Fibromyalgia is a hard condition to live with, especially in women, and sometimes the way it affects the life of a person is something to worry about. That is why some people help others by sharing their experiences, giving some useful advice and all that shared on a blog. Nowadays the internet is a valuable tool where people can find lots of stuff to help but it is important to know that everything on the internet is not true.
People have to be very careful about what they read online. And if careful, surfing on the internet is a real advantage. People can find solutions of any type; people can find doctors; people can find others suffering from the same conditions they are. People can find a lot of help, but do it is important to do it wisely.
Some people enjoy visiting blogs, and they find it really helpful. It is actually incredible the amount of patient blogs you can find. You can read about any subject you want - stories, travelling, medical help, love, art, gastronomy, astronomy, or whatever it is you want to research or read up on.
Blogs have an important role and that is sharing and helping people with any kind of necessity. Talking about fibromyalgia, we can find several people trying to tell their stories and share how every single day they have to deal with the condition. All of those people are different, and they have different life styles so that their illness affects them in different ways and they have diverse opinions. These are some of the best blogs about fibromyalgia you can find on the web:
It is written by Kimberley Linstruth-Beckom, and she is from Connecticut. She always had a strong relationship with letters, so it was so easy for her to write about her condition and about what she was feeling. She was diagnosed with fibromyalgia in 2005, but she has been writing for more than 30 years. Her blog started the day she knew she had fibromyalgia, and she also has written some books. In her blog she talks about everything in relation with the condition including sex and recipes.
This blog has some years; it was founded in 1988 by Kristin Thorson. On this site, you can find a lot of information about fibromyalgia, treatments, several studies, lots of news, and it is very complete of information.
Founded by Lynne Matallana and Lee Richards in 1997, two patients of fibromyalgia who were diagnosed in the 90s. It all started with an online chat for supporting people with fibro after they were diagnosed. In the mid 1990s, they saw a lot of doctors and when they came to the fibro world they saw that the support of the illness was pretty poor, so starting by themselves they offered support groups and an online chat. It is a very complete site, where you can find a lot of reliable information like researches, support groups and it has social media, too.
Barbara Keddy, the blogger, is a nurse, college professor and author that has been living with fibro for about 40 years. She is from Canada and where she lives the weather conditions have always aggravated her symptoms, so she has been living with chronic pain. The goal with the blog was that she wanted always to share her condition, because fibromyalgia was treated as if it doesn’t exist. Later, she started to do some social research and found a lot of women with the same problems and saying that they had to pretend the illness doesn't exist, too. In the blog, she offers complete information combined with a lot of experience with fibromyalgia. She also wrote a book.
This is an interesting blog, because it gives you a look from another point - the look from where your loving partner, family or friends stand. They are a pretty important part of living with fibromyalgia. The blog is basically to answer all the questions you have, because people are still confused about fibromyalgia, and they don’t really know if they have it or not.
Shelley, a mom that has been living with fibromyalgia and Lyme disease, has a beautiful purpose. It is to give a little company to sick people, and let them know that they are not alone in dealing with fibromyalgia. She likes to make people laugh, because she thinks laughter is a great medicine. She is from Houston, Texas, and she has two kids. She got diagnosed in 2011, but she has been trying to understand what was affecting her, because her health problems were totally ignored by doctors. So, creating a blog and sharing her experiences was a way out.
Julie Ryan has been diagnosed with fibromyalgia, endometriosis, hypothyroidism, TMJ, migraines and cluster headaches. She offered a blog where she wanted to share her experiences, to let people know that like her, many can deal with everything they have. The blog started in 2010, and the blog has helped her, too, because she learned how to manage her conditions. Many patients have been in the same spot she was in, with no hope because people and doctors believed that fibromyalgia didn’t exist. So, in this blog you can find diets, healthy recipes, medical studies and more people who want to share their experiences.
Donna, the blogger, is from Scotland, and she shares her experiences with Lyme disease, fibromyalgia and chronic fatigue. Like all the bloggers, her principal goal is to help other people, and give company through letters. The blog started in 2013, and the first thing she had on mind was to give people the hope to have a positive life in spite of the different conditions. In the blog, you can find good advice, stories, and a lot of positive content.
This blog is a fairly complete journal where Tamiko shares all her experiences living with fibromyalgia, depression and other things. In her blog, she tells us how she is been dealing with all her conditions, what she learned through the years, and finally based on all that, she gives recommendations.
Support groups and blogs are pretty similar; they share and help others going through similar experiences. Behind these blogs are people that have been putting everything to have a good life, despite their conditions. They know how it feels to live with pain, and they know what it feels like to be rejected or ignored, just because there is great ignorance about fibromyalgia. They know what it feels like to go to the doctor so many times and hear always the same, negative conclusions.
Blogs are used to make individuals feel better, to find answers, to know that there is still a lot to do, and to realize that there are a lot of people like you, trying and looking for something to feel better. See that behind each blog there is a mother, a sister, a husband, a professional, a young woman, an artist, a person like you that is passing through rough times and wants to tell how it is to live with fibromyalgia.
- Support groups and blogs are pretty similar; they share and help others going through similar experiences.
- There are a number of fibromyalgia blogs available to read online.
- Many people have experienced similar, disheartening things when trying to figure out what was wrong with them.