Lily123
Well-Known Member
- Relationship to Diabetes
- Type 1
- Pronouns
- She/Her
In regards in sending an Email to the diabetes team , I will get one of parents to do that (I don’t have the Email) The chances of me getting a pump may be fairly good as they were very happy to fund the Libre. They said about it at the end of May last year and by early July I had my first sensor!You can get a new pen prescribed. It’s a safety issue to have them different colours. It may take a conversation with the pharmacy to get the colour you want as they don’t always get a say in which come in their orders.
Regarding the pump. Talk to your team. Here (Oxfordshire) funding for over 12s isn’t guaranteed but the team will work out how to give the best argument for funding and get them for all their teens. The process here is that they have info days 3-4 times a year and you go on that first to see what options there are and which you’re interested in and then at your next clinic say you want it and they put the funding bid in. Don’t wait until your February clinic drop them an email this week and start the process to see if you’re suitable for one and if they can get one funded for you. There are lots of benefits to having a pump but they’re not completely stress free. My kid is on another break and back on injections at the moment as he was fed up of it.
Which pump you choose may depend on if you want to self fund for a dexcom or other CGM to link it to the pump otherwise they all have some pros and cons. Here they’re not offering omnipod to new patients but otherwise have a good variety of options.