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Old 11-22-2016, 06:23 AM
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CRPSbe CRPSbe is offline
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Join Date: Mar 2009
Location: Belgium, Europe
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15 yr Member
CRPSbe CRPSbe is offline
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Join Date: Mar 2009
Location: Belgium, Europe
Posts: 832
15 yr Member
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Quote:
Originally Posted by Shay08 View Post
Sorry to hear that you are going through a bad flareup. Yes, weather, especially cold or windy weather, can cause flareups. Some people are sensitive to changes in the barometric pressure. You also mentioned that your arthritic knee is acting up. I have found that pain in other areas of the body can trigger a flareup in the CRPS affected limb(s). Add stress, fatigue, or some weird thing like vibration and things can get pretty bad.

It doesn't necessarily mean that the meds are no longer effective. Take away the weather issues, other pain, stress, etc. and those same meds may still be effective. Many people are prescribed a different medication for breakthrough pain. See if things improve on their own and discuss this with your doctor.

In the meantime, dress for the warmth that you personally need. I have been seen in the summer wearing mittens on a breezy day and also inside when the air conditioning is too much for me.

Hope you feel better soon. CRPS stinks!

Shay
Oh it's not a flare-up, it's just the pain that has broken through (breakthrough pain) at an unexpected moment; I call them pain peaks. Normally, I have this a few times a day, but this was an unexpected moment. I get these "pain peaks" sometimes.

No, it doesn't mean the medications have become uneffective. I know. It's just very odd to undergo. CRPS is a strange beast! I know that much.

A flare-up is the whole shebang, discoloration, swelling going on in increased amounts to what has become normal in my chronic stage. And thank goodness it wasn't that bad.

It was "just" the pain. (which is enough)

Thank you for your concern, Shay! I appreciate it.
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All the best, Marleen
=====================
Work related (car) accident September 21, 1995, consequences:
- chondromalacia patellae both knees
- RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008
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