My Name Is Meg, I’m 16 Years Old And Everyday I Fight A Rare Genetic Disease Called Ehlers Danlos Syndrome.

My name is Meg, I’m 16 years old and everyday I fight a rare genetic disease called Ehlers Danlos Syndrome. The disease is on a spectrum and sadly I have an extremely severe form of the illness.

I am in desperate need of brain/spinal surgery. Over the past year, my brain has started sinking and causing serious pressure, my spine is collapsing and my windpipe is closing. Without this surgery, I will most likely not live to see my 17th birthday. My main blog is here and as you will see i spend all day every day helping people I have never met. Now I am asking for you to do the same.

I earn money through placing sda (read backwards) on my blog. If you would have the heart to go to my blog, click the ‘shuffle’ button 10/15 times, click the da (read backwards) and keep that tab open for a few minutes, it would help me so much. All the money goes towards surgery and medical equipment. If you would like to help in a more direct way, my boyfriend has created a gofundme here that takes donations - all the money goes to my surgery. 

Please help me, it only takes a few minutes to click and it really could help save my life.