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Friday
Jul032009

Great Customer Service

Insulet, the company that makes Arden’s insulin pump is sending a nurse to Arden’s new school later this summer to train the school nurses and Arden’s teachers on the OmniPod... free of charge!  

 

We already couldn’t be more happy with our choice of insulin pumps and it seems like every time we turn around the up side of the OmniPod just gets better.  I’ll begin blogging very soon about what we are doing to prepare Arden for kindergarten.  Keep and eye out for that in Daddy’s Blog in the coming days.

 

**

The following are archived comments from this post. You can post new comments below.

Emily
Hey, yeah, Arden IS starting kindergarten soon--she's growing up really fast.  Is she more excited about starting school, or nervous?
Monday, August 24, 2009 - 11:07 PM

 

Friday
Jul032009

Keep Rubbing

Type I has a habit off effecting your life in ways that you could never dream of.  If you know us you’ve undoubtably thought on at least a few occasions, “Kelly and Scott look tired” and one of the reason that you’ve thought that is Arden’s leg pain. 

 

Often after a day of activity or a day that controlling her BG was difficult her legs will begin to ache terribly in the evening and they don’t stop aching all night long.  The only thing that makes her feel better is when Kelly rubs her legs.  The trouble is that when the rubbing stops the pain returns almost immediately.  We can’t share the rubbing duty because Arden only wants her Mom to do it so Kelly stays awake most of the night trying to assuage Arden’s pain.  At this point I couldn’t tell you how many sleepless nights that Kelly has logged rubbing Arden’s legs but if I were to guess I’d say it’s easily thirty, probably more and there is definitely more to come.  

 

It doesn’t seem to matter how well she stays hydrated during the day... if the pain is coming, it’s just coming.  I’ve watched Kelly begin rubbing at 8 p.m. and only be able to stop for short stretches once in a while.  When Kel is able to get Arden to fall to sleep, the sleep doesn’t last long, inevitably the pain wakes Arden and the process starts over.  The stress that accompanies all of this is compounded by Arden’s pleas for Kelly to help her.  

 

It seems that many kids like Arden get this ‘type I ‘side effect’.  The leg cramping is apparently pretty common amongst kids with type I diabetes.

 

You’ve heard me say before that type I is a 24/7 disease, it doesn’t care what day it is, what your plans are or if you’re parents are exhausted, it just keeps coming.  This is the part where I ask you to please keep the Juvenile Diabetes Research Foundation in mind the next time you want to make a charitable donation.  Please donate as generously as you can.

Type I has a habit off effecting your life in ways that you could never dream of.  If you know us you’ve undoubtably thought on at least a few occasions, “Kelly and Scott look tired” and one of the reason that you’ve thought that is Arden’s leg pain. 

 

Often after a day of activity or a day that controlling her BG was difficult her legs will begin to ache terribly in the evening and they don’t stop aching all night long.  The only thing that makes her feel better is when Kelly rubs her legs.  The trouble is that when the rubbing stops the pain returns almost immediately.  We can’t share the rubbing duty because Arden only wants her Mom to do it so Kelly stays awake most of the night trying to assuage Arden’s pain.  At this point I couldn’t tell you how many sleepless nights that Kelly has logged rubbing Arden’s legs but if I were to guess I’d say it’s easily thirty, probably more and there is definitely more to come.  

 

It doesn’t seem to matter how well she stays hydrated during the day... if the pain is coming, it’s just coming.  I’ve watched Kelly begin rubbing at 8 p.m. and only be able to stop for short stretches once in a while.  When Kel is able to get Arden to fall to sleep, the sleep doesn’t last long, inevitably the pain wakes Arden and the process starts over.  The stress that accompanies all of this is compounded by Arden’s pleas for Kelly to help her.  

 

It seems that many kids like Arden get this ‘type I ‘side effect’.  The leg cramping is apparently pretty common amongst kids with type I diabetes.

 

You’ve heard me say before that type I is a 24/7 disease, it doesn’t care what day it is, what your plans are or if you’re parents are exhausted, it just keeps coming.  This is the part where I ask you to please keep the Juvenile Diabetes Research Foundation in mind the next time you want to make a charitable donation.  Please donate as generously as you can.

Type I has a habit off effecting your life in ways that you could never dream of.  If you know us you’ve undoubtably thought on at least a few occasions, “Kelly and Scott look tired” and one of the reason that you’ve thought that is Arden’s leg pain. 

 

Often after a day of activity or a day that controlling her BG was difficult her legs will begin to ache terribly in the evening and they don’t stop aching all night long.  The only thing that makes her feel better is when Kelly rubs her legs.  The trouble is that when the rubbing stops the pain returns almost immediately.  We can’t share the rubbing duty because Arden only wants her Mom to do it so Kelly stays awake most of the night trying to assuage Arden’s pain.  At this point I couldn’t tell you how many sleepless nights that Kelly has logged rubbing Arden’s legs but if I were to guess I’d say it’s easily thirty, probably more and there is definitely more to come.  

 

It doesn’t seem to matter how well she stays hydrated during the day... if the pain is coming, it’s just coming.  I’ve watched Kelly begin rubbing at 8 p.m. and only be able to stop for short stretches once in a while.  When Kel is able to get Arden to fall to sleep, the sleep doesn’t last long, inevitably the pain wakes Arden and the process starts over.  The stress that accompanies all of this is compounded by Arden’s pleas for Kelly to help her.  

 

It seems that many kids like Arden get this ‘type I ‘side effect’.  The leg cramping is apparently pretty common amongst kids with type I diabetes.

 

You’ve heard me say before that type I is a 24/7 disease, it doesn’t care what day it is, what your plans are or if you’re parents are exhausted, it just keeps coming.  This is the part where I ask you to please keep the Juvenile Diabetes Research Foundation in mind the next time you want to make a charitable donation.  Please donate as generously as you can.

Wednesday
Jun242009

JDRF's Children's Congress 2009

WASHINGTON, D.C., June 22, 2009 -- More than 150 children and teenagers throughout the U.S. with type 1 diabetes are in Washington, D.C. this week to advocate for funding for type 1 diabetes research.  They'll be joined by JDRF International Chairman Mary Tyler Moore, Nick Jonas of the Grammy nominated multi platinum group The Jonas Brothers, boxing legend Sugar Ray Leonard, and other advocates at the sixth Children's Congress of the Juvenile Diabetes Research Foundation.

 

 Children's Congress, the largest grassroots advocacy event held in support of research for type 1 diabetes, will include a visit with President Barack Obama at the White House, a Town Hall panel of athletes and celebrities impacted by diabetes, and a hearing on Wednesday before the Senate Committee on Homeland Security and Governmental Affairs to request federal funding for diabetes research and remind Congress about the urgent need for a cure for the disease.

 

The Senate hearing, "Type 1 Diabetes Research: Real Progress and Real Hope for a Cure," will include testimony from Ms. Moore, Mr. Jonas, Mr. Leonard, Dr. Griffin Rodgers, Director of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), and four children with type 1 diabetes. The hearing will be chaired by Senator Susan Collins (R-ME).   Following the Senate testimony, the delegates and their families will visit individually with their respective Members of Congress to educate for a cure.

 

A Town Hall panel, "Role Models in Diabetes," on Tuesday will enable delegates to interact with athletes, musicians and doctors who also live with type 1 diabetes - and share their experiences on how they're managing the disease and fulfilling professional careers at the same time.  Panelists will include professional concert cellist Alisa Weilerstein; Miss Black USA 2007 Kalilah Allen-Harris, NFL player Jared Allen and Dr. Aaron Kowalski, JDRF's Research Director for the Artificial Pancreas Project.  ESPN broadcaster Brian Kenny will moderate the forum.

 

 The 150 children- ranging in age from 4 to 17 years old represent each state.  Joining the children in Washington, D.C. are five International Delegates from Australia, Canada, Denmark, Israel, and the United Kingdom.

"The day that you or your child is diagnosed with type 1 diabetes is a day you will never forget," said Ms. Moore, who has had type 1 diabetes for almost 40 years. "Members of Congress will now have the chance to give these children and their parents another day they will never forget. Instead, this time will be a day of hope instead of a day of fear".

 

The Senate Co-Chairs of Children's Congress 2009 are Sen. Collins  and Sen. Lincoln, and the House Co-Chairs are Rep. Diana DeGette (D-CO) and Rep. Mike Castle (R-DE).

 

Cynthia Ford, of Grosse Pointe Farms, Michigan is Chair of Children's Congress 2009.  Ms. Ford, her husband Edsel and son Albert, who has type 1 diabetes, serve as the designated Chair Family.

 

"Our entire family understands what a vital role this event plays in the furthering of our mission to cure diabetes. We are honored and excited to be leading such an extraordinary group of delegates who truly will have all the Washington leaders knowing they need to 'Promise to Remember' all of us who crave a true cure for diabetes and its complications."

 

Children's Congress, held every other year since 1999, has become the largest media and grassroots advocacy event held in support of finding a cure for type 1 diabetes. A once-in-a-lifetime experience, the delegates help raise awareness about type 1 diabetes, and participating in personal advocacy at the highest level of U.S. government.   

 

In type 1 diabetes - the most serious and complicated form of the disease that accounts for at least $174 billion in annual health care costs in the U.S. alone - a person's pancreas stops producing insulin, the hormone that enables people to get energy from food.  To survive, people with type 1 diabetes must test their blood sugar levels up to four or more times a day by pricking their fingers to draw  blood, and then administer  insulin through multiple daily injections, or the use of a continuous infusion insulin pump. 

 

While trying to balance insulin with the amount of food eaten (which raises blood sugar) and exercise (which lowers blood sugar), people with type 1 diabetes must constantly be prepared for potential life-threatening low or high blood sugar levels.  Just as devastating, the long-term complications of diabetes include blindness, heart attack, kidney failure, stroke, nerve damage and amputations.  While usually diagnosed in childhood, type 1 diabetes can also be diagnosed in adults.

 

http://www.jdrf.org/index.cfm?fuseaction=home.viewPage&page_id=0DC7B049-1279-D3DC-F950837CA88D7C92

Tuesday
Jun022009

JDRF Promise Meetings

As part of their effort to educate our Senators and Congressmen about type I diabetes the JDRF schedules group meetings between the people effected by type I and their local legislators.  You may remember that Arden and I attended one last year with our Senator.  So if you are the parent of a child with type I please consider attending a meeting and sharing your story.  Who knows... you may be the reason that the Special Diabetes Program doesn’t experience a cut in federal funding.  


From the JDRF: Because you or someone you know lives with type 1 diabetes everyday, you know that we need a cure.  JDRF’s top priority is securing the necessary research funding to discover a cure for type 1. Along our path toward a cure there will also be milestones achieved that will make it easier for people with type 1 to manage the disease, reduce complications, and enjoy a better quality of life.

 

The 2009-2010 Promise to Remember Me Campaign will be focused on both of these priorities. JDRF advocates will be scheduling meetings with their Members of Congress to:

 

• Ask them to co-sponsor legislation to, once again, extend the Special Diabetes Program and avoid a 35% reduction in federal funding for type 1 research; and

  1.  Make sure that the needs of those with diabetes are included in legislation to reform America’s healthcare system, including providing access to quality and affordable coverage without exclusions or penalties for pre-existing conditions.

 

The goal of the Promise Campaign is to communicate this message through personal meetings with Members of Congress when they’re at home. 

 

Signing up to attend a Promise Meeting only takes a moment and you can do it at this link.

Tuesday
May262009

OmniPod v Pool

Arden swam everyday this weekend, she spent hours and hours in the pool -- all while wearing her OmniPod.  Because of that she never had to be disconnected from her insulin supply which made it much easier for us to regulate her BG.  The OmniPod really is an amazing device!!!