After years of fighting a heavy battle against Lyme disease, we have to
report that Angelina (mother of two children) has died at the age of
60, due to
Angelina had no money for a treatment. As soon as you are diagnosed
with Lyme in the Netherlands, there is no recognition, help or
reimbursement. In the Netherlands you are left on your own, sometimes
resulting in death. Angelina was so severely disabled over the years
that she no longer was able to come out of her attacks, she was severely
weakened and emaciated.
We remember Angelina as a fighting lady,
who knew very well what was going on in Lyme land. We were allowed to
film her last year of life. She will also be seen in the documentary S.
O. S. Lyme 'the invisible epidemic'.
www.LymeEpidemie.nl
We wish her family and friends a lot of strength.
It's an unfair battle we are fighting. How is this possible in 2018?!
Where is humanity? When does this stop? When will politicians intervene?
Everything revolves about money and power.
No recognition, no treatment and no reimbursement ... How many people have to die ?!
Sign the petition for a good guideline:
https://iladsvoorlyme.petities.nl
Please share! Let the world know the injustice Lyme patients are dealing with..
#Lyme #Injustice #Interests