How Has Continuous Moderate To Severe Pain Affected Your Quality Of Life?
It affects me more in the fall/ winter when the weather is awful. But, sometimes in the spring and summer too. It’s hard to plan things or do anything when u feel like crap. But, I try hard to not live inside even though I’ve got a chronic disease. I lean I’m on my faith and started listening to Christian music when I’m down. Have a blessed day!!
I just feel like i am just existing my sons keep me going i would probably stay in bed all day if i didn't have them
My life has become a small world existing of running local errands and doctor visits, online friends, phone calls to my family out of state, gardening, crafts, etc. Making plans are a thing of the past as my level of symptom misery is determined day by day. What would I give for a 2 week vacation from fibro so I could travel to see my family. Fibro is lonely and isolating to this one very social person who thrived on being with people.
Yes definatly i can’t go out alone due the the nature of my migraines or drive . I struggle to do any repetitive motion because i go in spasm . I have been of work a long time . I dont make plans anymore , my friends understand if i say yes its on the day decision 🙌🫶❤️
I don’t do much anymore. I no longer have the manual dexterity to sew and embroider, gardening is limited to pots and planters since I can’t kneel much, and hiking is just impossible because I can’t walk for any length of time. I regularly have migraines now, which end any activity outside of a darkened quiet room. I retired right before the pandemic, and I know that timing has contributed to my isolation, but even without the socialization, I don’t really have my hobbies anymore. I’m an introvert, so I think this situation is easier on me than it might be for others, but I do find the pain to be very limiting.
How Much Does Stress Play Havoc On Your Fibro? And What Are Your Go-to's For Helping To Avoid A Flare Up During Stressful Times?
Sign up for free!