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Chronically Ridiculous

Life Experiences and Advice for Living with chronically Ridiculous illnesses

Category: POTS

Healthy People, The Spoon Theory Doesn’t Apply To You

April 20, 2017April 20, 2017 Emily CodayLeave a comment

Note: I use able-bodied and healthy interchangeably as well as chronically ill and disabled interchangeably, but there are differences. As humans, we all have limitations. We can only go so long without sleep, rest, food, and water. We can only bear so much psychological stress. To have these limitations is to be human. Just because…

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9 Ways To Support Your Family Member With a Chronic Illness

February 16, 2017April 5, 2017 Emily CodayLeave a comment

People with chronic illnesses need all the support they can get- especially from their family. Here are some tips for truly supporting them. 1. Don’t Just Support Strangers, Support Your Family Most of my family are generous caring people- especially towards strangers. I regularly see them support children they don’t know and throw fundraisers for…

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do more

5 Responses to “Other Disabled People Agree You Should Be Doing More”

February 9, 2017February 19, 2017 Emily CodayLeave a comment

I’ve had so many terrible things said to me because of my chronic illness. “It is your fault you feel like this.” “If you try hard enough/ do more you won’t still be sick.” “If you just prayed harder god wouldn’t still let you be sick.” Needless to say, chronic illness has made for a difficult…

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Specialist Snowball Effect: When Referrals Get Out of Control

January 26, 2017February 3, 2017 Emily CodayLeave a comment

It is pretty standard for a doctor to refer their patients to a specialist when they are stumped or their knowledge is limited. It is a great practice to get better more specialized help. However, when a patient has a chronic illness, especially if it is one that isn’t well known, this can be a…

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When Your Doctor Deserves To Be Dumped

January 19, 2017February 2, 2017 Emily CodayLeave a comment

Finding the right doctor is a daunting task- especially when you have POTS. I think it is important to change the way we view doctors when you have a condition that the average doctor knows so little about. Instead of going to a doctor and taking their way as law, it is best to find…

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8 Ways Alternative Medicine Hurts People With Chronic Illnesses

December 18, 2016January 2, 2017 Emily Coday15 Comments

So before you consider the next random treatment suggested to you- check it out first. Is there any good evidence that it helps people with your condition? Is it worth the money, the false hope, the risk, or the blame you will likely receive when it fails?

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The Problem With Telling Patients They Will Grow Out Of POTS

October 27, 2016January 9, 2017 Emily Coday3 Comments

I had at least 5 different doctors inform me I would grow out of POTS. As a result, I stopped living and just survived, always waiting.

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Playing Pokemon Go as Someone With a Physical Disability

July 19, 2016 Emily Coday3 Comments

Pokemon Go is a new game that came out this past week and has already become a sensation with 15 million downloads already. The game encourages players to get out, get up, and get moving. The more a player walks around, the more gear they get, Pokemon they catch, the faster they level up, and…

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More #StopPOTS Feel Free To Share

May 5, 2016 Emily CodayLeave a comment

Feel free to share! All facts are from Dysautonomia International.

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#StopPOTS & Feel Free To Share

April 19, 2016 Emily Coday3 Comments

 

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  • Sexism & Chronic Illness
  • Healthy People, The Spoon Theory Doesn’t Apply To You
  • 9 Ways To Support Your Family Member With a Chronic Illness
  • 5 Responses to “Other Disabled People Agree You Should Be Doing More”
  • Misconceptions About Diet & Chronic Illness

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