KitNipBox donates a portion of its proceeds to a variety of animal welfare organizations each month.
This blog is dedicated to blogging about nail polishes, nail polish designs, photography, cross stitch, etc. anything I do that is creative :)
Sunday, May 15, 2016
May KitNipBox
KitNipBox donates a portion of its proceeds to a variety of animal welfare organizations each month.
Saturday, May 14, 2016
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Thursday, May 12, 2016
Fibromyalgia Awareness Day
01. Sometimes the bath water cannot be hot enough
02. I cannot do it all
03. Naps are better sideways on my select comfort bed
04. Sleep pants should be acceptable in all facets of life and able to be worn year round :)
05. Good audio books can be your best friend driving to and from pt and dr's appointments
06. No matter what you do you can have a flare
07. People with fibro make the best listeners
08. I know what it feels like to not have energy to eat{or shower, or go to the bathroom}
09. It does not go away
10. even my cats can hurt me just by walking on me or putting a paw on me
11. Showers can hurt
12. Deep sleep is NECESSARY yet rare
13. There are a 100,000 treatments but no cure
14. People do not understand
15. Either do I
16. Money is not THAT important
17. I have had this longer than I thought
18. It takes forever to be diagnosed
19. Winter is EVIL
20. Change of seasons can be extremely painful
21. Changes of temperature can cause problems too
22. Not all symptoms make sense
23. Writing about it can be helpful
24. Having people tell me what I SHOULD do when I don't ask, is NOT acceptable
25. Errands/chores need to be done in clumps of time
26. Life takes more energy than it should
27. Society does not accept illness when you cannot see it
28. My priorities have changed {and they keep changing}
29. I thought getting diagnosed was THE battle
30. My husband loves unconditionally and is wonderful at living in the moment
31. Negativity drains my energy
32. "Spoon" theory
33. I require organization
34. Time in bed goes by faster than when awake
35. Covers are necessary
36. Fans are a necessity in the bedroom and in my office
37. I do the BEST I can
38. I am a Highly Sensitive Person
39. I wish people could be more understanding
40. I need lots of quiet and calm
41. For a long time I pretended to be Healthy
42. I struggle with feeling useless
43. I have to always remind myself I am not
44. I want to share my experience with others so they feel they have understanding and support
45. Fibromyalgia is only part of who I am and what I have to offer
46. I feel frustrated when I can't do more
47. people love to make fun of fibro patients
48. I love to cross stitch, walk, & work on my yard, but now rarely have the energy to do it. *Sigh*
49. If i cancel my plans with you, don’t be mad, I already feel bad
50. When I’m in a flare, leave me alone in a dark room (but check in), it makes me feel good
51. Every evening is tough as that's when it hits me
52. Your friend with Fibro that has no pain doesn’t make me feel any better
53. “You should exercise” My work day is my exercise
54. Certain foods make me flare-up (ie) peppers of any kind, etc.
55. Yes, diet matters but in flare mode, all bets are off
56. When i’m tired, let me sleep
57. Because of Fibro, I get to spend more time with my husband
58. Bright lights, loud noise and too many smells over-load my senses and make me nauseous
59. I play hide and go seek with the elements, too cold, too rainy, too hot, too much sun
60. To you, car rides are joy rides. To me, they’re a painful roller coaster ride.
61. Going to the doctor makes me mad, it’s a reminder of my condition
62. I can get moody, you would be too if you were in pain all the time, be patient with me
63. I can tell your mood as soon you walk in the room because my Fibro/spidey-senses are tingling
64. There are no no-pain days but my low-pain days are my happy days
Feel free to copy and paste and edit for your own use.......