TuDiabetes - A Community for People Touched by Diabetes

Penny R.

Penny R.'s Blog (15)

Why I hardly ever post here

Hi guys. I hardly ever post here. But, I'm around. I visit often and join in discussions occasionally.

I just wanted to refer you to my regular blog. I've been posting at My Son Has Diabetes for a little over 2 years now. That's why I never post here. It's hard for me to keep up with one blog, let alone two.

I probably won't post here again. I have a feed to my blog on my tudiabetes page so my most recent post is always in the

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Added by Penny R. on February 1, 2008 at 7:39am — 1 Comment

Check out my video

Please take time to go to the video section and check out my video entitled Walk of Hope 2007.

It is the video I made for my walk this year.

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Added by Penny R. on November 20, 2007 at 6:40am — No Comments

A Strange Question

I was speaking to another mother of a child with D today about Walk of Hope. I had invited her daughter to come out and walk as well as to be included in my Faces of Hope presentation. I didn't even ask for a donation because I knew they participated in a JDRF walk.

She said she had never heard of The Iacocca Foundation. I wasn't surprised. I'm sure plenty

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Added by Penny R. on October 3, 2007 at 11:10am — 3 Comments

Does this bother you?

I'm paraphrasing here, but read this statement from a radio ad and see what you think:

"...kids eating school lunches leading them down the path to obesity and diabetes"



Does that statement bother anyone else?



It is a radio ad for Boar's Head turkey. I'm in the car a lot and I hear this ad everContinue

Added by Penny R. on September 21, 2007 at 6:09am — No Comments

Hopeful Faces

Walk of Hope is coming up in a few short weeks. I am doing a presentation again this year entitled "The Faces of Hope".

It's just a little slide show of people with Type 1 with a info like their age, age at diagnosis, hobbies, where they live (if they chose to share). Along with that I need a picture.

I had 22 hopeful faces last year. But, this year I only have 10.

If any of you would like to help me out I'd appreciate it

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Added by Penny R. on September 19, 2007 at 1:53pm — No Comments

Choking Back Tears

About three weeks after Riley was diagnosed, he checked his own sugar for the first time. But, then, we started checking it for him. It was just easier (and quicker) that way.

Michael and I have been talking lately about how we need to start getting him back in the habit of checking his sugar himself since he will be checking it once he starts school. But, I’ve been putting it off. I didn’t really know why. I thought maybe it was because it’s just easier to do it myself.

Michael

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Added by Penny R. on September 19, 2007 at 6:20am — 3 Comments

Freaking lows

Riley's had quite a few lows lately. I'm talking 40s and 50s. They started on Friday. We went to a football game and he played in the playground the whole time (with a decreased basal), he started running low after that, but I thought I just didn't decrease his basal enough.

I've increased his insulin sensitivity factor. I've decreased his basals and yet he's still going low. I'm even subtracting insul

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Added by Penny R. on August 29, 2007 at 1:50pm — 1 Comment

Sometimes it soars

In the past I've struggled with my belief that there will ever be a cure for Type 1 diabetes. I finally decided that I would hope for a cure but not really expect one.

Today I opened my email and found
this. It's an update to the Denise Faustman trials. They are moving forward ahead of schedule. She has cured mice. And, I'm hoping she can cure my son.

Most of the time m
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Added by Penny R. on August 4, 2007 at 12:41pm — 3 Comments

Walk of Hope

I just wanted to mention my walk here. I don't need to give you guys the statistics. I don't need to review how often Riley gets stuck with needles or how he feels when he's high or low. I don't need to spout of the statistics of shorter life spans and complications. You know all that already. You live it.

You know why we need a cure. Soon. All the advancements in CGMS and newer insulins are great, but I want a cure.

That's why I am sponsoring my own walk. There is not a local w

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Added by Penny R. on August 3, 2007 at 5:50am — 5 Comments

Faces of Hope

At Walk of Hope last year I did a presentation entitled "Faces of Hope".

I had people with type 1 diabetes email me pictures of them or their child along with name, age, age at diagnosis, where they live, basically whatever info they felt comfortable sharing. I had about 20 people send me pictures.

My purpose for doing this was to show those in attendance that this isn't only about my son, but also the millions of others who live with this disease every day and to show that thos

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Added by Penny R. on July 31, 2007 at 6:19am — 1 Comment

Not Today

There are times with this disease when I think things aren’t so bad. Riley is healthy. He’s happy. A lot of the time his sugars obey (for the most part).

He swims. He runs. He laughs. He does all the things a normal 5 year old does.

Yep, sometimes I can fool myself into thinking everything is fine. I look to the future and see the awesome possibilities.

Then, we have a few days of high sugars, ver

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Added by Penny R. on July 19, 2007 at 7:13am — 3 Comments

Proud

I’ve been spending a lot of time on tudiabetes lately reading stories of other parents. The parents of kids with type 1 group now has 45 members. While it’s great that the resource is there, it saddens me that these people fit into this group at all.

Some parents there have been living this disease through their chi

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Added by Penny R. on July 10, 2007 at 11:23am — 1 Comment

Because I Have To

This is a post I wrote on my blog back in January. I thought I'd share it here.

It was 4:30 in the morning. I heard a voice coming from the other room.

“Daddy?”

I nudged Michael to wake him and told him Riley had just called him. He immediately got up and went to see wh

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Added by Penny R. on June 26, 2007 at 1:55pm — 4 Comments

parents of kids with d group

Hi all you parents of kids with Type1!

I just wanted to let you know that I started a tudiabetes group for parents of kids with D if you'd like to join. That will make it easier for all of us to connect with each other.

Take care,

Penny

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Added by Penny R. on June 22, 2007 at 6:06am — No Comments

Introduction

Hi all.

Just wanted to introduce myself a bit. I have 2 beautiful boys and a wonderful husband. My oldest, Holden, is 16. And my youngest, Riley, is 5.

Riley was diagnosed with type 1 diabetes in October '05 when he was 3. He started on an Animas insulin pump in March of '06.

It's taken me a while,but I think I've finally gotten over the initial shock and overwhelming grief that comes from being the parent of a child with D.

I'm not sure how much I'll post here, so

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Added by Penny R. on June 14, 2007 at 10:32am — 2 Comments

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