#potsawarenessday — Public Fediverse posts

ME Research UK:

Oct 25 is PoTS Awareness Day. Read more about the condition and its relationship to ME/CFS on our website:
https://www.meresearch.org.uk/potsandmecfs/

#pots #posturalorthostatictachycardiasyndrome #potsawareness #potsawarenessday #mecfs #pwme @pots

ME Research UK:

Oct 25 is PoTS Awareness Day. Read more about the condition and its relationship to ME/CFS on our website:
https://www.meresearch.org.uk/potsandmecfs/

#pots #posturalorthostatictachycardiasyndrome #potsawareness #potsawarenessday #mecfs #pwme @pots

ME Research UK:

Oct 25 is PoTS Awareness Day. Read more about the condition and its relationship to ME/CFS on our website:
https://www.meresearch.org.uk/potsandmecfs/

#pots #posturalorthostatictachycardiasyndrome #potsawareness #potsawarenessday #mecfs #pwme @pots

ME Research UK:

Oct 25 is PoTS Awareness Day. Read more about the condition and its relationship to ME/CFS on our website:
https://www.meresearch.org.uk/potsandmecfs/

#pots #posturalorthostatictachycardiasyndrome #potsawareness #potsawarenessday #mecfs #pwme @pots

ME Research UK:

Oct 25 is PoTS Awareness Day. Read more about the condition and its relationship to ME/CFS on our website:
https://www.meresearch.org.uk/potsandmecfs/

#pots #posturalorthostatictachycardiasyndrome #potsawareness #potsawarenessday #mecfs #pwme @pots

It’s POTS Awareness Day. I forgot because (ironically) I’m dealing with monster coat hanger pain… something common in POTS.

It’s a terrible headache that encompasses your neck and upper back - it basically forms the shape of a coat hanger!

It took me years to realize the coat hanger pain was from my POTS. Years of suffering through debilitating headaches and back pain that painkillers couldn’t touch.

I tried massage, heat, ice, stretches, laying in a dark room…
Nothing worked.

You know what DID work? IV saline. When I get IV fluids I can feel the pain start to melt away. Relief tends to start at the top of my head and slowly moves down to my shoulders and back - the pain is generally gone after 1-2L.

It’s incredible just how much your body can be impacted by POTS. I’ve been dealing with this condition for years and I’m still learning new things every day.

It’s also a common comorbid with Long Covid. If you’re new to POTS, think you might have POTS or just want to learn more - I wrote an intro guide linked below:

https://www.disabledginger.com/p/living-life-upside-down-an-intro

CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #DysautonomiaAwarenessMonth #POTSAwarenessDay

It’s POTS Awareness Day. I forgot because (ironically) I’m dealing with monster coat hanger pain… something common in POTS.

It’s a terrible headache that encompasses your neck and upper back - it basically forms the shape of a coat hanger!

It took me years to realize the coat hanger pain was from my POTS. Years of suffering through debilitating headaches and back pain that painkillers couldn’t touch.

I tried massage, heat, ice, stretches, laying in a dark room…
Nothing worked.

You know what DID work? IV saline. When I get IV fluids I can feel the pain start to melt away. Relief tends to start at the top of my head and slowly moves down to my shoulders and back - the pain is generally gone after 1-2L.

It’s incredible just how much your body can be impacted by POTS. I’ve been dealing with this condition for years and I’m still learning new things every day.

It’s also a common comorbid with Long Covid. If you’re new to POTS, think you might have POTS or just want to learn more - I wrote an intro guide linked below:

https://www.disabledginger.com/p/living-life-upside-down-an-intro

CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #DysautonomiaAwarenessMonth #POTSAwarenessDay

It’s POTS Awareness Day. I forgot because (ironically) I’m dealing with monster coat hanger pain… something common in POTS.

It’s a terrible headache that encompasses your neck and upper back - it basically forms the shape of a coat hanger!

It took me years to realize the coat hanger pain was from my POTS. Years of suffering through debilitating headaches and back pain that painkillers couldn’t touch.

I tried massage, heat, ice, stretches, laying in a dark room…
Nothing worked.

You know what DID work? IV saline. When I get IV fluids I can feel the pain start to melt away. Relief tends to start at the top of my head and slowly moves down to my shoulders and back - the pain is generally gone after 1-2L.

It’s incredible just how much your body can be impacted by POTS. I’ve been dealing with this condition for years and I’m still learning new things every day.

It’s also a common comorbid with Long Covid. If you’re new to POTS, think you might have POTS or just want to learn more - I wrote an intro guide linked below:

https://www.disabledginger.com/p/living-life-upside-down-an-intro

CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #DysautonomiaAwarenessMonth #POTSAwarenessDay

It’s POTS Awareness Day. I forgot because (ironically) I’m dealing with monster coat hanger pain… something common in POTS.

It’s a terrible headache that encompasses your neck and upper back - it basically forms the shape of a coat hanger!

It took me years to realize the coat hanger pain was from my POTS. Years of suffering through debilitating headaches and back pain that painkillers couldn’t touch.

I tried massage, heat, ice, stretches, laying in a dark room…
Nothing worked.

You know what DID work? IV saline. When I get IV fluids I can feel the pain start to melt away. Relief tends to start at the top of my head and slowly moves down to my shoulders and back - the pain is generally gone after 1-2L.

It’s incredible just how much your body can be impacted by POTS. I’ve been dealing with this condition for years and I’m still learning new things every day.

It’s also a common comorbid with Long Covid. If you’re new to POTS, think you might have POTS or just want to learn more - I wrote an intro guide linked below:

https://www.disabledginger.com/p/living-life-upside-down-an-intro

CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #DysautonomiaAwarenessMonth #POTSAwarenessDay

It’s POTS Awareness Day. I forgot because (ironically) I’m dealing with monster coat hanger pain… something common in POTS.

It’s a terrible headache that encompasses your neck and upper back - it basically forms the shape of a coat hanger!

It took me years to realize the coat hanger pain was from my POTS. Years of suffering through debilitating headaches and back pain that painkillers couldn’t touch.

I tried massage, heat, ice, stretches, laying in a dark room…
Nothing worked.

You know what DID work? IV saline. When I get IV fluids I can feel the pain start to melt away. Relief tends to start at the top of my head and slowly moves down to my shoulders and back - the pain is generally gone after 1-2L.

It’s incredible just how much your body can be impacted by POTS. I’ve been dealing with this condition for years and I’m still learning new things every day.

It’s also a common comorbid with Long Covid. If you’re new to POTS, think you might have POTS or just want to learn more - I wrote an intro guide linked below:

https://www.disabledginger.com/p/living-life-upside-down-an-intro

CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #DysautonomiaAwarenessMonth #POTSAwarenessDay

To celebrate #POTSawarenessDay I stood up for slightly too long and now I'm dying 🫠

To celebrate #POTSawarenessDay I stood up for slightly too long and now I'm dying 🫠

To celebrate #POTSawarenessDay I stood up for slightly too long and now I'm dying 🫠

To celebrate #POTSawarenessDay I stood up for slightly too long and now I'm dying 🫠

To celebrate #POTSawarenessDay I stood up for slightly too long and now I'm dying 🫠

Huh, apparently it's #POTSawarenessDay. Personally I would like to have a day or two unaware of the flipping bastard 😔

Huh, apparently it's #POTSawarenessDay. Personally I would like to have a day or two unaware of the flipping bastard 😔

Huh, apparently it's #POTSawarenessDay. Personally I would like to have a day or two unaware of the flipping bastard 😔

Huh, apparently it's #POTSawarenessDay. Personally I would like to have a day or two unaware of the flipping bastard 😔

Huh, apparently it's #POTSawarenessDay. Personally I would like to have a day or two unaware of the flipping bastard 😔

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials. #PoTSAwarenessDay @DysSupport

@ukpots

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials. #PoTSAwarenessDay @DysSupport

@ukpots

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials. #PoTSAwarenessDay @DysSupport

@ukpots

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials. #PoTSAwarenessDay @DysSupport

@ukpots

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials. #PoTSAwarenessDay @DysSupport

@ukpots

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials.
💜More details: https://potsuk.org/wp-content/uploads/2024/09/PoTS-Pledge-1.pdf
#PoTSAwarenessDay @DysSupport

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials.
💜More details: https://potsuk.org/wp-content/uploads/2024/09/PoTS-Pledge-1.pdf
#PoTSAwarenessDay @DysSupport

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials.
💜More details: https://potsuk.org/wp-content/uploads/2024/09/PoTS-Pledge-1.pdf
#PoTSAwarenessDay @DysSupport

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials.
💜More details: https://potsuk.org/wp-content/uploads/2024/09/PoTS-Pledge-1.pdf
#PoTSAwarenessDay @DysSupport

💜Make a pledge to raise awareness of #PoTS throughout October #DysautonomiaAwarenessMonth
1) Share or take action with @UKPoTs daily posts/ideas.
2) Pledge an activity you enjoy and explain on your socials.
💜More details: https://potsuk.org/wp-content/uploads/2024/09/PoTS-Pledge-1.pdf
#PoTSAwarenessDay @DysSupport