Hi there, and thanks for visiting.
'My Little Health Project' started off in 2017 as a very small instagram page which was intended to help me vent and find other people who were suffering from neurological and autoimmune disorders like my own. I suffer from a rare neurological disorder (which is also linked to the immune system) called Parsonage Turner Syndrome and I have also recently been diagnosed with Intracranial Hypertension. Years ago when I was 18 I was diagnosed with familial Polyposis (basically little tiny growth form in (in the 100's) in your bowel and if they are not removed frequently via colonoscopy you will likely reach an outcome of cancer.
So to say I have my plate full medically is an understatement. I was overwhelmed and wanted to find other people like myself who suffer the same things I do and understand what it feels like. When someone is a fellow sufferer they just seem to get it.
But I was completely blown away by how much support I was receiving from completely healthy, average, everyday people and by ow my the page grew. They wanted to hear my story. They wanted to know where I came from and who I was before the illness took over.
Their love and support has given me drive and it has given me purpose. For that I and truly grateful to every supporter, well-wisher, liker, commenter and love heart -leaver. The best thing about Instagram and Blogs is that I could be having a really good 'well' day and jump on and post and pic or I could be sick in hospital writing a blog. Im not limited for the first time in a long time.
I do hope you enjoy my little Jars that I open each week and if you have any questions or suggestions please don't hesitate to DM me.
Love and Light to you all,
Megan
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