Please help us raise funds for our best friend who is an absolute warrior woman! She is a one in a million with a beautiful soul, full of life, always smiling, loving & caring, laughing and keeping her spirits high despite the traumatic experience she has gone through over the last two years. She is a super single mum of two lovely teenagers who need their mum to be well again and we all desperately need her to get her life back completely!

Somehow she has managed to survive 6 lots of brain surgery, which has left her with serious physical and emotional damage without much success. As times gone by this AVM has been recruiting new veins meaning it's constantly growing.

She is open to the alternative options which she would like to try first before she is made to go down the conventional path of Gammma-knife radiation, which we all know is highly destructive to the body!

This is Emmaline's story from herself;

I was diagnosed on the 7th of April 2017, suffering unknowingly from an AVM. I collapsed whilst i was mowing my lawn on a sunny spring day. They said my brain was under too much pressure (blood flow) so it haemorrhaged which caused the fall in my garden.

AVM medically is known as a ''arteriovenous malformation" or as i call it a mass of spaghetti in my brain. The neurologists said the reason why this has happened to me is the arteries in my brain didn't form properly when i was born.

Since that hideous day, I've had countless mri scans, cat scans and millions of needle prodding and poking around inside my brain. Ive had 3 embolisation's and 3 angiography procedures which is 6 lots of brain surgery in total. So this spaghetti has shrunk slightly but it's still very large so they now want to give me gamma-knife, a form of radiation which I really don't want to go through, as I cant take any more mental, emotional and physical pain.

So Far in this hell of a journey, from the hospital treatment that hasn't done a great deal, I've been left with permanent severe dizziness and also lost my hearing completely in my left side which has given me tinnitus for life. The deafness will never go due to the nerves that were damaged during my 3rd lot of brain surgery. I've also gone through the upset of losing my hair due to the medication that I've been on, which I didn't think would happen to me. On top of all of that I've been blessed with short term memory loss, terrible neck to groin pain on my left side of my body, thanks to all these procedures, which have all been done through my main artery as well as nerve damage in my hands and feet, constant numbness of my left side of my tongue and reoccurring ulcers in my mouth.

I am home now in bed most of the week due to the debilitating side effects of the treatments and side effects of the hospital treatments, although I do put on a brave face for my friends and try my hardest to just be me.

We are raising funds to give Emmaline the opportunity to use an alternative and holistic route of therapy including professional nutritional & detox programme, work on her mindset, deep energy healing, the permanent use of CBD oil and the use of a bio-resonance therapy.

Bioresonance is a non-invasive therapy which involves placing electrodes on your skin for diagnosis and treatment. The electrodes are connected to a Bicom machine which checks the energy wavelengths coming from your body, and then counteracts bad frequencies by restoring the optimum balance.

The hospital specialists have said that if her blood vessels in her brain do burst then it could either leave her badly brain damaged with hospital care for life or fatal...

Emmaline does have a bucket list of experiences she would like to tick off in her life which we would love to help tick off for her just in case her treatments are unsuccessful (we are not believing they will not work!) Although she is very poorly and is suffering daily from being permanently dizziness from the adverse reactions from her hospital treatments. Her passion has always been music and loves to dance where shes always felt her most happiest in her life , she has loved her music festivals and would love to see more of our world. one of her dream's has been to visit the island of ibiza one day, and also would love to visit london to see the musical Wicked..If these proposed treatments have helped shrink to normal size this AVM (spaghetti in her brain) and we have raised enough funds to fix our dear friend.

Please help us save a extra special one in a million good egg!