30 Things About My Invisible Illness You May Not Know

[Guest guest]

I have posted this before but some of the new ones may have not read it.  I am

not the " I " in this but we can all adapt it to our own situations.

 

Each September, National Invisible Chronic Illness Awareness Week is observed to

help educate the public and raise awareness about invisible illnesses.  This

year, one of the blogging activities is a " meme, " entitled “30 Things About My

Invisible Illness You May Not Know.â€Â  Here's mine...

1. The illness I live with is:  Fibromyalgia and ME/CFS

2. I was diagnosed with it in the year:  1996

3. But I had symptoms since:  1989

4. The biggest adjustment I’ve had to make is:  accepting that there are

things I just can't do anymore.

5. Most people assume: that chronic fatigue syndrome just means you're tired.

6. The hardest part about mornings are:  everything!  I don't do mornings.

7. My favorite medical TV show is:  I don't currently watch any medical

shows.  I used to like Strong Medicine.

8. A gadget I couldn’t live without is:  my computer.

9. The hardest part about nights are:  not being able to call people because

they're sleeping.  I'm a night owl and usually work all night, then sleep all

morning.

10. Each day I take 34 pills & vitamins. (No comments, please)

11. Regarding alternative treatments I:  use acupuncture and myofascial release

therapy – and love them!

12. If I had to choose between an invisible illness or visible I would choose: 

visible

13. Regarding working and career:  I'm thankful for computers and the Internet

which allow me to work from home so I am able to continue to support myself. 

14. People would be surprised to know:  that wearing clothes is painful.

15. The hardest thing to accept about my new reality has been:  the physical

limitations it has caused.

16. Something I never thought I could do with my illness that I did was:  have

a career helping others who have similar illnesses.

17. The commercials about my illness:  have done so much to improve awareness

and understanding of fibromyalgia.

18. Something I really miss doing since I was diagnosed is:  having an active

social life.

19. It was really hard to have to give up:  ballet dancing.

20. A new hobby I have taken up since my diagnosis is:  scrapbooking

21. If I could have one day of feeling normal again I would:  take my

grandchildren out for a day of fun.

22. My illness has taught me:  to prioritize – to spend what little energy I

have doing the things that are most important to me.

23. Want to know a secret? One thing people say that gets under my skin is:  If

you'd just exercise more, you'd feel better.

24. But I love it when people:  understand that just because I can't go

somewhere or do something with them doesn't mean I don't care. 

25. My favorite motto, scripture, quote that gets me through tough times is: 

And we know that all things work together for good to those who love God, to

those who are the called according to His purpose. – Romans 8:28

26. When someone is diagnosed I’d like to tell them:  to take charge of their

healthcare – learn everything they can about their illness and advocate for

themselves.

 

27. Something that has surprised me about living with an illness is:  how

drastically it can change your life.

28. The nicest thing someone did for me when I wasn’t feeling well was: 

clean my house.

29. I’m involved with Invisible Illness Week because:  I want to do whatever

I can to help others who are suffering and to educate the public about the

impact invisible illness can have on a life. 

30. The fact that you read this list makes me feel:  like you care and want to

make a difference, too.

 

Just take what you need from this and make it your own.

Kay_TX, AIH/PBC