Make sure my port-a-cath tubing is on display when I venture into public? Throw a party every time I get referred to another specialist? Or receive a new prescription? Vlog my 3-4x/weekly infusions? •

I hope that someday I can stop apologizing. I hope you can, too.
  • 𝐈𝐧𝐯𝐢𝐬𝐢𝐛𝐥𝐞 ≠ 𝐈𝐦𝐚𝐠𝐢𝐧𝐚𝐫𝐲

    As sick as it may sound, I’ll admit, there have been times when I almost wish I were worse off— that my illnesses, and the pain that comes with each, were on display for all to witness. In fiction literature and comic books, invisibility is considered a superpower. 🦸🏼‍♀️ But, in my life and in the lives of many others, invisibility has done more harm than it has good. •

    I don’t fit into society’s perception of what a disabled individual looks like. ♿️ And because of that, I constantly feel like I’m having to prove myself. I feel like I have to “prove” my illness— and, yes, it feels as screwed up as it sounds. 🤷🏼‍♀️ Society demands an explanation, and because of that, I’ve often found myself apologizing for my own existence— for taking up space, for needing accommodations... •

    I am not entirely sure why those of us living with invisible disabilities feel we have to explain and justify ourselves to others. I’ve racked my brain wondering what I needed to do for others to “get it.” Should I share my endless medical records? Make sure my port-a-cath tubing is on display when I venture into public? Throw a party every time I get referred to another specialist? Or receive a new prescription? Vlog my 3-4x/weekly infusions? •

    I hope that someday I can stop apologizing. I hope you can, too.

  •  585  31  21 hours ago
  • Non ho il coronavirus quindi non sono contagiosa!!!
Non lo è nemmeno la mia disabilità!!!
Oggi con questo costume ho voluto sdrammatizzare su un tema molto serio che sta affliggendo l’intera popolazione ed al contempo far capire che della disabilità non bisogna aver paura, perché è una condizione fisica. Anzi se più persone imparassero a conoscerla e dunque a rispettarla ne trarremmo tutti vantaggio e dunque vivremmo tutti meglio. 
W la vita!!!
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#coronavírus #coronavirüs #virus #virale #virales #contagioso #contagio #disabilità #disability #disabilities #disabled 
#carnevale #carnevale2020 #carnevalecostumi #carnevaledivenezia  #consigli  #robertamacrí #robertamacrístyle #leichenullapuómatuttofa #nullaèimpossibilebastavolerlo #nevergiveup #power #lifestyle #lifecoach #lifeonwheels #lifestyleblogger #lifemotivation #tbt #influencerstyle #influencerlife
  • Non ho il coronavirus quindi non sono contagiosa!!!
    Non lo è nemmeno la mia disabilità!!!
    Oggi con questo costume ho voluto sdrammatizzare su un tema molto serio che sta affliggendo l’intera popolazione ed al contempo far capire che della disabilità non bisogna aver paura, perché è una condizione fisica. Anzi se più persone imparassero a conoscerla e dunque a rispettarla ne trarremmo tutti vantaggio e dunque vivremmo tutti meglio.
    W la vita!!!
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    #coronavírus #coronavirüs #virus #virale #virales #contagioso #contagio #disabilità #disability #disabilities #disabled
    #carnevale #carnevale2020 #carnevalecostumi #carnevaledivenezia #consigli #robertamacrí #robertamacrístyle #leichenullapuómatuttofa #nullaèimpossibilebastavolerlo #nevergiveup #power #lifestyle #lifecoach #lifeonwheels #lifestyleblogger #lifemotivation #tbt #influencerstyle #influencerlife

  •  444  20  25 February, 2020
  • Mantra de hoje: “É PROIBIDO ESTACIONAR NA VIDA!”
Você pode tudo, menos desistir.
Algumas tempestades chegam apenas para testar a força das nossas raízes.
Vista-se de sorriso, tá na moda!😄❤️
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Cadeira Smart Vega @lojadocadeirante @smartcadeiraderodas ♿️
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Ph: @rm.drone 📸💕
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#disability #beauty #wheelchairs #diversity #inclusivity #tattoo #lifestyle #model #disabled #modelo #disabledfashion #saopaulointerior #lifeonwheels #americanasp #photography #photooftheday
#cadeirante #lesaomedular  #digitalinfluencer #wheelchairwoman #fashion #canonbr #omelhorclick #clickdoiniciante #ensaioexterno 
#photo #photoshoot #modeling
  • Mantra de hoje: “É PROIBIDO ESTACIONAR NA VIDA!”
    Você pode tudo, menos desistir.
    Algumas tempestades chegam apenas para testar a força das nossas raízes.
    Vista-se de sorriso, tá na moda!😄❤️
    .
    .
    .
    .
    .
    Cadeira Smart Vega @lojadocadeirante @smartcadeiraderodas ♿️
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    Ph: @rm.drone 📸💕
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    #disability #beauty #wheelchairs #diversity #inclusivity #tattoo #lifestyle #model #disabled #modelo #disabledfashion #saopaulointerior #lifeonwheels #americanasp #photography #photooftheday
    #cadeirante #lesaomedular  #digitalinfluencer #wheelchairwoman #fashion #canonbr #omelhorclick #clickdoiniciante #ensaioexterno
    #photo #photoshoot #modeling

  •  638  42  25 February, 2020
  • Always time for a selfie. Considering this was 4 years ago tomorrow I’m not surprised the last few days I’ve had a bit of a weird feeling like something was coming. It’s a feeling that’s happened every year since the start of my Lemtrada journey. This year I’m thankful I have to scroll back through thousands of photos to find a picture like this. Two rounds of Lemtrada and nothing since. I felt a load of emotions when Lem was pulled as a first line treatment. It’s crap that it comes with so many risks, I’ve seen first hand people develop some nasties from it but I’ve also seen people have amazing results. I’m not out of the woods yet but so far I can honestly say I have no regrets. I’m angry for all those people living with MS who have an option taken away I knew the risks and for me, honestly the stakes of what could happen if I didn’t pick my first treatment as a hard one were too high. I’m no medical expert but I see little value in starting on lower risk treatments that are  moderately effective. Maybe I will do a post another time about my thoughts on this. If you’ve read this far then well done here is something I’ve not really said before - how I was in June 2015 scares the shit out of me I get too comfortable with the fact I’ve not relapsed EVER! Sometimes I feel it important to remember how I was I don’t let it consume my life but I do make sure I am comfortable with the possibility that it’s happened once and it could happen again. It isn’t a bad or negative thing to think like that it’s realistic and it’s what helps me. It’s also okay to feel guilty I know I do because I feel lucky compared to others but equally there are more people out there without MS that are luckier than I am. So this weekend will be a mixture of reflection, celebration (might even get a cake!) and just feeling what ever emotions I need to feel! #ms #multiplesclerosis #thisisms #mslife #livingwithms #autoimmunedisease #invisibleillness #disabilityawareness #disability #disabled #alemtuzumab #lemtrada #addenbrookes #treatment #mser #relapse #relapsefree #cake #thoughtoftheday #thoughts
  • Always time for a selfie. Considering this was 4 years ago tomorrow I’m not surprised the last few days I’ve had a bit of a weird feeling like something was coming. It’s a feeling that’s happened every year since the start of my Lemtrada journey. This year I’m thankful I have to scroll back through thousands of photos to find a picture like this. Two rounds of Lemtrada and nothing since. I felt a load of emotions when Lem was pulled as a first line treatment. It’s crap that it comes with so many risks, I’ve seen first hand people develop some nasties from it but I’ve also seen people have amazing results. I’m not out of the woods yet but so far I can honestly say I have no regrets. I’m angry for all those people living with MS who have an option taken away I knew the risks and for me, honestly the stakes of what could happen if I didn’t pick my first treatment as a hard one were too high. I’m no medical expert but I see little value in starting on lower risk treatments that are moderately effective. Maybe I will do a post another time about my thoughts on this. If you’ve read this far then well done here is something I’ve not really said before - how I was in June 2015 scares the shit out of me I get too comfortable with the fact I’ve not relapsed EVER! Sometimes I feel it important to remember how I was I don’t let it consume my life but I do make sure I am comfortable with the possibility that it’s happened once and it could happen again. It isn’t a bad or negative thing to think like that it’s realistic and it’s what helps me. It’s also okay to feel guilty I know I do because I feel lucky compared to others but equally there are more people out there without MS that are luckier than I am. So this weekend will be a mixture of reflection, celebration (might even get a cake!) and just feeling what ever emotions I need to feel! #ms #multiplesclerosis #thisisms #mslife #livingwithms #autoimmunedisease #invisibleillness #disabilityawareness #disability #disabled #alemtuzumab #lemtrada #addenbrookes #treatment #mser #relapse #relapsefree #cake #thoughtoftheday #thoughts

  •  140  5  22 February, 2020