There is a dilemma we face that could use the help of…….well……someone….perhaps you. With ‘diabetes technology’ at an all time high (pun intended), there are increasing numbers of ways that we as parents can stay in touch with our children to keep an eye on their blood sugar via the cloud, cell phones etc etc to make […]
Tag: DKA
We are looking for crucial data on DKA. PLEASE share this link in any group where there are moms (and dads) of kids with T1 Diabetes. Local Chapters, Support groups, hospital groups, as well as FB pages and other diabetes gatherings. It is crucial that we get a good amount of participants from every state. Please […]
To say the last two weeks have been an incredible journey would be an understatement. I have just learned so much from you all regarding the topic of undiagnosed T1 and being in DKA. The pictures you sent of your children in the hospital upon Dx with DKA crushed, ABSOLUTELY CRUSHED, me. Know that they […]
I honestly do not remember me ever saying ‘why us’ when Kaitlyn was diagnosed. In fact I am sure that we did not say it when Rob was diagnosed either. It’s how you look at things, isn’t it? “Life” comes at us all the time. It has a zillion-and-one things that are really cool that come […]
There certainly has been much activity surrounding DKA Awareness of late and that is a very good thing; the reason will always sting, but good that change could be coming. If we are to make a dent in this awareness, work; a lot of work, needs to get done. I have had conversations all weekend […]
THIS NOTE ADDED ON 8/2/15: I HAVE ENOUGH FOR NOW…..DO NOT NEED ANYMORE PICTURES/STORIES AT THIS TIME. As many of you know, about 18 months ago I began the Child’s Cry for Change campaign which tackled the missed diagnosis of T1 diabetes head-on. Shortly there after, Kim May (a mom from Texas) and I started […]