- Messages
- 2
My DD was diagnosed October 2020 after going into severe DKA and shock she is only 3 and has been put onto the ypso pump with a dexcom. I am absolutely hated the ypso pump but the dsn and consultant really pushed for her to be in it as they told me it was the best one for her and no many options for her age group. She was originally put on the soft orbit cannulas and we were having cannula and tuning fails constantly not one cannula lasted the three days and some didn't last the day they were changed. We recently changed to the steel cannulas and whilst theyve been 'better' we had a box of cannulas with occlusion whilst prepping the tubing and just random blocked cannulas with no warning which when taken out weren't bent or damanged but when we connected it back to its tubing and ran insulin through nothing was coming out she is a small 3 year old with no much fat on her and wears her cannula on her stomach and I'm reluctant with putting it anywhere else. When we were doing MDI she was beautifully in range and now on the pump hardly in range at all maybe over a few days if we have a lucky cannula! Has anyone had the same issues with ypso because I'm really considering going back onto MDI as it seems more hassle than it's worse really and feeling down about it spoke to dsn about it but was made to feel really bad about the possibility of giving the pump back. If anyone has any advice or help it would be really appreciated thank you.