Thursday, October 20, 2011

A New Adventure Coming Soon

Hi to everyone I know I never blog very much at all, and to be honest I feel like I am not a very creative writer and frankly blogging takes more time than writing a quick status on facebook. So here I am about to tell you all that has been going on since my last blog a month ago.

After careful decision making for almost two months of reading and asking questions to all my other D families we have decided to start pumping and have chosen the OmniPod. Sweet and Sassy has always said " I do not want anything attached to my waist all day long." and with that being said we never pushed the issue. That all changed when we found out about the pods. Since Sept 17 we have been in the process of getting all this started. As of Monday this week we have our Omnipod now just waiting on a call from the Dr's office to get it connected. I am excited and a nervous wreck about starting this adventure. I know there will be many bumps along the way just like when we were diagnosed.

I really am going to try and post more on here...I know I know I keep saying this but I really want to post more I do. If we could only have more time in the day to get things done. Hope all my D families are doing well.

Sunday, September 18, 2011

HUGE SUCESS

So back in August I had an idea to do a fundraiser to raise money for JDRF.After about a day of thinking I decided to do one with bowling. Where kids can be involved too so it was just not for adults since these was my daughter. I decided to call it Strikes for Sweet and Sassy's Diabetic Courage. I was very apprehensive about this. Would it be a success? Would we make money? Who would actually show up. With all of this going through my head I thought why not if it does not go well who cares we had fun. Boy was I wrong after I posted it on Facebook we had a huge response but then again I found myself questioning myself the closer it go to September 16. I had put alot work, time and money into this. We had 50/50 tickets and 5 raffles items.

As the days followed I prepared pictures and a video. I am not a crafty person in anyway shape or form. I had no clue had to make a video but I figured it all out.

So the night was here I was so afraid that everyone who said they were coming would call and say "something came up we wont make" thinking in my head what I would say back to them. What i want to say is "What if this was your son/daughter that went through living with Type 1 everyday?"

All the worrying for nothing this event was a huge success with family and friends and will defiantly be a event we will do everyday. The evening went by so fast I was busy talking and thanking everyone for coming I barley had time to enjoy any bowling with my daughter. She had a blast along with everyone else who was there as well.

In the end after paying for all the bowling, pizza and soda we raised $471.00 to take with us on our walk October 9.

I am truly from the bottom of my heart so thankful for all our family and friends that came out September 16 to make this event a success they will never know much this meant to me.


Her two older brother Chase (left) Damian (right)

Friday, September 9, 2011


Cadence wearing her sample Omnipod

A little bit of everything

When I started blogging back in July I thought I would blog something every day...boy was I wrong. Since I started this life has been a whirlwind of ups and downs. It started out with my friend loosing her 21 year old son, then Blake's grandpa passed. I decided to go back to work applied for several jobs on Monday August 7 got a call that day for an interview the next morning that afternoon they called and ask if I could the next day. So I had to find a sitter for Sweet and Sassy that I could trust and know how to take of her. I was pretty lucky I had a few in mind that I was given names of . The first person I called was the one. Her daughter has Celiacs Disease so she was very understanding that of reading labels and measuring food out. Thank goodness she was able to take her at the last minute.

Then we had our 3 month endo appt it went great...we are now going to start pumping with Omnipod super excited about this change. Sweet and Sassy wore a sample Omnipod prior to our appt. We go Sept 17 for our pump class then go from there. Lots of good things I hear about the Omnipod.

Then school started...all went well no complaints here. The nurse is wonderful with her. I never feel like she is not taken care of. The nurse will text me all her numbers througout the day or if she has any questions about anything! LOVE LOVE LOVE

Then over Labor Day weekend I took my 1st trip without Sweet and Sassy since she was diagnosed. Blake and I went to Florida to pack up his granparents place and drive their car back. The getaway was great but I worried the whole time I was gone. Thanks to Misty over at Life Is Like a Box of Chocolate's for being on call all weekend if needed. My mom did have to call her just for reassurance. Sweet and Sassy then went to stay with her dad on Friday evening let me just say this was not what I expected.
Her dad just dont get it sometimes he gave her donuts every morning for breakfast and pizza every evening for dinner....WHAT WAS HE THINKING!!!!! Do not get me wrong I do let her have those types of food but not everyday.

Well with all this I am going to try harder to at least blog once a week from now on...we will see how this goes. I truly love doing this and reading others blogs well. Hope everyone has a great weekend.

Michele

Wednesday, August 17, 2011

Busy.........

Life as been hectic the last few weeks...and sure does not look like it is going to slow down anytime soon. With the first day of school sneaking up on us we have our endo appointment in the morning. Hoping and praying a good visit as well as to some answers. Sweet and Sassy has been running extreamly high at night with ketones and nothing we do seems to be working to our advantage. By morning she is back to normal so who knows with disease somedays.

She has been wearing a sample of the OmniPod in hopes of this is what we will get in the next couple of months, she seems pretty excited about it.

Hope everyone is enjoying your last few days with kids before school is back in session and that we all have our 504's ready to go.

Will try and report back tomorrow about our visit.

Thursday, August 4, 2011

Crazy

The last week has been a nightmare any parent should never have to go through. My friends son did not make it he passed last Saturday. He physcially was doing ok but on Friday they did brain function test and he was brain dead. VERY SAD! The family is holding up way better than I would be. As I writting this i just a got text from her that said " We ordered a beautiful headstone!! Thanks for being there and you can"t live your life in fear of Cadence's disease. Just enjoy her don't fear the disease god wouldn't want you to be so stressed living day to day scared it's out of control as I found out." My heart aches for her.

Since this has happened to her, I am now more than ever worry more about BG. I know we have them under control and she is doing good, but us T1 mamma's know this could change in a blink of eye.

Well just wanted to give an update with her son since i posted last week about him. Thanks to all your prayers keep them coming they will need them in the next upcoming weeks and months.

Wednesday, July 27, 2011

STRESSED

First of all I want to thank anyone who has commented over the past few days its been very stressful around here as you are about to here!

Sweet and Sassy's BG have been extreamly high at night in the 300's and low 400's but has been great during the day, no high's or low's. I think we have it under control now. I have been increasing her Lantus as of last night it's working, let us hope tonight is good too. I need some sleep more than 2 hrs at a time!

Then our air is out. Been having companies in out getting estimates. We think we have one now should be installed next week sometime. It has not been to hot as our's still works some what.

Blake's grandpa is not doing well at all. He is now in Hospice care only drinking not eating. They are saying its a matter of days. He is Florida. I keep telling Blake to go see him I do not want him to miss out on saying good-bye and then regret it later. I know we have alot going on here but I can handle it. So not sure how to handle him not wanting to go. I am thinking it is just a guy thing.

My friend Jeannette found her 21 yr old son unresponsive she had to give him CPR. He has blood clots they think with all the CPR the clot broke up and moved to his lungs which was lying on his heart. He has flat lined three times since Monday I was told. He is on a hypothermia machine to help with the brain function. He is 65% vent and 35% of his own breathing. He truly needs a MIRACLE! He had told his mom about a month ago he thought something seriously was wrong with him. He just graduated college and was engaged. The family had also taken a trip out west about a month ago as well.

I feel so HELPLESS to all the ones around me right now. Knowing there is nothing I can say or do to make things better for any of them. All I can do is be there when they need me.

I know alot of this had nothing to do with her BG's but please keep them all in your prayers.

As a mother I can not even imagine what she is going throguh. I hope and pray I never have to either. If none of this makes any sense it is beacause I have had a waterfall on the whole time I have been typing.

Michele