Support and friendship for Australian parents of children with Anencephaly, also offering support to family and friends touched by the loss of a child to Anencephaly.
The rare and devastating Neural Tube Defect known as Anencephaly touches too many people each year, and yet it is hard to find answers and support. This group was created by mums affected by this devastating condition in the hope of helping others through the grief and emotional turmoil associated with Anencephaly.
This group is a private group, you must request membership, it will be granted by the administrator as soon as humanly possible.
As this is a group dealing with the loss of a beloved child, it is appreciated that only genuine applications are made. Grief is a delicate minefield of emotions and a safe haven for expression of feelings is needed for this group to exist harmoniously, please respect the needs of suffering families.
The aim of this group is to offer support and comfort from those who know through experience, regardless of the choices made following discovery of this condition in the pregnancy. We may not always agree with each other's decisions to continue to term or choose termination, but respecting each other's choices is of paramount importance.
Hi Naomi, Sorry that you have needed to join us but I hope that we can help you in some way. I'm not sure why itsbeen so quiet but I am around if you need to
HI everyone, please welcome new member Naomi to our group. Naomi, if you ever need a natter, please feel free to post on the board or you can always email me
HI Jenny, it's lovely to see you pop up and say hi! I am sad to read of the passing of your beloved pooch, big hugs to you. How lovely the image of your
Hello to all our members, I am so sorry I have dropped the ball in the past year and let our group blend into the background in my own life. I have missed a