Who is Chronically Hopeful Char?
My name is Charlene. I was born and raised in South Africa, lived in Italy for ten years and now call England home.
Before falling ill I was a Teaching Assistant supporting disabled children and a Teacher of English as a Foreign Language. Now I am housebound, reclined on my bed or sofa, resting, blogging, painting, drawing, watching nature through our windows and raising awareness of invisible illness online.
Why Did I Create ChronicallyHopeful.com?
My main motivation is that I am passionate about raising awareness and helping others. I use this blog as a platform to share information and advocacy resources as well as giving others a place to share their stories and empowering them to raise awareness too.
Also, I am often asked about my conditions and how I manage them, so I decided it would be a good idea to collect all the relevant information in one place I could direct people to.
So, Chronically Hopeful is a place for:
- healthy people to be educated on the struggles of people with invisible chronic illness and hopefully be inspired to help support somebody in their community.
- patients to find resources, support and encouragement as well as ideas on how to adjust to their new normal.
- me to share my personal journey through faith, chronic illness, art, home life and more. A sort of online diary recording my progress as I aim for recovery.
As you can see from theNavigation Menu at the top of each page, I cover a variety of topics which fall under 3 main categories:
- Invisible Illness - all about living with chronic illness - includes tips on how to get by, nutrition for health, guest features and more.
- M.E. Awareness - all about Myalgic Encephalomyelitis - includes awareness pictures to share, advocacy resources and campaigns you can participate in.
- My Chronic Life - all about my life - health, faith, art, home life, blogging and more.
If you'd like to be featured on my blog, visit this page to find out how you can contribute. I would love to share your story here!
I believe that sharing our stories is the best way to raise awareness and eliminate stigma.
There are currently 3 campaigns open: Celebrating Life, Eat To Heal and Faith Through Illness. There's also an interview for carers.
If you prefer to not do a Q&A style interview, I am happy to share your completed guest post at Chronically Hopeful. Do get in touch and let me know what you have in mind!
POF - In 2014 I was diagnosed with Premature Ovarian Failure. It is essentially early menopause. My ovaries just stopped producing eggs and I haven't had a period in years. I had an extremely rough couple of years initially, the menopausal symptoms were intense and constant. It became quite debilitating. I was then put on Hormone Replacement Therapy in 2014 and was doing much better. After 4 years on HRT I decided to ween myself off them and am happy to discover that my menopausal symptoms are not as bad as they were initially. Mainly just a few hot flushes daily.
ME/CFS - In 2015 I was diagnosed with Chronic Fatigue Syndrome. It is a complex neurological disease which affects all body systems. It has had many names over the decades, but is now most commonly referred to as ME/CFS. (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome).
My most persistent symptoms are a complete lack of power to function normally, widespread pain in muscles and joints, profound exhaustion and weakness upon exertion (whether mental, emotional or physical exertion), cognitive dysfunction, unrefreshing sleep, shaking and tremors, tingling pins and needles and numbness of the limbs as well as heart palpitations, breathlessness and sensory sensitivities. These are only the constant companions, there are many more unpredictable symptoms that come and go and they all vary in intensity daily. You can read my ME story here.
I have also been dealing with Histamine Intolerance, self-diagnosed and managed, since the start of 2017. The main symptoms being itching, rashes and hives upon eating or drinking certain foods, accompanied by hot flushes and burning, swollen joints. It is also triggered by heat and sun exposure as well as intense emotions. You can read all about it over here.
Apart from this blog, I have 2 main accounts on each social media platform, one for my blog / chronic life posts and the other for my art. I'd love to connect with you there!
I am a member of the Amazon Associates Programme as well as some other affiliate programmes by companies I trust and use regularly, like Tailwind and Bulk Powders. Affiliate advertising programmes are designed to provide a way for sites to earn a little money by advertising and linking to companies or their products. This means that if you purchase anything after clicking my links, I will get a small reward, at no extra cost to you. Thank you for your support!
DISCLAIMER: Although I only link to products I believe would be beneficial to my readers, I cannot be held responsible for any choices you make. I recommend reading reviews online and coming to your own conclusions before spending money.
Proud Community Member
Below are the badges of some great blogging communities I am a member of. If you are a blogger and would like to meet other like-minded bloggers or need support, visit these great pages!
My Theme & Page Layouts
This blog is running on WordPress using Thrive Themes. They have fantastic tools for building pages and posts, sign up forms and more. Allowing you to personalise just about every aspect of your blog without needing to know any code. They have a brilliant theme builder called Thrive Architect, which is similar to the new WordPress Gutenberg, but way more advanced in terms of capabilities and the variety of tools available as they've been at it for years.
Click here to see what Thrive Themes is all about.