Chronic Pain Support Group
Physicians and professionalsdefine pain as chronic if it lasts longer than three to six months and is persistent. It's distinct from acute pain that is a direct result of injury or trauma. This support group is dedicated to those suffering from chronic pain. Discuss treatments that have worked for you, find advice for your specific experience, and find support. You're not...
I'm not proud of it, but if I'd had tried to move around, especially with a 2 year old, I would've been putting myself in a worse situation. I guess it's something most of us have to live with. But at least we HAVE that med to help- a lot of CP patients don't have anything,
Then trying to not let pain get too far out ahead of me on breakthrough meds........'cause they won't be as relieving if I wait too long........
Frankly...I miss a life without meds all together....
Though, I'd have no life at all without them..
Hugs....jc..
I went to a potluck and my employer of eight yrs that forced me out. I left in tears because I miss working so much. I think I isolate from friends cause I have to face reality when I see them.
I am so grateful for this group andtalking with others who understand that it sucks to wait for meds all time, that lying in bed is not as fun as it seems. or getting out of chores cause I dont feel good....id rather be productive. Cp causes guilt. My mind has a busy day and plans, but my body disagrees.
will this pain and loss make me bitter and mean in time?
I'm always saying just waiting for painkillers to kick in but half the time they don't.
It's hard living like this, al ways w aiting.
Al ways happen they, all day long.
I try really hard to not say that to my kids too often but, it is either that or "sorry honey, I can't right now"
HUGS my friends in pain.
I say that too, I think we all must, looks like from your thread.
the worst part is when I know that even If I take more, it is not going to help me so I am left with most of the day left and just knowing it's not gonna be fun.
Hugs to you and all who know this feeling.
Man, last week there were alot of tears because bt meds weren't working. Today I am grateful that about half of the time the bt meds work and that allows me some freedom.
you will get over it. CP is a thief, but it's also a giver of compassion and new friends and a new way of appreciating things you may never have noticed. not to be pollyanna.
this group is a wonderful lifeline to so many of us. we're here and all going through all the phases all the time.
i hope today has been a better day. hugs and love!
I am not currently taking any pain medicine. I would like to, I just don't know what I could take that would not hurt my ulcers from Crohn's disease. My best friend right now is my heating pad. It does not take the pain away, but it is soothing. I am not looking forward to the summer...
I am sorry so many people are in such pain. Feeling helpless to do something and not being able to take action in some way to make things better, really sucks. I try to see the funny and try not to get too depressed. It does creep in now and then...
Good luck everyone. :)
I find I usually have to suck it up and get started on something easy and take lots of breaks if I need to. Then at least I have gotten a start and tend to stick to whatever it is that needs to get done.
I also try to get something done most days so that things don't start to really pile up on me. It is really demotivating when, "EVERYTHING NEEDS TO BE DONE". So I spread my simple day to day chores out over the course of the week.