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Anyone else with mody

ps Here in Canada (I'm not sure if this is the case in each province or territory) if a member of your family has a confirmed MODY diagnosis, then genetic testing for immediate family members is automatically covered by public health care (even though the genetic testing takes place in Chicago!)
 

Hi there
I was working as a nurse and just very thirsty and tired - seemed to need a lot of 'pee' breaks when I had a routine blood test which identified I had a sky rocketing BSL. I then had fasting BSLs after drinking copious sugar coated drinks - next think I know I was on Insulin! The only twig to MODY was just over 2 years ago I had to change specialists and he took the family history which was, by now, full of Type 1 and Type 2 and pre-diabetics, so we did the DNA tests and sure enough I am so happy to now be - MODY 3
cheers
M-L
 

What a story! So have all of the family members gone ahead to be tested for MODY3? Has their treatment also changed? As I'm sure you know well, any of your siblings have a 50-50 chance of having inherited the same mutation (since one of your parents was a carrier) and the same for any children you may have or your siblings (with the HNF1A-MODY3 mutation) have had... Also, I'm curious if you've noticed certain foods that tend to produce a stronger insulin response than others? Or perhaps once on tabs this is not so relevant for you? Thanks for sharing!
 
See my post re MODY 2 days ago Rodney from Canada. I am looking to see GP for referall to Test and endocrinologist after my hols later this month. Quite by the by - I am visiting family in Canada. Have citizenship through father and I used to live there. It is my Canadian family genes that have disbetes.
 
Happy Travels! And all the best with the upcoming tests. I'm curious to hear why a suspicion of MODY came up? Happy to hear how things go moving forward.
Warmly,
R
 
Just seen GP re possible MODY she seemed to think it could be a possibility as I am so slim, it is prevalent in my Canadian side. But I am not early onset. DX in my 50s - but who knows how long I may have had it as symptoms are so easily ignored and difficult to recognise.
 
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