Guest guest Posted December 23, 2005 Report Share Posted December 23, 2005 It's been a long time that I've visited this group and recently I have been catching up on the postings. I just love this group and love how supportive all the members can be. Both my daughter and I have BPES, along with my father and 2 older sisters. We wish that this group existed during our time! I do feel fortunate that it exists for my daughter. Some of the postings I've read so far is a bit disturbing. There are couple of postings where BPES is described to be a " disability " . Another posting wrote if it is related to Asians or even to orphans. Other postings go as far if BPES is related to the child's weight! I would like to say from experience, that BPES does not discriminate. It is not an Asian, nor an orphan thing. It is not a disability. It is not a cause for low weights in children. Children with BPES are normal children. My daughter and your daugthers and sons are normal kids. And BPES is really nothing. If we emphasize too much on the negative, then we are teaching our children the wrong thing. What BPES is a genetic anomaly. BPES means small eyes. BPES means droopy eyelids. And BPES does not mean our kids will live unhappy, unhealthy lives. I grew up happily with my small eyes and so will my daughter. BPES is cosmetic. I love how there are photos that show different races across the world. From US, Singapore, to Europe, to Australia. These photos and families are our tools to teach our children with bleph that they are not alone and that they WILL be ok. Perhaps what was once a " rare " disorder is no longer true. The growth of this group shows how we are not alone. So please believe in the positive of BPES and show your kids the beauty they possess in those little eyes! Merry Christmas to everyone in this group! Quote Link to comment Share on other sites More sharing options...
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