Road ID. I wear one daily for my safety with Type 1 Diabetes.

Monday, May 16, 2016

Pump sites and healing them faster

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Recently in a support group I am in the topic of insulin pump sites and healing came up.  A few ideas were shared and I just wanted to share what I use, for a non-medicated approach.

After my friend told me about Bio Oil and finally trying it, I was sold. I really like it, it absorbs quickly with no oily residue. For me it helps heal my site faster with less scaring. As far as scaring goes, I know all about it. Everything leaves a scar on my skin, including every single pump site. I have a map on my skin of previous sites. The bio oil helps them heal much faster and the scars fade quicker.

I also use shea butter. I just use the Keri brand mostly but Bath and Body Works has or had great scents in their body butter lines which has shea butter in it. The keri brand is a bit greasy so I only wear it at night but the Bath and Body Works one could be worn anytime for me anyway, maybe not hot summer days though. Itll make you sweat and then your slimy. Yuck.

I try not to use steroid creams or antibiotic creams, as long term use of any of those isnt good. Steroid creams will thin your skin and antibiotic creams can give you dermatits and set you up for antibiotic resistant infections.

I hope this helps someone else out there.

Please leave me your comments, it helps keep me motivated!

Diabetes Blog Week - Message Monday


Diabetes Blog Week Day 1 topic: Message Monday:  Lets kick off the week by talking about why we are here, in the diabetes blog space. What is the most important diabetes awareness message to you? Why is that message important for you, and what are you trying to accomplish by sharing it on your blog?

Want to join Blog Week?  Check it out here:

I started my blog in 2013 for the most part, I posted just a few things in 2012, but its not worth talking about.  Most of my Diabetic life I had not known anyone with type 1 Diabetes, other than my 2 brothers and some family members, and wasn't in any support groups and I wasn't comfortable asking the people I knew some of the personal questions I had.  I felt alone and misguided.  Most of my Diabetic Career before I met the medical team I have now was full of bad information and almost no guidance.  After I found my awesome CDE (Calli) and how completely fabulous she was, I felt inspired to help others, as she helped me so much. 

I joined some facebook support groups, saw how many other people we also getting bad medical advice and then I found other Diabetic Bloggers.  I knew and saw how many people were also lost and felt alone in their daily life with Diabetes.  Many people I know in my area or live in my area, I actually insisted that they too go see Calli, because of her great understanding of Diabetes.

Then one day the idea of starting a blog came to my mind and overnight I thought of the name I am a type 1 Diabetic Warrior, differentiating my type because of all the misinformation about Diabetes and the fact that there are two types.

I blog to share my life and trials and tribulations with type 1 Diabetes because so many of us out there feel so very alone because it is basically a hidden disease until issues or complications arise. 

There typically isn't much if any support from fellow family members and friends as with any disease that is not visible to the outside world.  You have to seek support from the community of people who are also living with the same disease as you are.  You have to learn how to cope with the general public's misguided comments and information, which can be very hard at times and can hurt quite a lot. 

I also blog to share the low carb lifestyle I decided to begin in April 2015.  It has changed my life and the ease of managing my disease and how much healthier I feel.  It is also a very hard pill for most people in your life to swallow and you get a lot of push back, which in turns makes it even harder to stay on track.  It can be done, it just takes more time and being on the receiving end of more insensitive comments.  The longer I stay on the low carb track, sharing really good recipes and people saying how much they like the food keeps me motivated and I have actually helped to inspire a few people I know to try low carb or do more low carb food, which makes me so incredibly happy. 

All I want to do is help people live with Diabetes and live as healthy as they can.  It brings me great joy to have someone come up to me and tell me they tried this or that recipe or they went to see Calli or Teresa and they loved her and/or they decided to go on an insulin pump or CGM.  It makes my heart so happy to know I helped put them in the right direction.  So to all you who have told me I helped you, I am forever grateful that I could help you, just by being another person with Diabetes and sharing my story and my experiences over and over and over again.

Please leave me your comments, it helps keep me motivated!

Medicare Told to Cover CGMs in Ruling

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Medicare Told to Cover CGMs in Ruling

 This could be a huge decision for Medicare coverage of CGM technology. We NEED Medicare to cover CGM's for people with Diabetes!

Please leave me your comments, it helps keep me motivated!

Tuesday, May 10, 2016

diaTribe's reaction to the UHC/Medtronic pump deal

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 #MyPumpMyChoice #accessmatters

diaTribe also released their reaction/letter about the UHC Medtronic deal.

Please leave me your comments, it helps keep me motivated!

American Diabetes Association reaction to UHC/Medtronic deal

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#MyPumpMyChoice #accessmatters @myUHC

Keep them coming Diabetes Community!  We have got to get UHC to change their mind and not take this one track approach to such complex complicated Diabetes management tools like Insulin Pumps!

Please leave me your comments, it helps keep me motivated!

Friday, May 6, 2016

JDRF release letter about the UHC/Medtronic agreement

1 comment:
 #MyPumpMyChoice, #AccessMatters

 JDRF came out with a letter about the United Health Care / Medtronic deal that was announced this week and as it should caused a big uproar in the the Diabetes Community.

We need access to all the pumps available to use the one that fits us best and to keep insulin pump competition and innovation alive.  You kill off all your competition by negotiating contracts with huge health insurance companies and then they have no reason to be on the cutting edge of innovation. 

For example in the CGM field.  There use to only be Medtronic CGM's and they were terrible, almost every single person who wore one hated it and a lot of people still hate the new Enlite sensors.  Then Dexcom came along and knocked all our socks off, it is a much better sensor.  It is so much better than most of the research going on in the closed loop artificial pancreas projects USE a Dexcom CGM.  So what happens when you cut out pump competition, you force out innovation and competition to come out with better pumps!
Please leave me your comments, it helps keep me motivated!