Hi all,
Sorry I haven't posted in a while but been through a rough time and have been in hospital for a long time.
A year ago I collapsed at work and ended up with weakness on right side, weaken muscle in right eye, balance off, coordination off with hands and walking, non epileptic seizures and stroke like episodes.
Since then, three weeks ago I was diagnosed with a rare form of mitachondrial disorder, a rare form specifically called MELAS. This links to diabetes as it cause it and stops the pancreas working. I have no family with diabetes and suddenly developed it when I was 27.
When I was first diagnosed with diabetes five years ago and I was told they're type 1 and type 2 and some sub types in the middle, this is one of them.
The reason for this link is to raise awareness of it, as its rare and the general public and some health professionals are not aware of it and if this posting can stop someone else going through the year I have of being through great. I've had to moved between hospitals and professionals who were unable to help me and I'm having to justify what's wrong as well as not having a diagnosis.
I have to see a specialist in Newcastle this week to see what I need to do to manage the condition, so wish me luck with that.
As for the diabetes, I currently inject 7 times a day, twice with long acting and the rest with the short acting. Its been suggest about an insulin pump. I don't know anything about them. Can anyone help ?
Please read this link and pass the message on about MELAS to raise awareness. 🙂
Cheers
Sorry I haven't posted in a while but been through a rough time and have been in hospital for a long time.
A year ago I collapsed at work and ended up with weakness on right side, weaken muscle in right eye, balance off, coordination off with hands and walking, non epileptic seizures and stroke like episodes.
Since then, three weeks ago I was diagnosed with a rare form of mitachondrial disorder, a rare form specifically called MELAS. This links to diabetes as it cause it and stops the pancreas working. I have no family with diabetes and suddenly developed it when I was 27.
When I was first diagnosed with diabetes five years ago and I was told they're type 1 and type 2 and some sub types in the middle, this is one of them.
The reason for this link is to raise awareness of it, as its rare and the general public and some health professionals are not aware of it and if this posting can stop someone else going through the year I have of being through great. I've had to moved between hospitals and professionals who were unable to help me and I'm having to justify what's wrong as well as not having a diagnosis.
I have to see a specialist in Newcastle this week to see what I need to do to manage the condition, so wish me luck with that.
As for the diabetes, I currently inject 7 times a day, twice with long acting and the rest with the short acting. Its been suggest about an insulin pump. I don't know anything about them. Can anyone help ?
Please read this link and pass the message on about MELAS to raise awareness. 🙂
Cheers