We have some great caregiving blogs to share with you this month. They’re diverse and each of them is relatable in its own way. And all of them is trying to help out those who may be affected by their diagnosis or provide information in general.
Swallow My Sunshine should be read from the beginning. This blog is written from the perspective of a mom with a daughter whose diagnosis took years to fully determine. The daughter is well now, but there are some scary moments when reading through the past posts. And the author, Debi Lewis, has a wonderful writing style – and she hasn’t even written up to the present day. She takes you on the journey from her medically complex infant who had heart surgery at 13 months, to her now 10-year-old daughter who is living for the first time without medical intervention.
This blog has a very interesting perspective. It’s written by a man, “Silverfox,” who has Lewy Body Dementia, or LBD. He writes about his difficulties with the nighttime, with having the television on, with keeping his sense of self alive. It can be a depressing read, but at the same time it’s refreshing to learn more about someone who has faced the facts and is simply moving forward.
The Huffington Post is a very popular website – but did you know there’s a section for readers over 50? This “Post 50” section discusses issues relevant to adults in middle age and beyond. The majority of family caregivers are women over 50, and so these articles may just be the right mix. Today, for instance, the top three stories are about dating in middle age, how to find self-identity after the loss of a spouse, and an author’s decision to stop drinking. Keep in mind that it’s still part of the Huffington Post, and so there is a lot of “click-bait” happening, or sensational article titles that attempt to lure readers in. But overall, the articles are thoughtful and interesting.
It’s a new year! Is one of your resolutions to read more? Blogs are a great way to connect to your community and get inspiration. Check out these blogs and sites that provide wonderful stories from various contributing authors:
BLOOM is a Canadian site that is more than just a blog. It’s a magazine, blog, e-letter and speaker series that speaks to parents and caregivers of children with special needs. The new stream of content is fairly steady because those parents and caregivers are often the ones creating the blog posts.
There has been some controversy about The Mighty (see The Cute Syndrome’s blog post for more information about the special needs community’s complaints), but clearly its 80 million readers must find it intriguing. This site gives a voice to those living with disabilities, disease or mental illness, and their caregivers.
Another platform for caregivers, but this site also publishes contributions from those who have Alzheimer’s Disease themselves. It also provides news about the latest Alzheimer’s research, along with keeping the community up-to-date on fundraisers and studies. While the site is sometimes updated as little as once per month, there is a huge amount of information and a backlog of great blog posts.
As the holidays make everyone busier, it’s hard to find time to just settle in and read a few great blogs. But blogs can be the perfect length to read during a quiet breakfast, or during your public transit commute. Let’s take a look at a few of the blogs we’ve been reading lately:
Fifty Shades of Dementia
This blog is written by two British sisters about their parents, both of whom have had dementia for the past several years. Their mother just passed away in September, which they wrote about in a beautiful post. They manage to add humor into their posts, along with giving good advice while chronicling their journey.
The Cute Syndrome
Hillary is the mom and caregiver to Esmé, a four-year-old medically complex child. The title of this blog comes from Hillary discussing Ezzy’s condition with a friend, and how the doctors were telling her that her daughter had a syndrome. “Yeah, a cute syndrome,” came the response from her friend. Thus was born not only the name of the blog, but also the foundation to help children like Esmé.
This site is not only a blog, it’s a community. The site is run by Liz O’Donnell, who has balanced being a caregiver with her other roles in her life. There’s lots of different resources on the site, and it is updated regularly.
As we get further into fall, we thought it might be a nice idea to highlight a few blogs that you can bookmark to read as you settle into your favorite comfy chair with a mug of cocoa.
Noah’s Dad Noah’s parents were surprised when their son was born with Down’s Syndrome. Noah’s dad, Rick, immediately started journaling their story. The blog is full of positivity and super-cute pictures of Noah. There’s lots of advice available for parents of children with Down’s Syndrome, other children with special needs and typical children.
This post hasn’t been updated in quite some time, but it still is a great resource for anyone looking for information about how to improve the lives of geriatrics, especially those with disabilities. There are lots of links to sites with great therapeutic suggestions.
Gastroparesis Crusader Trisha Bundy describes herself as, “a proud mother, teacher, Gastroparesis Advocate, GJ Tubie.” Hers is less a caregiving blog and more of blog from a caree point-of-view. Even with the invisible illnesses Trisha struggles with, she maintains a positive attitude and her writing is very creative.
Wow! We’re already well into summer, but before it passes us by, we’d like to take another moment to highlight a few caregiver blogs that we’ve really been enjoying lately.
The Cute Syndrome
Hillary Savoy decided to call her blog “The Cute Syndrome” because while she was discussing her daughter’s un-diagnosed genetic disorders and various syndromes with a friend, the friend commented, “yeah, she has a syndrome. A cute syndrome.” And the pictures of Esme on this blog are really very cute. Hilary has also written a book about her journey with Esme through the world of genetic testing that is available through her site.
Kate Leong’s tale is one of both sadness and hope. Her first child, Gavin, was born with some disabilities, exacerbated by bouts with both Botulism and Respiratory Syncitial Virus (RSV) while he was still under six months of age. Kate continued to write about Gavin and the therapy he received for his special needs, along with his younger brother, Brian – until Gavin’s death in 2013. Since then, Kate’s blog has focused on the grief and happiness that has come with her son’s death, and her new daughter Hope. While her current story is just as compelling as her past, her older blog posts about Gavin’s therapy may be helpful for those with special needs children of their own.
A new month is here and we’d once again like to take a look at blogs that show us the compassion and grace that caregivers give to their carees.
Jane is the mother of Nicole, who is 20 and has a congenital heart defect and pulmonary arterial hypertension. She’s been writing for four years about her journey with Nicole, Nicole’s health issues and their life together. Recently, she started on a series where she remembers the days when Nicole was first receiving her diagnosis of pulmonary hypertension.
It’s been over five years since Karen’s son, Gavin, passed away, but Karen and her husband, Adam, continue to give their lives to helping children with special needs. They’ve adopted three special needs children since Gavin’s death, with issues that vary from cerebral palsy to feeding tubes. While Karen hasn’t updated the blog recently, it’s full of lots of amazing stories about their journey as a family.
Shelley Webb is a RN and has been a caregiver. She is the “Intentional Caregiver” of her site, which is much more than just a personal blog. It provides care to the caregivers and gives lots of advice. Shelley has other authors that contribute to the site, and has an extensive question section with lots of tips about how to handle various caregiver situations.
Do you have a caregiving blog that you’d like us to highlight? Let us know in the comments!
The Internet has proven to be an enormously helpful resource to parents. Especially to parents of special needs children, whom have created communities of support and sharing. In this blog post, we’ll take a look at all the places all over the ‘Net that can help out parents of children with special needs.
Mashable has less articles for parents of special needs kids, but they’re quality, and there will likely be more in the future
Some local papers and magazines have special needs sections, but the one on L.A. Parent’s site is particularly commendable
Love that Max is written by a mom raising her son, who has cerebral palsy
Chasing Rainbows was started to keep this mom’s family updated on her son, Gavin, who had an un-diagnosed genetic condition. Gavin has, very sadly, since passed away, but her blog remains a resource for those with special needs children