top of page

4 things I Wish People Knew about Chronic Illnesses

Updated: Aug 16, 2024

Carole Abalekpor

August 14, 2024

 

  •  Just because you do not see it does not mean it is not real.

 

The concept of Invisible illnesses still seems to baffle some people. Something like MS may or may not have physical symptoms, but the disease overall affects your spine and brain by damaging the Myelin of the nerves, in turn disrupting the communication between your brain and other parts of your body. Though you cannot actively see this process happening, this can obviously affect someone in a very real way.

 

  •  There is no “Miracle Cure.”

 

There are plenty of things that can be cured with alternative medicine, i.e., honey to help with symptoms of a cold, or vapor rub for a stuffy nose. Unfortunately, chronic illness is often a lifelong struggle and thought there are different treatment options to help lessen symptoms, providing suggestion on how you cured your minor sickness does not necessarily help, and may even make someone with Chronic illness feel worse.

 

  •   I am not lazy; I am just struggling to function.

 

People with Chronic illness often feel as if they need to hide their symptoms because of the judgement from other people, sometimes diminishing your pain by saying “it’s not that bad” or insinuating that we are using it as an excuse, on the other hand, there is also the stigma of being viewed as weaker and “less than”. Someone suffering from a chronic illness may look ok on the outside, but they could be struggling to function throughout the day. It takes a lot of effort to manage chronic illness!

 

  •  It is ok to be Sad, It Sucks

 

For a lot of people, a diagnosis like this can be shocking, I mean after all, you just thought the doctor would have a simple explanation for all the symptoms you were having. It is ok to be sad, even angry about this! There is no time limit to grieving the person you were before this life changing event.

 


See more at Normalizeit.com

2 Comments


Elly
Nov 13, 2024

Having an invisible chronic illness sucks a lot. Especially having to fully know how to advocate for yourself at doctors appointments, but I feel it's really bad when random people tell you that you "Don't look like you have (x)". Not everyone can be so understanding, so it's nice when people want to know more about your illness to really know what you've been going through

Like
Guest
Nov 14, 2024
Replying to

Hello Elly!

I hope you are enjoying my content so far! Thank you for engaging..

I have had MS since I was 16 and have experienced this too many times to count and it is frankly alarming that this train of thought still exists.

Thank you so much for your engagement on my posts! I hope I am able to provide you support and validation with my blog!


if you are enjoying my content you can subscribe for free on the last page of my blog! 😀

Edited
Like
bottom of page