From Teresa
Living with epilepsy for a caregiver is a challenge every day, much more for people with epilepsy, but for me, as my brother’s caregiver for 36 years, since my mother has been missing, it is a great uncertainty.
I have left a whole world of stories aside for this reason. I believe that there is a lack of means to make it possible for the quality of life to improve for both parties, children, parents, caregivers… a good network would be possible together, but the issue requires effort from the administrations and involvement. Families themselves are sometimes overwhelmed by the situation, and they should have that resource, that protection…
I wish you all to have a future full of possibilities.
Teresa.
