Hello
@AlicePalace,
I saw your first post on this and I wasn't sure how I might usefully contribute. I understand the problem and I've had my moments when I've felt
'why, how, what ... !' - against this daily challenge; but since my T3c is a consequence of the removal of my pancreas to remove a tumour caused by Pancreatic Cancer, I always have the fall back consolation when I'm feeling miserable (or angry) that my D means I'm still alive and have beaten the cancer. I realise that my backstop is absolutely no consolation or use to you.
Yea it's nice to talk to people that get it as they live with diabetes too. My friends dont always understand
I was fortunate enough to get some counselling, which was very therapeutic, talking to and with someone who listened a lot and let me get my rant out into the open; my counsellor knew nothing about diabetes and didn't need to - he just listened and encouraged me to talk with his useful questions. He knew something about cancer and understood my background fear that my cancer might not be fully resolved (I'm now pretty sure that it is!). During the last session he offered ideas that he felt could help me manage my 'angst' when my D was blatantly niggling me. The trouble is telling you what I got out of counselling doesn't help you and I don't know how you can resolve that - other than encouraging you to share those frustrating moments with the Forum members. At least sharing allows you to let off steam, in an anonymous way and might from time to time get suggestions back that lead to reducing, if not fully resolving, some of the daily D challenges.
It can be hard. I find that when I am struggling with my bloods I can feel more lonely as I feel like no one understands
There is no question: it can be hard. The big issue is STRESS. Stress inevitably alters our BG and for most people raises our BG. So getting stressed about our D is, ironically, adding to our BG variability. I also did some "Mindfulness" training which included a huge list of distraction techniques as well as specific ways of calming myself. You can access Mindfulness ideas on line and there are certain useful books with some great ideas. Glycaemic variability is simply bad for us, so anything we can do to achieve flatter graphs on our CGMs is better for us in both the short and long term.
The doctor that prescribes my tablets is at the surgery but doesn't really support me just prescribes the tablets
This doesn't make it right, but I think all GPs are themselves overloaded with increased nos of patients, each needing an increased amount of their diagnosis and consultation time. So the consequence is that few of us get the support that we actually need from GPs and Health Care Professionals (HCPs). Alas, I don't believe there is an easy answer or simple solution; I wish there was.,
My late step-mother, in the 40 odd years that I knew her (she was more a step-grandmother to our children, than step-mother to me), always used to say when her various permanent ailments were disrupting her life: "never mind, there is always someone worse off". Pretty good advice really and saying it brings a more positive mindset to the common daily hassle you and I have because of our D. Then yesterday morning on the earl TV news, there was a reminder to me about 16 yr old Isla Grist, a young lady who was born with Epidermolysis Bullosa (ED). This is an extremely rare skin disease and her life is totally dominated by her ED (see
https://www.debra.org.uk/islas-story). So the next time I'm frustrated by my D I'll try to remember Isla and her constant challenges; this should make my D management trivial in comparison to Isla's problems.
Anyway this long ramble doesn't provide immediate solutions for you
@AlicePalace. Just some observations; and at least keep talking on here about Mental Health issues - there are people listening.