No need to apologize, Christy...it's good to focus on the good stuff!!!...I just posted because we all know how it is...good things, bad things. So many little things are momentously appreciated good things for all of us trach parents. Who would have thought that I would post to "relative" strangers about the wonderful accomplishment of using a walker for example. Our world is just a bit different than most and that's why communicating on this board is such a good thing.
Jakob, born Dec 02, Pfeiffer Syndrome, trached at 5 wks age due to mid-face hypoplasia, cranial vaultx2, monobloc, mid-face distraction, g-tube, pyloric stenosis, nissen, nasal stents, VP shunt, tonsils, adenoids, uvula all removed, tongue suspension, future pilot!!