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The ups and downs

Mar 23, 2017 11:45 AM

Just don't know if I can or want to get use to the never ending and always changing conditions of fibromayalgia and Lupus. I started doing and extra day of PT to try and help move things along. And I over did it a bit. So I wake up this morning to go to PT and was unable to walk. The pain was blinding and I've been forcing myself to make small steps in hopes that this GS will pop back. It's just hard to comprehend this is my life.

Mar 24, 2017 11:39 PM

Hey 😊 take it easy . I am sorry you are going through this. ((Gentle hugs )))) and lots of preyers your way . Don't give up .

Stay strong . 😊😊

Mar 25, 2017 11:59 AM

Yes, rest a bit. Have you asked about heated pool physical therapy? PT didn't help me until they tried the pool stuff. My body got stronger.

Mar 26, 2017 6:44 AM

You've got this newfibrogirl.. I know it's hard and I know that being in pain every day grates on your nerves. You can do this. We can all do this. The alternative is unacceptable and there has to be something to make it a bit better. {{Hugs}}🤗💕 I'll let you know when I find it..👌🏼

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