13 answers

Fibromyalgia - Finally Diagnosed!! Any Advice?

You may have seen my previous posts - In July I was misdiagnosed with Lyme disease and have been undergoing tests since. On Friday I was diagnosed with Fibromyalgia and now I want any advice on how to deal with it.

I'm in lots of pain and can't sleep and I'm always tired. On top of this I suffer from migraines and restless legs for the past 16 years.

What can I do next?

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I can send you some files about this. Just email me at ____@____.com's actually a lot easier to reverse than you can possibly imagine! I know many people who have.

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My mom has Fibro, (along with Rhuematoid arthritis) and I showed her your post. This is what she said...

"She should go to arthritistoday.com-they also have message boards and info on fibromyalgia. there is also a new drug for it-i think it's lyrica ? and there are support groups-she would have to check in her area. exercise, and rest-budgeting her time!"

I am so sorry to hear of your diagnosis. I know how painful can be just by listening to my mom everyday. Please ake care of yourself.

good luck!

After reading your question, it got me thinking if this is what I have. I was tested for lupis and rheumatory arthritis. The tests came back negative. I have numbing pain in my feet and hands and pain in my knees. I don't sleep well because of the pain. I have migraines all the time and I am very very tired all the time. Oh course my doctor blames me being tired because I have a 3 year old. How were you diagnosed? Maybe you can help me. Hope you are feeling better.

Dear friend,

I have a neighbor of mine with fibro. and arthritis. She is a nurse. I told her about a natural product I was taking (I have MS). She has been on it for about two months now and she still can not believe that her pain has been relieved. It all has to do with the inflammation.

It truly works. It is truly the best out there. That is why my life's mission is now to share it with everyone.

I know you are in pain and it does not seem fair. Hang in there. My thoughts and prayers are with you. Feel free to contact me. C.

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I knew it! Didn't I say Firbo? You poor, poor thing. I have several friends with it and man does it suck. The previous poster was right - the key is finding good doctors who understand it and getting proper treatment. Everyone I know who has it still have happy, productive lives.

My stepmother had her calicium levels checked in conjuction with her fibro diagnoses,,,,they were really high....maybe you could be experiencing the same...good luck.

I also have Fibro.
first of all, find a GOOD doctor who actually believes it exists. They will help you through all of it.
My doctor has given me muscle relaxers and pain medicine whic have helped me tremendously. But your doctor can decide what is best for you.

Another thing that helps is massage and pressure point work. It hurts like crazy when it's being done, and you may feel bruised for days afterward, but the rewards are worth it.

Be prepared for more pain when the weather is colder and the air changes. For me, it starts around the first of August.

Get plenty of sleep and don't over do it!! That will be the worst thing you can do to yourself. There will be days when you can do more, but on days when you can't do not feel guilty for it....it's your body telling you to slow down.

There is a theory out there called the Spoon theory.
It goes, you only have so many spoons to use during the day. Each time you do something it uses a spoon... showering for example may use one spoon. Cooking may use one, grocery shopping may use 3.
If you only have say 6 spoons to use for the day, you have to decide what is important to do and how to use your spoons so use them wisely.

If you look at the website fibrohugs.com you can get a lot of information, and you can read the spoon theory for yourself.

Be sure to write down any questions you have for your doctor. Don't be afraid to ask questions.... there are many many symptoms to this stupid, unfair disorder. Be open and honest with your doctor so he can help you.

Oh, for the migraines, do you use a lot of sugar free stuff? If so, you may want to try to go off it for a while and see if it helps... my sisters and I all have fibro and none of us can use sugar free (things with aspartame or nutra sweet) in them because it gives all of us migraines. Splenda seems to be ok, but I just watch my sugar consumption and use regular old sugar myself.

Eating healthy will make a difference too. And drink a lot of water.

Good luck.

Hi!
First, I truly feel for you. It is no fun to be in your shoes.

Second, some attribute fibromyalgia to an overload of toxic chemicals in the body. I can help you if you want to detox.

Third, fortunately, fibromyalgia is not progressive and does not lead to other serious diseases or destruction of body tissue.

Fourth, you might want to have your serotonin and tryptophan levels checked.

Fifth, you probably need to keep yourself limber by doing some simple stretches and flexing. If you can exercise as well.

Sixth, a healthy diet (high fiber, low fat) along with nutritional supplements have been known to help. Eat as many raw fruits and vegetables, whole grains, raw nuts and seeds as you possibly can. Eat skinless chicken, turkey or deep-water fish. Drink fresh juices, herbal teas and lots of water. Eat 4-5 small meals daily. Do not eat anything fried, animal fats, sugars or drink alcohol, caffeine or soft drinks.

Seventh, have you tried alternating hot and cold showers? Studies have shown that cold showers are beneficial for relieving the pain of fibromyalgia. I have also soaked in a tub with a cup of dissolved Epsom Salts.

Please call me at ###-###-#### for further information.

L.

I have had symptoms of Chronic Fatigue for many years, and have found help from my nuritionist, Dr. Herbold ###-###-####. He has a full nutritional program that is individualized from blood and urine lab testing for deficiencies and toxicities. CFS and Fibromyalgia sure aren't fun; what's worse is not being able to enjoy your children as much as you'd like - I know! Best of luck in your journey.
K.

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