"Hi, I'm Kate. My son who is 6 was diagnosed in July of 2012. He started on the Animas Ping Insulin pump in October of 2013 we had a lot of issues with it. If you want to know the specifics read my blog post about it. So we took him off the pump…"
Thanks for the comment. I don't know why my post did not appear. I had fully intended to take it but fell asleep before I got up to do so! I feel strange about taking it tonight because tomorrow I work..Taking it last night and then having today (Sunday) free to feel for any effects would have been nice. Don't wanna go low at work. Oh well. Gotta get on the horse sometime. I have so many questions because he added two medications and I am concerned about taking them all together, three of which combined may cause low sugar. I have so many questions but he is only here in town on Fridays. Arrgh it is so confusing and scary!
Last Thur. my fam doc's office called, told me to head to ER for an emergency evaluation, as my kidney labs that morning were off. (BG was in the 90s and a1c was 5.8).
After being held captive, stabbed for IV and hooked up to monitors, banded like a pigeon etc etc I was eventually released (they were planning on my spending the night). I do NOT like spending nights in a horsepital, they usually do a bad or worse job of D-management, plus how can on get a good rest in them their horsepitals?
I see my fam doc first thing Monday morning (a couple weeks early,
The person I saw with MS (but not diabetes) was already using a power wheelchair (but still working) when I first met him. He had a van he could drive the power wheelchair into, so that he could drive to work.
Hey! How are you doing? It's been a while since I've been on here. How did your dr appt. go? I got way more than I bargained for when I was at the dr. last time. In fact, I'm still dealing with it.
I think having both MS and diabetes is really hard. There's a lot to deal with and it's different for everyone. I hope we can support each other through all of the good and bad.
Strange as it may sound, I am excited about being sent to the MSU MS (multiple sclarosis) clinic and expect to find out when I go Monday. IF the MS Dx is confermed and become formal, then I may be able to get treatment. I just hope is RRMS and not SPMS. This may also explain so much about my diabetes being wierd as well.
There is a linkage between autoimmune T-1 and MS and I started a new group here for diabetics with MS.
For what seems forever everything got blamed on my diabetes, that is till I saw a new eye doc who explained WHY my diplopia was NOT diabetes related. I have had diplopia since I was 18. one thing led to another etc etc etc so maybe just maybe I will learn WHY I became a GOMER and instead of going down hill may be able to level things off a bit, or even improve things like my mobility.
See I was a little worried because sometimes I see a little bit of lingering bubbles ... but they never last more than well i'd say 30 seconds to a minute tops....my doctor did blood work and multiple strip tests and said because the bloodwork was so excellent he and the tests at all times of day have came back negative he was not concerned..maybe just the meat I had eaten before or glucose in the urine making it appear that way..
I read in a comment on another post about foamy urine...I've always been curious about this as a lot of people get normal urination characteristics....bubbles caused by forceful flow..as opposed to foam which I would imagine looks something like dish soap?
So I guess the question is what does "Foam" due to protienuria look like?
Last month, I had one of the most amazing experiences I have had with technology since I have been living with diabetes. It happened at the Focus On Technology conference organized by Children With Diabetes in Los Angeles (the first Read on! →
REALM Charter is a middle school full of amazing young people eager to learn about World Diabetes Day. Team DHF spent the day with over 300 students and taught them about the Big Blue Test and what they can do Read on! →