Hi, my name is bon_gil!
I was diagnosed and have lived with ET first in my RH and now both hands plus internal tremors. Add to the mix type 1 diabetes and having to inject insulin multiple times a day and a chronic eye condition caused by diabetes in both eyes with ongoing treatment over the next three months. I am 62 and a carer for my 84 year old mum with a husband who is often working away from the house. I am trying to find others like me who may have developed coping strategies for giving injections. My gp was really unhelpful.
Comments
-
Hi and welcome to the community I'm doing some research in Type 1 Diabetes in children and young people so even though I don't have the condition myself I can sympathise with you.
Another thing I wanted to recommend to you is starting off in the games den and coffee lounge where you can relax.1 -
Hi @bon_gil - & welcome to the community. There seem to be some injection aids which may be helpful. Perhaps you can discuss your need for something to assist you with a diabetic nurse or make an appointment to see a nurse at your GP surgery.
For now you might be interested to look at the following:
1 -
thank you both.
1 -
You're very welcome. Kindly let us all know how you get on.
1 -
will do
1 -
Hey @bon_gil, welcome to the community 😊 I'm glad you've already received support from some of our other members 🙂 I hope you have better luck with a diabetic nurse or asking for specific aids than your first attempt with your GP.
Can I ask, has your mum's house received any adaptations at all? Do you live there as well? I'm just wondering if you've had an assessment of the home to see if there are any other adaptations that could help you or your mum.
Please do keep us updated with how you get on getting those injection aids
1 -
hi Jimm_Scope
Thank you for welcome. I do live with mum. We moved to our current home after my dad died and mum realised that she was more vulnerable in her home. We had the adaptions put into the new house before we moved in and mum has settled in well. I am going through what I hope will be short term loss of vision over the next few months due to having different eye surgeries in each eye more or less at the same time. If all goes to plan I should have more vision in both eyes than I have had for the last year.
0 -
So there have been adaptations for her, but were there any considerations for adaptations for yourself? I suppose if the loss of vision is temporary that may not be considered, but I suppose it couldn't hurt to ask?
1 -
I do intend to ask. I am due an annual review with diabetic nurse so will start there.
0 -
let us know how your annual review goes. We all love to hear updates from members
1 -
Will do
0
Categories
- All Categories
- 14K Start here and say hello!
- 6.7K Coffee lounge
- 57 Games den
- 1.6K People power
- 78 Community noticeboard
- 21.6K Talk about life
- 4.9K Everyday life
- 36 Current affairs
- 2.2K Families and carers
- 814 Education and skills
- 1.7K Work
- 411 Money and bills
- 3.3K Housing and independent living
- 857 Transport and travel
- 650 Relationships
- 58 Sex and intimacy
- 1.3K Mental health and wellbeing
- 2.3K Talk about your impairment
- 842 Rare, invisible, and undiagnosed conditions
- 888 Neurological impairments and pain
- 1.9K Cerebral Palsy Network
- 1.1K Autism and neurodiversity
- 34.9K Talk about your benefits
- 5.5K Employment and Support Allowance (ESA)
- 18.2K PIP, DLA, and AA
- 6.2K Universal Credit (UC)
- 4.9K Benefits and income