Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community ever since she was diagnosed with T1D while in college in May 2013. Since then, she has worked for various diabetes organizations, focusing on research, advocacy, and community-building efforts for people with T1D and their loved ones. Sarah is currently the Senior Manager of Marketing at T1D Exchange.
I was just turning 61 when I received an accurate diagnosis, but was misdiagnosed as a T2 twenty years earlier. My two youngest children were diagnosed at 11 and 6 however. They were diagnosed at just three months and four days apart.
I was a bit of an odd T1D. Some symptoms and elevated BG appeared at about 13 and it was somewhat controlled by diet and exercise until I was 15.
Right on my 15th birthday I ended up in the hospital and started insulin. I’m now 58 so I guess type 1 for 43-45 years.
I was. in grad school and had just turned 28. I thought the symptoms must have something to do with exam and paper writing pressure as it was near end of term. Came on pretty suddenly–over a few weeks–and I had no idea what it was. Fortunately my wife mentioned it to my m-i-l, an occupational therapist, and she said “Get him to a dr stat!” This was back in 1983 and the “Type” nomenclature wasn’t instituted yet, though my Dr told me about it by way of explaining that the auto-immune kind doesn’t track with age. So it says “Juvenile type” on my record.
Dx in 1955, age 4 yr, 7 mos. Called Juvenile Diabetes no matter what the age of the person. Tyoe 2 was adult onset. Later I remember Insulin Dependent Diabetes. I have tried to stay fairly educated about Diabetes. I think bc the disease has been nearly lifelong I didn’t note points of change in terminology.
I was 12yo (1975) and our daughter was 9yo (2006) when dx’d. The differences in our initial experiences with T1D were HUGE. I decided to learn the ‘new’ management techniques with fresh eyes, even though I was well-controlled on a pump for the previous 13 years. Now we’re our own support group!
12 years old
I was diagnosed eight days before my 24th birthday.
Looks like so many get it as older kids! I just barely had turned 4.
13
4
I was a juvenile, back when T1D was called juvenile diabetes. I’m glad I was diagnosed at age 5 rather than 25, honestly.
I was 11, my brother was 7 months old & his oldest daughter was 23 months old when we were diagnosed.
I was diagnosed on my 10th birthday. Easy to remember the date
I was almost 11, little sister was 11 and little brother was 16 at our diagnoses.
4
I was 11. this summer I celebrate 59 years LIVING with it. (I have a brother who was diagnosed at 18, and his son was diagnosed at 4. )
72. I’m 77 now. Our oldest son was diagnosed with T1D at age 29. I like to say that I inherited it from him. 🙂
I was just turning 61 when I received an accurate diagnosis, but was misdiagnosed as a T2 twenty years earlier. My two youngest children were diagnosed at 11 and 6 however. They were diagnosed at just three months and four days apart.
8 yrs old
I was 6 years old. 60 year ago in November!
I was diagnosed at age 8 in late December 1962.
I was diagnosed at age 62 on July 2, 2015. Not too many of us older ones
8
I was a bit of an odd T1D. Some symptoms and elevated BG appeared at about 13 and it was somewhat controlled by diet and exercise until I was 15.
Right on my 15th birthday I ended up in the hospital and started insulin. I’m now 58 so I guess type 1 for 43-45 years.
22
1 month before my 54th birthday.
I was. in grad school and had just turned 28. I thought the symptoms must have something to do with exam and paper writing pressure as it was near end of term. Came on pretty suddenly–over a few weeks–and I had no idea what it was. Fortunately my wife mentioned it to my m-i-l, an occupational therapist, and she said “Get him to a dr stat!” This was back in 1983 and the “Type” nomenclature wasn’t instituted yet, though my Dr told me about it by way of explaining that the auto-immune kind doesn’t track with age. So it says “Juvenile type” on my record.
Dx in 1955, age 4 yr, 7 mos. Called Juvenile Diabetes no matter what the age of the person. Tyoe 2 was adult onset. Later I remember Insulin Dependent Diabetes. I have tried to stay fairly educated about Diabetes. I think bc the disease has been nearly lifelong I didn’t note points of change in terminology.
I had just turned 5 and was in the hospital from Thanksgiving until Christmas Eve.
At 57 I was diagnosed as diabetic. Within 2 more years, I was diagnosed type 1.
Diagnosed T1 at 21 years old.
I was 12yo (1975) and our daughter was 9yo (2006) when dx’d. The differences in our initial experiences with T1D were HUGE. I decided to learn the ‘new’ management techniques with fresh eyes, even though I was well-controlled on a pump for the previous 13 years. Now we’re our own support group!
I had just turned 5 in 1957. I was very fortunate to have Drs. Joslin, White and Krall as my early physicians in Boston.
4. (👍 ͡❛ ᴗ ͡❛)👍 Thumbs up to all you 4-year-olds. That was 70 years ago for me . . . . . . during the technological ice age. Biggest first advance was test-tape in 1956, ref. https://www.washingtonpost.com/local/obituaries/helen-murray-free-dead/2021/05/04/7757199a-ace8-11eb-b476-c3b287e52a01_story.html
Diagnosed in 1951 when I was five years old
I was in my early 30s when diagnosed with t1d.was 7 when diagnosed with pre diabetic
I was 3. A few days marked 25 years.