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Other than meds...What helps you the most?

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Fibromyalgia
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crazykitty
Veteran Member
Joined : Jul 2009
Posts : 4796
Posted 3/23/2011 12:15 PM (GMT -8)
For me, it's a toss up between heat, relaxation therapy, walking, having fun with( hubby, family, friends or on my own) prayer and the fibro family

Other than meds...what helps you the most?

Have a great day :-)

Hugs, Robin

oops...forgot a positive attitude turn

Post Edited (crazykitty) : 3/23/2011 2:23:23 PM (GMT-6)

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bermans
New Member
Joined : Mar 2011
Posts : 15
Posted 3/23/2011 12:32 PM (GMT -8)
What helps me is keeping busy and feeling useful. This morning as usual the worse of the symptoms starts after breakfast. Unless I have something planned I end up going nuts. Today I took and short shower when the cold sweats started. Helped a bit. At least it got rid of the burning on my skin from perspiring. I made Chili in the slower cooker. Chopping all those vegetables and turning Lady Gaga's "Born this Way" up real loud. I thought it might inspire me and get some of that fibro fog out of my head. It was like cotton batten in my ears and brain. After that I yelled at my hubby a bit then did the laundry. LOL. Then I went for a long walk trying to ignore the pulsing pain all over. It was cool but I sat in the park with my face to the sun for awhile. Right now its 4 pm I feel almost normal. That's if DH dosn't cause me more stress. A day in my life. Tomorrow morning I see the Pain doc. Should be a waste of time as usual. I really should find a good fibro doctor. Hope you all have had a good morning.
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Acheybody
Veteran Member
Joined : Nov 2008
Posts : 6036
Posted 3/23/2011 12:51 PM (GMT -8)
People who care, #1 always.

Something interesting to distract me.

Alternating between activity and resting.

And always, always, music. Don't know what I'd do without it!

Debbie
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getting by
Forum Moderator
Joined : Sep 2007
Posts : 45224
Posted 3/23/2011 1:55 PM (GMT -8)
I think for me it is feeling useful too. And walking. I am so looking forward to the end of winter, or at least some of the snow going (we got a ton last night) so I can walk. I think having a positive attitude helps a lot too.

Hugs to all,

Karen
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Witchesblew
Regular Member
Joined : Jul 2010
Posts : 105
Posted 3/23/2011 3:58 PM (GMT -8)
Feeling useful...music (a must), and this board is how i get through my days!
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FibroNana
Regular Member
Joined : Sep 2010
Posts : 194
Posted 3/23/2011 4:00 PM (GMT -8)
Great question..

For me, my prayer time...when I get really bad and even the meds aren't helping....I rest and pray...or think about my new journey of traveling with my Hubby.

my biggest motivator is my Hubby..he helps me get going in the mornings...but also knows when to back off or when to tell me to slow down..

hot baths, listening to music, I love music!!!

I love being able to do household chores even when I don't think I can...and even if it's something small....I feel I accomplished something and that I'm doing my part.

My next big goal is to start walking...the weather is gorgeous here in southeast Texas...start out small and work my way up...

oh and one more...even when I am so wore out and I know I shouldn't ...my grandchildren want to come...I let them...they are my greatest joy!!!



this made me feel better just writing this....

Jerrie
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sotiredoffibro
Veteran Member
Joined : May 2010
Posts : 1556
Posted 3/24/2011 6:40 AM (GMT -8)
For me its laughter, if I can find something to laugh about the pain isn't quite so bad.

Thanks once again Robin for making me think. I sure missed having you around to keep me on my toes.

Gentle Hugs
Shirley
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NotSoCrazyAfterall
Regular Member
Joined : Mar 2011
Posts : 91
Posted 3/24/2011 7:05 AM (GMT -8)
For me, distractions are great but have their own repurcussions. My feet and legs are almost my worst part so putting my legs up or lying down would probably be number one and using a little roller supposedly for your neck but I use it everywhere, Tennis ball therapy & my faithful heating pad would all be #2 :).  Oh!  And hot baths!  Yum!

And actually, sometimes walking when my legs are like aliens can be soothing.
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sagescott
Regular Member
Joined : Mar 2011
Posts : 55
Posted 3/24/2011 6:47 PM (GMT -8)
Hi
A hug and a kiss from my dog tux,always seems to cheer me up.Have three dogs and I would be lonely without them,they always no the right thing to say,lol.


Sage
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scaredofswine
Regular Member
Joined : Oct 2009
Posts : 52
Posted 3/24/2011 10:28 PM (GMT -8)
Prayer, Hot baths, vitamin D, medication wise vicodin when in extreme pain which i'm no longer prescribed :-( although i believe it's probably best to do without that, and great people in this forum.
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ladywithfibro
Regular Member
Joined : Nov 2010
Posts : 454
Posted 3/25/2011 12:43 AM (GMT -8)
Long hot showers help with the pain. For relaxation, my dogs. I have a yorkie (gypsy), a Pom (Seymour), 2 long hair chihuahuas (Puff and Harley). Snuggled up with them in bed makes me feel so good. We even let hubby in the bed too!
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Alcie
Veteran Member
Joined : Oct 2009
Posts : 5177
Posted 3/25/2011 6:07 AM (GMT -8)
Hot tub, heating pad, distractions. Of course the pain always comes back.

Getting rid of other pain - bursitis, spine pain, sciatica, anything that causes me to hold my breath and clench my teeth - with cortisone injections or PT, eases fibro pain. Of course cortisone's medicine too.
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grandmaroses
Veteran Member
Joined : Jan 2011
Posts : 1355
Posted 3/25/2011 6:57 AM (GMT -8)
I really think positive attitude goes a long way. These cold weather and gloomy days are soon going to end.
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Swansonmjs
Regular Member
Joined : Mar 2011
Posts : 100
Posted 3/25/2011 11:11 AM (GMT -8)
For me, water exercises, heating pads, relaxation exercises, the weather being nice and warm, and writing.  It is great when I can do physical stuff with my Daughter or the Girl Scout Troop but I need to schedule swimming after each event.  I have tried the Hot Stone massages - worked great but can't afford it on a regular basis.

Good Luck - Sun is shining in NW Wisconsin!!! smilewinkgrin

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cgk
New Member
Joined : Apr 2011
Posts : 3
Posted 4/4/2011 12:40 AM (GMT -8)

I think that a person has to develop an individualized, multifaceted approach to their symptoms. For me, medication has made the most difference - made my life pretty normal after years of pain and other symptoms. But I also have to do multiple other things - several supplements – Vit. B, CoQ10, magnesium, calcium, chromium, heat in bed at night (electric blanket or mattress pad or water bed,) positioning with pillows when I sleep to allow muscles to relax, Yoga, moderate aerobic exercise – not to exhaustion. Before I was on meds, I used spicy food to help with the pain - spicy Asian foods, flaming hot Cheetos or pepperonicini peppers. Positive self talk is very important for me.

          Dietary things - high protein breakfast and lunch and high carb dinner (rice, pasta - not food high in fructose), avoid some foods - e.g. large amounts of red meat, carbo loading when I'm pre-menstrual, drink alcohol in moderation and drink a lot of water during the end of an evening out (notice if some types cause more problems - for me it red wine and champagne,) Be aware that alcohol is initially sedating, but in about 4 hours it acts as a stimulant which can inhibit sleep.

Make sure my hormone levels are normal - for me that has been finding the right BCP or hormone patch (Triphasal sent me into a serious exacerbation, Ortho Novum pulled me out of it.) Realize that weight gains or losses impact hormone levels (I had a very bad exacerbation when I lost weight and forgot that I needed to increase the dose of my BCPs.)

Keep my back, chest and shoulder muscles loose so I can breathe easily and move my arms freely - my muscles had been so tight for years that when a Yoga teacher gave me exercises to get them to relax, it felt like my arms had become wings! Use an ergonomic keyboard that directs elbows to move away from the body and reduces shoulder tension.

 Learn selective ignoring of the pain, but be careful. I'm so good at ignoring symptoms that when I had an acute appendix, I put off medical care for so long that I was septic before surgery.

When I was prescribed sedating medication - Trazadone and Elavil /amitriptyline (which work very well for me and are inexpensive) I cut up the pills and started by taking a smaller dose than was prescribed and gradually worked up to the dose that was right for me. (I've known other people to give up when the prescribed dose made them too sedated. Note that when you swallow a piece of an Elavil tablet, it might make a numb spot on your tongue for a few minutes, but it goes away. Elavil has topical anesthetic properties and is made with an enteric coating to prevent this sensation.)

Become the authority on your body. Find health care professionals who respect what you know about yourself and will work collaboratively!

Hope I don't sound like I'm preaching. I've lived with FM for 40 years and have learned a lot by trial and error. Hope it can help someone.

Post Edited (cgk) : 4/4/2011 3:40:46 AM (GMT-6)

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Klambert1
Regular Member
Joined : Mar 2010
Posts : 350
Posted 4/4/2011 8:40 AM (GMT -8)
I have alot of hobbies. Scrapbooking, card making, painting, sculpting, and everything else under the sun..lol. They keep my mind off of my pain sometimes. Hot showers/baths helps for awhile. I do try to do something in the house, cleaning, decorating, even to get a room done or the floor mopped is a great feeling. Getting out with hubby is nice, esp eating dinner or shopping, he loves to go with me places. He is so supportive and has been a wonderful husband through all of this. I don't know what I would do without him. I enjoy a few good tv programs and comedy. I have a teacup poodle who is a clown, and we just got a puppy a few weeks ago. SO I HAVE to get up early in the morning to help take care of him..lol. Both are a handful but they are always happy and they never tell me to suck it up and deal with it..lol. Of course resting and learning to balance my energy and what I need to get done. Also being close to God and prayer. He knows everything we go through, struggle with, and all of our pains and sufferings. I know there may or may not be a reason why I have this, even though I don't understand right now, but I know one day we will live without suffering, pain and sorrow, and that is comforting to me. I always say, things could be worse.

KL
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Dagger
Veteran Member
Joined : Apr 2008
Posts : 1522
Posted 4/4/2011 1:32 PM (GMT -8)
Yoga, hot showers, hobbies, reading.
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MeGoSun
Regular Member
Joined : Nov 2010
Posts : 392
Posted 4/4/2011 2:43 PM (GMT -8)
Nice hot bath.
Family.
Keeping busy.
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