So your having a flare up....what are your big guns?

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Hopegirl
Veteran Member


Date Joined May 2008
Total Posts : 704
   Posted 9/30/2008 9:57 PM (GMT -7)   
 
I'll go first, when I have a flare up and it is bad I am getting out the Percocet. It keeps me up but it is the only thing that I have that will even think about getting rid of any pain that I have. Sometimes I will take a muscle relaxer too because at that point all I want to do is go to sleep and hope for the best. I could sure use some biofreeze right now, I'm fresh out. Hubby is sleeping maybe I can sneek some Ben Gay on and he woun't notice???? idea
 
 
Monica
 
Fibromyalgia, Anxiety, IBS, Reflux, Insomnia,
Lyrica 200Mg X2/ Zolft 150 Mg/Ambein CR/Zantag (presc strength)
Taking it one day at a time.... 


Marlee2
Veteran Member


Date Joined Aug 2007
Total Posts : 6067
   Posted 10/1/2008 7:32 AM (GMT -7)   
Hmmm, I've got some samples of biofreeze but have never tried it.
 
When things get bad I get the TENS unit out and moist heat.
 
luv and hugs
Marlee
Forum Moderator Fibromyalgia
 
Fibro,Sjogrens, Anxiety, Gastroparesis, IBS, Gastritis, Allergies, High Blood Pressure, Low Blood Sodium and Osteoarthritis
 
Amitriptyline, Celexa, Xanax, Synthroid, Zyrtec, Micardis, Spironalactone, Tylenol, Reglan, Lidoderm Patches and Tramadol
 
Co Q 10, Super B Complex, Extra B12, Multi vitamin


groaner
New Member


Date Joined Sep 2008
Total Posts : 14
   Posted 10/1/2008 9:23 AM (GMT -7)   
I did not realize that fibro had flares.
I know my lupus does but I have always been under the
impression that fibro stayed at the same level of pain
all the time.
And to think I actually asked a doctor if fibro flared and
she said no.
Good to find this out as sometimes my pain is terrible and
other times tolerable.
That is except at night and then it is just awful.
**Peggy**
Lupus, Parkinson's Fibromyalgia, Diabetes, DJD,
Degenerative disc disease, Osteoarthritis, Osteoporosis,
Peripheal Neuropathy, Migraines, Gerd.


Sherrine
Forum Moderator


Date Joined Apr 2005
Total Posts : 17095
   Posted 10/1/2008 9:55 AM (GMT -7)   
I use my ibuprofen and Tylenol more frequently and lots of moist heat and hot showers.  I do light stretching throughout the day.  I get as comfortable as possible and usually get on the computer and focus on other things and that helps me take my mind off the pain.  I don't have to move much when I'm surfing the net or doing genealogy on line. 
 
Nighttime is the worst for me, too.  When I first lie down I'm nearly groaning but then I do Lamaze breathing and stretching while lying down and that helps relax the muscles.  I have a pillow behind my back so I don't lie flat on my back.  That makes me worse.  As the night progresses and I have gotten some rest, the pain is better. 
 
I do have Vicodin in the medicine cabinet but have never taken one yet.  I try to "gut" it out and have succeeded...so far.
 
Sherrine
Forum Moderator/ Fibromyalgia
***********************
Fibromyalgia, Crohn's Disease, Ostomy, Diabetes, Autoimmune Inner Ear Disease, Osteoporosis
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
God does not give us a spirit of fear, but of power and of love and of a sound mind.    2 Timothy 1:7


getting by
Forum Moderator


Date Joined Sep 2007
Total Posts : 40574
   Posted 10/1/2008 10:25 AM (GMT -7)   
I usually just ride it out. I sometimes go to bed and sleep. I can take extra pain meds if I have to. Also the bed buddy helps. The moist heat really makes my muscles feel better.

I, like Sherrine, try to distract myself from the pain if I can. That isn't always easy, but with concentration, it often works. There are so many different methods of trying to relieve the pain, if one doesn't work, I try another. But in the end it seems like I end up just riding it out until things get better.

Have a great day all.

Hugs, Karen
  Moderator-Depression and fibromyalgia
 
fibromyalgia, Chronic fatigue, depression,allergies


kmhayes
Regular Member


Date Joined Nov 2007
Total Posts : 346
   Posted 10/1/2008 3:52 PM (GMT -7)   
well, if I am just having a minor flare ( few days) I go for the extra aleve, more hot showers...and beg the hubby for back rubs and the like... but I am having a major flare, I head to a massage therapist- I tend to get incredibly tense whenever I have a flare, so along with the pain, I get to stiff I physically can not relax my body....I try to get 1/2 of the massage trigger point release, and the other half just relaxation. If I was a rich woman, I would get a massage once a week regardless of how I felt!

          Kelly


Jokat
Regular Member


Date Joined Feb 2008
Total Posts : 278
   Posted 10/2/2008 5:57 AM (GMT -7)   
I ignore it and try to get out and be active. Adrenaline seems to be a decent pain reliever for me......

JoKat
 
Fibro is a life sentence, but not a death sentence.
Fibro since 2005


Jeannie143
Veteran Member


Date Joined Apr 2004
Total Posts : 6056
   Posted 10/2/2008 9:24 AM (GMT -7)   
Kelly,
I once got massage every week for a year. Bargain basement cost of $1000 that I paid in advance so I had to go. My therapist also has fibro so she understood perfectly. I ended up giving the last of my sessions to my pregnant daughter to help with her pain and fatigue. Although I felt better for a bit each week I have to say that a session in the hot tub at the YMCA was just about as beneficial as the massage. It's a temporary fix and then you are back to square one, at least for me.

Jokat, you are such a guy!!! When my brother's arthritis is flaring he rides his bike about 35 miles! I don't think I will ever understand men! rolleyes
~ Jeannie, Forum Moderator/Diabetes & Fibromyalgia
I know God will not give me anything I can't handle. I just wish that He didn't trust me so much. ~Mother Teresa

"People are like stained glass windows: They sparkle and shine when the sun's out, but when the darkness sets in, their true beauty is revealed only if there is light within."- Elizabeth Kubler-Ross

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