I'm the owner of the blog Fibromyalgia Confessions. I decided to make this blog as a way to get information out to all of you. When it comes to living with Fibromyalgia knowledge is power. The more you learn about Fibromyalgia as an illness and about your own personal Fibromyalgia, the easier it will be for you to find a balance in your life. Once you find that balance it's amazing how much easier some things are. Fibromyalgia is painful and will always be hard to deal with but I think we should do all we can to make it as easy as it can be.

Have questions to ask me? Suggestions for blog content or things you'd like to see articles about? Feel free to drop by my ask box!

Check out my other blogs:
Fibromyalgia Confessions
My Personal Blog

Together we can find the balance...

 

The Genes of Fibromyalgia; How it Can be Inherited.

Most of the time Fibromyalgia comes out of nowhere, with no warning or reason. Sometimes, there are things leading up to it, one of the main things they have found a connection with is PTSD (Post Traumatic Stress Disorder.) Studies have shown that over 50% of people suffering from Fibromyalgia went through a trauma that caused them to develop PTSD before they developed Fibromyalgia. But, are there other things? What if our Parents had it? Are we more susceptible to it, then? And if we have it is there a greater chance our children could develop it? Doctors and researchers say yes, there is sometimes a hereditary factor in developing Fibromyalgia.

Though Fibromyalgia is not passed from generation to generation like some diseases are, it does raise the risk of getting it if immediate family members have it. Researchers believe that the reason for this is in the DNA. People with Fibromyalgia have abnormalities in their DNA that is directly related to the nervous system and how it functions. Abnormalities in that can mean abnormalities in the nerves themselves and how they transmit pain signals to the body; that is the case in Fibromyalgia. As most of you know, the chronic pain you feel with Fibromyalgia is due to over-active nerve endings; causing us to feel constant pain and causing us to feel more severe pain than others.

Studies have shown that in families where Fibromyalgia is present, many of the other family members have the same DNA abnormalities. Though, this does not mean all the members of the family with this abnormality will develop Fibromyalgia, it simply means that the risk is higher. It’s hit or miss with this disease, and that makes it scarier. You don’t know if you will develop it if your parents had it and you don’t know if your children will have it if you do; chances are the DNA abnormalities are there, but they can’t tell you for sure if the disease will be passed on. The best thing we can do is be prepared; if someone in your immediate family has this disease then learn about it and understand that there is a possibility that you could develop it. The same goes for if you have it and have children or are planning on having them in the future; you never know so you need to be prepared.

Researchers hope that one day they’ll be able to track the hereditary movement of this disease, but for now all we can do is be knowledgeable about the risks to ourselves and our family members. Like it is with most other things relating to Fibromyalgia: Knowledge is power.

Love,
A.

livingwithdisability:

Have you ever heard of a hands free toothpaste dispenser? 
These are really cheap but so handy.
To read more please click the link below:
http://livingwithdisability.info/handsfree-toothpaste-dispenser/

Great for those of you who get bad cramps or stiffness in your hands; especially in the morning/night!

livingwithdisability:

Have you ever heard of a hands free toothpaste dispenser? 

These are really cheap but so handy.

To read more please click the link below:

http://livingwithdisability.info/handsfree-toothpaste-dispenser/

Great for those of you who get bad cramps or stiffness in your hands; especially in the morning/night!

Anonymous asked
Have you had the opportunity to read what Professor Fred Wolfe has written about the expensive "test" for Fibromyalgia that is currently being marketed by EpicGenetics? You will find his assessment on his blog - Fibromyalgia Perplex - look under "Junk Science-Junk Ethics".

I actually had been following the evolution of that test since it began in it’s medical trials two years ago. At the time it seemed like a promising thing-finally having an actual test that would say “YES! You have Fibromyalgia.” I lost track of it over the last year and I’m glad you sent me this message. It’s sad that this is what it became. Basically, a scam to make money is what it is. They know we’ll pay huge amounts for something like this so they’re taking advantage of it and on top of that it doesn’t seem to be a very conclusive test in the first place. Everyone, be aware of this and other kinds of scams relating to our disease. People and Drs alike will try and sell you expensive cures, tests, remedies, etc. Keep this in mind: If they ever find a test to diagnose our Fibromylagia quickly and conclusively or a cure for it, we will ALL know about it and so will all of our Doctors.

I’ve just recently begun working on my blogs again. The thing is, I’m having a hard time thinking of articles to write for this blog. What are some things you’d like to see on here? Everything on this blog is meant to center around information and management of Fibromyalgia. Let me know what kinds of things you’d like to see on here in the near future. Medications? Tips and tricks? Research progress? Anything like that, just let me know and I’ll start researching and putting together articles. Also, if anyone else would like to write a guest article for this blog just submit it to me and I’ll go over it and get it on here asap.

Love,
A.

What would you like to see posted on here in the near future?

Tomorrow!

Hey everyone,

I’m SO sorry for being absent from my Fibromyalgia blogs for so long. Life has been really crazy and hard for me lately. Thank you all so much for being patient and keeping my blogs on your follow lists. Hello to all my new followers! Tomorrow I’m going to start updating both of my fibro sites again. I’ve got a new article written and nearly ready to post on here and a TON of confessions ready to go up on Fibromyalgia Confessions. So, tomorrow afternoon look for new things on both blogs. Again, I’m so sorry for the long absence and for not doing any kind of updates during it.

Love,
A.

Fibromyalgia and PTSD

Currently the exact cause of fibromyalgia is unknown. There are a few connections Doctors have made regarding the onset of Fibromyalgia. One of the most prominent ones is the connection with Post-Traumatic Stress Disorder (PTSD). It’s estimated that over 50% of people with Fibromyalgia had PTSD prior to the onset of Fibromyalgia. This suggests that there is a connection between trauma or severe stress and Fibromyalgia.

The PTSD varies from patient to patient. There are cases of abuse, war, and death. PTSD is an anxiety disorder that is a reaction to a traumatic event. There have been studies that show evidence of PTSD actually changing the way the brain functions. The thought is that these changes in the brain could cause Fibromyalgia, as Fibro is thought to be caused by a brain function issue.

It’s proven that treating the PTSD can help lessen the symptoms of Fibromyalgia. PTSD, like Fibro, is incurable and simply must be treated indefinitely. It’s thought to be helpful to see a counselor or psychiatrist and to be put on some sort of anti-depressant or anti-psychotic.

All of this is also more of a reason to keep your life at a low stress level. The more emotional strain you’re under, the worse your Fibro will be. Ever notice that when you get really upset a flare-up often follows? This is something that is common in a large number of Fibromyalgia patients. So, do your best to stay calm, learn to relax, don’t worry so much, and de-stress often.

Love,
A.

Fibromyalgia and Seasonal Depression (Edited)

Depression is common in Fibromyalgia patients. Some patients have some form of depression before their diagnosis and many patients develop depression due to their diagnosis. As a Fibromyalgiac, I know it’s hard not to get down sometimes-especially if you’re already prone to being depressed.

The winter months are approaching and with them comes daylight savings time and less and less sunny days. In a lot of you, this will lead to seasonal depression. Lack of sunlight causes melatonin production to become imbalanced in the body. This causes sleep disturbance, feelings of depression, moodiness, etc. Personally, I’ve had seasonal depression all my life. At first I didn’t even understand what was happening to me. But, as I learned more about it I started to find little things that helped control my symptoms and I’d like to share those things with all of you.

-The first thing is, try and get as much sunlight as you can. Get up earlier, open the blinds, and go outside in the sun at least once a day.
-Take vitamin D supplements*-this will help replace the vitamin D you are losing from lack of sunlight.
-Make sure you keep exercising. Even though it’s harder to keep up physical activity in winter due to bad weather and increased pain it’s still important. Exercise not only helps fibro pain but it also helps the body produce Serotonin and Norepinephrine-the hormones you need to be happy.
-Take melatonin supplements.* Melatonin is a chemical in the body that is produced while we sleep; it is also one of the chemicals that helps us sleep. Lack of sunlight can disrupt the melatonin cycle. The idea behind taking melatonin is to fix your sleep/melatonin production cycle. Your body needs to know when it should have more melatonin and when it should have less.

I’m not saying that these things will cure your seasonal depression but they definitely can help alleviate your symptoms. The worst thing you can do is do nothing. These things aren’t meant to replace any anti-depressants you may be on, if you do take an anti-depressant use these tricks in addition to your medication.

Many people, especially those who are prone to Depression or those who live in areas where winters are long/harsh may develop serious Seasonal Depression (Which is technically called Seasonal Affective Disorder, by the way, but I never use that term-Sorry.) If your Seasonal Depression is to the point that it is causing serious disruptions in your day to day life you should see a Dr. You could possibly need medication or light therapy.

*Before taking any vitamin supplement check with your Dr to make sure they’re safe for you to take. Also, check with your pharmacist to make sure they won’t react badly with any medications you may be on.

Love,
A.

The Stages of Adjusting to Chronic Illness

This article by Sandy Robinson is a great look into the different stages we go through when trying to accept and live with our chronic illness. Chronic illness isn’t something that is easy to accept, it changes us and it changes our lives. We get mad, we get sad, and we grieve for what we’ve lost.

Hey everyone…

I’m so sorry I haven’t been posting a lot of stuff on here lately. I’ve been in kind of a funk with winter coming and all. I’m going to start posting more frequently though! Also, thank you to everyone who messaged me and let me know the kinds of things they’d like to see on here. It was really helpful!

Love,
A.

What kinds of things do you guys want to see on here?

Tell me what you want, I need some suggestions! Anything related to fibro; living with it, medication, treatments, Drs, research progress, tips and tricks, etc.

Put it in my ask: www.fibromyalgiabalance.tumblr.com/ask

Love,
A.