Natasha Bowlds's Page

Latest Activity

Natasha Bowlds replied to Cocheze's discussion 'Alarm won't go off' in the group OmniPod Users
"We use the meat tenderizer."
yesterday
Natasha Bowlds commented on Rob's group 'Dexcom Users'
"EMLA cream - that's what my son uses for the sensor insertion"
May 11
Natasha Bowlds replied to Erik's discussion 'Shifting to a longer transition for existing customers... and abandoning "fair"' in the group OmniPod Users
"ugh - September for us. The sad thing is that the smaller pod and integration with Dexcom were "just around the corner" four years ago when we got it."
May 6
Natasha Bowlds replied to Aidan's Mom's discussion 'Lost, 1 week post T1 diagnosis' in the group parents of kids with Type 1
"We are at Mt. Washington as well. I have heard some not so good stories from Children's in DC - apparently from one main endo. I know two other people who have switched from one to the other."
Apr 30

Profile Information

How do you hope to benefit from TuDiabetes?
support
Date diagnosed
September 21, 2008
Most recent HbA1C %, date of result (optional)
7.2
Type of treatment/devices you use
Pump
What pump model do you use, if any?
Omnipod

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Comment Wall (14 comments)

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At 8:43am on August 22, 2011, Linda G said…
Bravo on being a featured member Natasha!
How is Sam doing? What grade will he be in come September??
At 3:06pm on April 15, 2011, Trev said…
Hey, Thanks for the friend add! I have been unplugged for a while, well on weekends. Luv the pics. Hope you and your fam are doing well. Cheers!
At 10:10am on March 30, 2011, Doris D said…
At 8:00am on March 30, 2011, Marie B said…
hi Natasha, Happy Birthday and greetings to Sam too!
At 4:43am on March 30, 2011, lotsofshots said…
Hi there, I hope that you have a super fantastic Happy Birthday today!
At 7:20pm on March 11, 2011, Schmutz said…
Those smiles are Infectious!!!!
At 7:40pm on January 19, 2011, Leah D. Rogers said…
Hi Natasha, Wow...where does the time go? Your family pics are great! About the Dex...I love it but we found out that Jillian had been "telling" us her numbers during the day based on the Dexcom and not her meter. There were a couple of days that she hadn't used her meter nearly the entire day....she was basing everything off of the dexcom. So we have given it a break for the past week (she doesn't like the two sites and the extra "thing" that she has to carry around). Have you had any issues with your son not testing with his meter because he has the dexcom? Take care and I look forward to hearing from you :) Leah
At 2:08pm on January 14, 2011, Marie B said…
hi Natasha, thanks for adding me! I see Sam is a Redskins fan. Since I grew up in Alexandria Virginia, we were big fans too. Now I live in rural NW New Jersey. You and your kids have beautiful smiles!
At 11:29am on April 9, 2010, Roxanne said…
Hi. We are changing his sites every 48 hours. We are now using the contact Detach infusion sets. They are working so much better! We have seen an improvement in his blood sugars. Dylan and I are both on the Animas Ping.
At 1:23pm on March 26, 2010, Roxanne said…
Hi Natasha. My son is 4 and was diagnosed in August 2009. Did you go to Childrens in DC when diagnosed? How did you get such a nice A1C? We just started on the pump in February and we are still struggling. Any advice?
 
 
 

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