Last week I shared, my list of Not your Typical Blogger Awards recommendations. I mentioned in the post that I also had recommendations for chronic illness bloggers that were inspirational and motivating that I would share if requested.
As I continued to reread posts from February of last year, I realized that I had completely forgotten that not only did I actually write a little about MS in February, but I also made a video about being newly diagnosed> I was also fortunate enough to have some of those very same inspirational and motivational bloggers do guest posts on my blog. Their names and links to their blogs can be found here.
I would like to add a few of the chronic illness bloggers that I have also begun following since that post was written that I also find very motivating and helpful.
First is Terri, from Reclaiming Hope. Terri lives with Fibromyalgia, and offers great tips on total wellness, sharing advice on complete wellness encompassing emotional, social, spiritual, occupational, intellectual, financial, and physical aspects. Whether or not, you suffer from a chronic illiness, I think you may find a lot to gain by visiting her site.
Next up is Heather and Dizzy from Dinosaurs, Donkeys, and MS. Heather was diagnosed with MS a only a couple of years ago, but you would think she had been living with MS for a long time, based on the amount of information she shares. Heather shares information about the OMS program, many exercising techniques, and relaxation techniques through her stories with her Donkey Dizzy. She has also begun a podcast featuring two herself and two other MS bloggers from the UK. If you have a minute, potter over to her page, again you will not be disappointed!
Also from the UK is Caz, the author of Invisibly Me. For a quick glimpse at her personality, check out her post, This and That. As with most invisible illnesses, you wouldn’t know that anything is “wrong” with Caz, by looking at her, but she takes this one step further by sharing tips on how she continues to fight and rise above the trials she faces. I especially like her post, What my invisible illness(es) have taught me. If you have another moment, (while you are in the UK :P) take a few steps over to her page. About once a month she will share frugal finds for things she has found that help beat the heat and work on relaxation.
While I’m taking you around the world (well yah the internet is) I’d like to take a moment to visit Vancouver and talk about Amanda from Walk a Myelin* My shoes. Not only does Amanda talk about the realities of living with Chronic Illness on her blog, but she is in the process of writing a book, and often talks about the other side ( caregivers and support people for those of us living with an invisible or chronic illness). To keep in line with the subject I wrote about earlier with being newly diagnosed, I would like to share this post written by Amanda as a place to start.
It is so easy to fall in with “the bad crowd” of people living with chronic illness. By “bad crowd”, I don’t mean bad people, I mean people that spend more time succumbing to their diagnosis and limitations than they do focusing on the positives in their life or are resigned to let the disease consume them. (I think we may all go there from time to time.) Personally, I find it so much more helpful to spend time with people that while maybe struggling, continue to fight each day.
I hope you can take some time to visit the above mentioned websites, and that you find them as helpful as I do!
I have showed you mine, will you show me yours?
Do you have any websites or bloggers that you follow that share tips for dealing with chronic illness? I would love to hear your thoughts
Maybe you can share some recommendations that you have?