TASHA'S MITOCHONDRIAL TREATMENT

Tasha has been diagnosed with a rare mitochondrial disease.
Which is the primary disease with other rare secondary illnesses.
Tasha is 23. And over the last 2 years. Her life have been devastated by these rare life changing illnesses.
She has gone from being the life and soul of the community, to fighting a personal life limiting battle.
The disease has struck in such a devastating way that she is currently paralysed from waist down, unable to breath unaided and relies on a ventilator and tracheostomy, unable to swallow, and is fed through a tube. Blind in her left eye and light sensitive in her right eye. Unable to support her own head unaided.
Despite all her own medical problems, tasha is still up beat about life and spends her time encouraging other people throughout the world to never give up with there own personal fight with chronic illness.
Since her diagnosis we have found out information from a research hospital in America about a treatment of specialist tailored medication that could improve quality of life and possibly extend life expectancy.
Due to the treatment being tailor made for the patient, it is very expensive.
Tasha has spent all her adult life helping both adults and children, and now needs help herself.
She is originally from Liverpool UK. But now is living on the Costa Blanca Spain and through no fault of her own, is currently not in receipt of any financial benefits from the UK or Spanish governments.

Please try and help a young woman that helps so many.
With your help, she could possibly be given a new, better and longer life.