Whenever either of my wives punched me out, I found that
"Borghese" (sp)
was the best foundation, which of course, was all I used, besides masquara... and sunglasses!

It covered my black eyes, and stood up to some sweating....!
What more could "eye" ask for?

Good stuff!

Macy's!
(Unless it's an emergency, like I had, wait for a sale!)

pete

:^)

Sarah
Ive Rsd about 1yr now, as the disease progresses one symptom during the duration was sweating,,I dont sweat too bad over my affected limbs , but id do under the arms,exspecilly if im worried, and when i do sweat [underarm] it comes with a bad odor,,really bad,, im in pretty good shape,before my accident that caused this mess, I was an active sponsored ball player. Now ive got it in both hips,,its heart wrenching not being able to play anymore,but that is Gods will for now and i must accept this. Any way about the sweating, when i played ball or was working construction,I sweated alot, but there wasnt any smell,just sweat,,Now with RSD stinch underarm comes with the sweat,and as others have commented,Its ussually when im really worried[then i sweat like a pig and fast,it immediate] and its also a precursor to a bad flare,,,,I do know that rsd does effect the vasamotors[sweating]and submotor[circulation]. Oh by the way , I do have RSD 2[causalgia-nerve entrapment] which makes everything with me excell with the disease. And I have ruled out that it was the pain meds,,i like others,switched them around and nothing help, but my most incriminating evidence that it is the rsd,,is Ive on 4 occasions have gone completly[like now] off all meds,,not even a asprin,,and I sweat just the same,,,,,,,,,much luck and hope ,peace to you all,,,,,,,,,,,,,bobber

bobber...

Happy New Year! and that you I just learned something..This goe back to my question a few threads ago...So when we are having a "progression" a flare during these times we experience these uncontrollable sweating episodes??? Did I understand you correctly???

Thxs...KS

Bobber,

I just wanted to thank you for sharing and also let you know that I really relate to the having my active life style disrupted. I used to be very active with sports, hiking, water sports, rock climbing, skiing, bike riding, and horseback riding all before the RSD and now on a good day my physical stamina is only 25% of what it used to be. I still work on my muscles but I have to do low impact and a specialized exercise program and the limited exercises are not nearly the fun of what I use to do exercise. If you don’t mind me asking, how old are you? I'm 27 so for me personally, accepting my physical limitations has been one of the hardest challenges with the RSD. In fact, as far as the limitation acceptance I still find myself going through a constant roller coaster of emotions, like one week I will go into denial again and overdo it and then because of over doing it I get really sore and then I get angry. Like I said this has been one of the hardest parts for me.
As for the sweating issue that I have experienced, I get it all around my hair line but at night it’s like a full body sweat. I also go on and off my pain meds because of the tolerance issue and during this past month I adjusted the meds to see if it would make a difference and none.
Something that you brought up that I found really interesting was the part of the sweats signifying a flare. I will definitely keep a running track to see if that happens with me but really not sure at this point because the episodes just seem so random.