In 12 days, I will officially have had diabetes for more years than not. I remember the first year with the disease, I felt so hopeful and confident that I’d be cured in no time–maybe 5 or 10 years. But now that I’ve reached 11 years of needles and doctor’s visits and blood sugar testing, I realize that I need to finally accept my disease. Please visit my blog  collegeveganista to read on. 

Views: 84

Comment by Brian (bsc) on March 15, 2012 at 4:40am

While oil and water alone don't mix, they do mix in the presence of an emulsifier. Perhaps for you, the acceptance of your diabetes is your emulsifier, and diabetes will become just part of you, instead of it being a separate glop of oil on your back dragging you down.

Comment by Shannon on March 15, 2012 at 7:45am

I hit that mark in 2010 (18 years with it.) It hit me like a ton of bricks that I'd officially lived more of my life WITH it than without it. :/ This year, in October, it'll be my 20 year "anniversary" with T1. I have always been involved with my local JDRF chapter, but just within the last month I have decided to start a blog, and start using my disease for good vs evil. (http://nomoreshotsforshannon.wordpress.com) It has helped to write about it, too, because I don't have any close T1 friends. You're not alone, Leanne! :)

Comment by Timothy on March 15, 2012 at 2:01pm

They told me the "5 year story" when I was diagnosed, 25 years ago. I think they tell doctors to use the "5 year story" whenever possible.
I have decided that no matter how long it takes, it will not be 5 years. Even now If I talk to a new doctor, I get " you know in 5 years this disease wont even exist?" It is all I can do to not punch him. I think it took me a good 5 years to just accept that I have this for ever. I think the new "5 year story" should be: " This will be a rough transition and in about 5 years you will begin to accept that it is for ever "
Once you do that then life gets easier and the disease stops running your life.
( say all this with a blood sugar of 230 because my pump canula came loose)
Just sayin is all :)

Comment by Leanne on March 16, 2012 at 7:55pm

Thanks guys! You're all so helpful and I appreciate the support.

Comment

You need to be a member of Diabetes community by Diabetes Hands Foundation: TuDiabetes to add comments!

Join Diabetes community by Diabetes Hands Foundation: TuDiabetes

Advertisement



REsources

From the Diabetes Hands Foundation blog...

#MedicareCoverCGM Panel Discussion

If you follow the diabetes online community, you know that #MedicareCoverCGM is a big deal. We have continued to raise awareness on #MedicareCoverCGM because we believe that ALL people living with diabetes should have access to continuous glucose monitors (CGM). With Read on! →

#WalkWithD: Making MORE Sense of Diabetes

  A few years ago, we at Diabetes Hands Foundation reached out to the members on TuDiabetes and asked them to share their perspective of life with diabetes through one of the five senses, as part of an initiative called Read on! →

Diabetes Hands Foundation Team

DHF TEAM

Manny Hernandez
(Co-Founder, Editor, has LADA)

Emily Coles
(Head of Communities, has type 1)

Mila Ferrer
(EsTuDiabetes Community Manager, mother of a child with type 1)

Mike Lawson
(Head of Experience, has type 1)

Corinna Cornejo
(Development Manager, has type 2)

Desiree Johnson  (Administrative and Programs Assistant, has type 1)


DHF VOLUNTEERS


Lead Administrator

Bradford (has type 1)


Administrators

Lorraine (mother of type 1)
Marie B (has type 1)

Brian (bsc) (has type 2)

Gary (has type 2)

David (dns) (type 2)

 

LIKE us on Facebook

Spread the word

Loading…

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information: verify here.

© 2014   A community of people touched by diabetes, run by the Diabetes Hands Foundation.

Badges  |  Contact Us  |  Terms of Service