Endometriosis, Family Life and Me
Endometriosis,
Family Life and Me is my way of saying a big "Thank You" to
my family and friends. To my Mum for keeping such a brave face even though
your eyes and voice say otherwise. To
my Sisters and Brother for being so supportive, loving and understanding.
To my Husband
for making me believe that dreams do come true. To my Daughter for
teaching me how to laugh again. To my Friends for patiently waiting
for your e-mails and finally to my fellow sufferers; knowing you
are out there has been a great source of inspiration.
This site is also a tribute to the tireless efforts of charitable organisations
like the National Endometriosis Society and indeed to any organisation out there
providing compassion and support for the sufferers and their families of the
many diseases that
invade our world today.
The information offered here will
hopefully serve not only current sufferers, but those who maybe be curious
about the condition and want to know more or those in the situation I was
in many years ago when I was first diagnosed and knew nothing of the
condition and was desperate for information.
I have also written my story. The story starts from when I was first
diagnosed to present day and how I have (hopefully) grown from what I term
as an 'Endo victim' into a wife and mother.
Whatever reason brought you here today; I thank you for dropping by.
Disclaimer
Please
remember that the contents of this site are for information purposes only
and based on my personal
experiences and not intended as an endorsement of any kind.
Angela Chalmers
Send me an E-mail
