|Me at 36 weeks|
When I was pregnant with Juniper, I didn't have fantasies about what life with a baby would be like. I knew that life with a baby would be hard. I did have fantasies about what life as a family would be like once that baby got older. I imagined that we'd all go hiking and camping, and to the beach to go surfing together.
When Juniper was three weeks old, we found out that she had a birth defect called lymphedema, and all my fantasies collapsed. There was/is little information about primary lymphedema in babies available, and Daniel and I did not (and still don't) know what to expect. I started this blog as a way to track our life as a family and to maybe help someone else whose baby gets this diagnosis and doesn't know what to do.
This blog won't just be about Juniper's diagnosis though, rather I want it to be about our life: what we do, what's the same as before, what's different, the crafts I do, the beer Daniel brews, and everything in between. I hope that in a year it will be a place where people newly in our situation can come and see that your baby will be fine even with the lymphedema and that your lives can carry on.