GothicDiva
Member
- Messages
- 8
Hi,
I was diagnosed with T2 about a month ago by my GP. I’ve been prescribed Metformin and my gp has increased my dose to 2000mg. She didn’t tell me what my levels where when my test came back, just that I needed metformin now. She also advised that my vit d, calcium and folic acid were incredibly low, so I was prescribed additional tablets for this. She said I am young (I’m 41), but she’s seen numbers really drop with metformin and weight loss.(There was also another medication she mentioned but she said that would need to be prescribed by the hospital). She apologised that she was unable to give me a timescale for a diabetes education course or an eye test. And sent me on my way telling me to google it. T2 does not just run in my family it gallops. My Mum had it, so did my Grandmother and great grand mother, along with 2 out of 4 of my uncles and at least 1 of my cousins, so she feels there is a strong genetic connection and my genes basically want me to remain in ‘caveman starvation mode’.
I’ve had a couple of phone appt with her since - she’s been checking on how I’ve gotten on with the metformin. It’s not SR and apart from a bit of wind and an incident with a boiled egg I seem to be tolerating it quite well. However since my dose was increased from 1000mg to 2000mg 2 days ago I just don’t want to eat. I’m just not hungry. I know I shouldn’t take metformin if I’m not eating. It feels like a catch 22.
On top of that I’m really really struggling with what to eat - my diet before wasn’t perfect I’ll be the first to admit, heavy on the carbs. I’ve a veggie in the house and two other very picky eaters, I’ve definitely been going for the path of least resistance. I don’t tend to eat a lot or sweet stuff though - (I can take or leave things like sweets and biscuits and often won’t buy them unless darling family mentions it). Will admit to being really bad for not staying hydrated enough and only eating once a day. I had no symptoms what so ever, and it was only picked up on the blood test. I’m so overwhelmed by conflicting advise I’m actually scared to eat anything! I was advised not to get a BG monitor, but after reading advice on here I have purchased one, because my logic is, how am I supposed to know the effects of what I do eat?
Sorry for the rambling and slightly incoherent post, I just needed to vent and hopefully somewhere that is supportive and understanding. I’ve only told my closest family, friends and employer.
Anyway, if you have made it this far, thank you
and any words of wisdom would be appreciated.
I was diagnosed with T2 about a month ago by my GP. I’ve been prescribed Metformin and my gp has increased my dose to 2000mg. She didn’t tell me what my levels where when my test came back, just that I needed metformin now. She also advised that my vit d, calcium and folic acid were incredibly low, so I was prescribed additional tablets for this. She said I am young (I’m 41), but she’s seen numbers really drop with metformin and weight loss.(There was also another medication she mentioned but she said that would need to be prescribed by the hospital). She apologised that she was unable to give me a timescale for a diabetes education course or an eye test. And sent me on my way telling me to google it. T2 does not just run in my family it gallops. My Mum had it, so did my Grandmother and great grand mother, along with 2 out of 4 of my uncles and at least 1 of my cousins, so she feels there is a strong genetic connection and my genes basically want me to remain in ‘caveman starvation mode’.
I’ve had a couple of phone appt with her since - she’s been checking on how I’ve gotten on with the metformin. It’s not SR and apart from a bit of wind and an incident with a boiled egg I seem to be tolerating it quite well. However since my dose was increased from 1000mg to 2000mg 2 days ago I just don’t want to eat. I’m just not hungry. I know I shouldn’t take metformin if I’m not eating. It feels like a catch 22.
On top of that I’m really really struggling with what to eat - my diet before wasn’t perfect I’ll be the first to admit, heavy on the carbs. I’ve a veggie in the house and two other very picky eaters, I’ve definitely been going for the path of least resistance. I don’t tend to eat a lot or sweet stuff though - (I can take or leave things like sweets and biscuits and often won’t buy them unless darling family mentions it). Will admit to being really bad for not staying hydrated enough and only eating once a day. I had no symptoms what so ever, and it was only picked up on the blood test. I’m so overwhelmed by conflicting advise I’m actually scared to eat anything! I was advised not to get a BG monitor, but after reading advice on here I have purchased one, because my logic is, how am I supposed to know the effects of what I do eat?
Sorry for the rambling and slightly incoherent post, I just needed to vent and hopefully somewhere that is supportive and understanding. I’ve only told my closest family, friends and employer.
Anyway, if you have made it this far, thank you
and any words of wisdom would be appreciated.