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Entries in Guest Post (18)

Wednesday
Dec052012

Stop saying "Cure" at Diagnosis

I want to thank the Co-founder and President of Diabetes Daily David Edelmann for inviting me to contribute periodically to his wonderful site. Moreover, I want to thank him for understanding when I expressed my desire to repost on Arden's Day, in it's entirety, my work after it had run on his site. This is not the norm and generous of David to agree to. Reposting is not an attempt to "double-dip", it is being done so that all of my diabetes writing can be housed on Arden's Day for reasons of backup, cataloging and posterity. Please know that I was not paid for writing on Diabetes Daily nor did I compensate them. With that said, here is my first piece for Diabetes Daily as it ran on November 16, 2012.

 

Using the Word "Cure" at Diagnosis... Must Stop!

Before we left the hospital after Arden’s diagnosis the doctor told us that she expected type I to be cured in lab mice within a few years. That breakthrough, she said, would lead researchers to find a way to cure people with type 1 diabetes. 

Every person that I’ve ever met who has type I has a similar story about doctors giving them sincere hope for a cure, and the message they receive is often followed by a time frame: “They’ll cure it in five years” or “Just hang on, a cure is close” or “Ten years, no more.” Why would medical people make you such a promise? Why would they tell us that our daughter had a life-long, incurable struggle, spend days teaching us how to keep her alive, constantly remind us that we are literally learning how to keep her alive, and then drop in the idea that it’s not going to be too long until a cure is found. What would bring a person to say something so cruel? I’ve thought about it a lot and honestly, I think they say it out of compassion. It’s a very short-sighted compassion, but never-the-less….


I personally can’t imagine having a job that required me to tell people each day that something bad, something they don’t deserve is happening to them. I wonder what we looked like when we heard the words, how much anguish did our faces reflect? How could a compassionate person not want to, even in some small way, assuage that anguish.

A few months after Arden was diagnosed I woke up one morning, sat at my computer, and read the world news. I saw the report that brought my spirits to a new high that morning, a level that I had not imagined would ever be mine to enjoy again; someone cured type I diabetes in mice. I cried. Arden was next. This was almost over. Of course it wasn’t, but armed with the words of Arden’s diagnosing doctor, I read this article with no reason not to think a human cure wasn’t mere months away. I mean, it was happening just like she said it would. However, when I began to dig into the research, I found that a few researchers had cured type I diabetes in mice, and that this news was neither new nor a concrete promise that humans were next. It certainly didn’t mean that a cure was imminent.

Since that time I’ve met people who were told “five years”…and that was twenty years ago. In fact, so much time has passed that I am now one of those people. I believe that we should all live with the hope that a cure will be found, but plan and act as if it won’t be. 

I want all of the doctors to know that whatever the reason is that you stand in front of your patients as they struggle to hold themselves up, and promise them something that you have no control or honest idea of; why ever you do that, please stop. When the day comes that they realize that your words were empty, they will feel immeasurably worse then they did and you will have done them more harm then good. You also steal from them the time that they clung to that hope, time that could have been used to really take control of their lives. Diabetes felt like something that we just had to manage until the cure because of what we were told. I would have much preferred to take it with the level of seriousness that it deserves and frankly requires from day one.


A better way to give your patients hope would be to honestly give them hope. Technologies, insulins, community, these are all bright spots that lift Arden’s life. Why didn’t you tell us about them? Why did you release us into a world that was completely foreign and frightening with only a fairy-tale to protect us? You don’t give people enough credit for their strength, you needlessly error on the side of caution when you give us details. Didn’t you see what happened when the Greatest American Hero lost that instruction book? We need all of the details, yes they will be overwhelming, but I promise you not nearly as soul crushing as the day I realized that you were lying to me about a cure. Maybe you didn’t think you were lying, but how in the world could you take that chance, and make that promise? It’s criminal.

I would have liked to have been told that researchers have been trying for decades to cure type I, and their efforts continue, but that I should not hang my hopes on a cure. It would have been nice to receive coping tools, and a complete explanation of the moving parts. An honest and heartfelt message of reassurance would have gone a much longer way then the temporary patch that you put on my grief. It did not hold, it held me back and it gave me one more chance to be sadder then I ever imagined that a person could be.

Please stop saying the word cure just to make people feel better.  

Thursday
Sep202012

Blogging Diabetes Podcast (feat. Me)

Recently Tony Rose interviewed me for his podcast, 'Blogging Diabetes'. We talked about raising a CWD, my new book, 'Life Is Short, Laundry Is Eternal', I got a little mushy about my wife Kelly and much more. I hope you enjoy the episode and if you get the chance, I'd love for you to come back here and let me know how I did.

Direct link to Episode BDP 56

Blogging Diabetes on iTunes

Tuesday
Sep042012

My Guest post at 'The Life of a Diabetic'

Chris at 'The Life of a Diabetic' is running a 'Diabetes Parenting Week' feature on his blog and he was kind enough to ask me to contribute. The piece I wrote titled, 'Letting your Kids be Kids even with Diabetes' kicks off the week today. 

I wasn't just excited to be a part of what Chris is doing becasue he's a good guy and I like his blog, though that was part of my decision making process. Mainly, I love the idea of blogs that are mostly read by PWD hearing a little bit about the CareGiver side of type I diabetes. I hope you enjoy my take on the subject and if you can, please take a moment to let Chris know that you found his site through 'Arden's Day'.

My back to school posts will begin later this week as Arden doesn't go back to school for a few more days.

Talk to you soon, Scott

 

Thursday
Nov172011

Guest Post: Mila Ferrer of Jaime-dulceguerrero.com

I first met Mila Ferrer early last summer while she was investigating different platform options to launch her type I diabetes blog. In only a few months she has proven to be a strong voice in the diabetes blogging community and I am proud to feature her today as my first guest writer. Take it away Mila...

***

Hi, I'm Mila Ferrer, I write a blog in spanish about Type 1 diabetes. Why? My younger son Jaime was diagnosed at the age of three. Since then, our family has been learning and educating ourselves about this condition, to be able to provide Jaime the best care. My blog Jaime-dulceguerrero.com is filled with experiences, education and mostly support to other families. During this learning process we've met the most amazing group of parents and patients, people that are as committed to educate and support as we are. This wonderful community or DOC (Diabetes Online Community) is eager to help, promote education and inform about anything that might be useful to us parents and patients. 

As a parent my first search was to meet other families, having a young kid diagnosed with T1 Diabetes can sometimes be overwhelming, and it's nice to know that we are not alone. Thats how I met Scott and Arden, I started reading his blogs and really connecting with his feelings. My family wasn't alone. Scott and I have decided to share some of our posts, that way we'll keep sharing our thoughts and experiences through this journey.
I want to share with you my thoughts and feelings about the DOC. That group of people who are always there to answer questions and lift your spirit when your feeling blue. This link will take you to the spanish version. I also created a tab on the page that is named Mila's Blog, there you'll find some of my posts translated. Hopefully you'll enjoy my posts and find them helpful to you and your family, feel free to ask me anything in english, I'm fully bilingual (sometimes I like writing better in english than spanish). 
You can find me on Twitter @dulce_guerrero (english and spanish information)
***
Please take a moment to check out Jaime-dulceguerrero.com but before you do... dust off your high school spanish and give Mila's DOC post a read... It is linked above but I'm including it in it's entirty right here.

***

¿Qué es una comunidad? Para mí, una comunidad es un grupo de personas que trabajan o buscan un fin común. Ese grupo de personas que hablan el mismo idioma, viven experiencias similares y se ven reflejados en otras historias. La comunidad se apoya, busca el bienestar de todos y comparte ideas e inquietudes.
Algunos de mis compañeros de viaje en esta travesía llamada Diabetes.

Afortunadamente cuento con una gran comunidad que apoya a mi familia y me ha servido de ejemplo en este gran proyecto de educación.  Me refiero a el DOC (Diabetes Online Community) o la Comunidad de Diabetes en Línea. Esta comunidad cuenta con tanta gente maravillosa, talentosa, inteligente, pero sobretodo comprometidos con la diabetes. Lo más curioso es que no he conocido personalmente a ninguno de ellos, sin embargo en nuestras conversaciones en Twitter o Facebook es como si nos conociéramos de toda la vida. Siempre dispuestos a ayudar, a contestar preguntas y apoyarte cuando te sientes frustrado.

En muchas ocasiones cuando tengo alguna duda o me ha pasado algo fuera de lo común relacionado a la condición de Jaime, recurro a mis colegas blogueros de diabetes. Através del DOC he conocido padres y madres de otros niños igual que Jaime y pacientes adultos que llevan años manejando la condición. Quién mejor que ellos para contestar preguntas, aconsejar y dejarnos saber que no estamos solos. Ellos viven lo que yo vivo, tenemos las mismas preocupaciones y queremos lo mismo; el bienestar de los pacientes de diabetes.

Durante este mes de noviembre el DOC ha trabajado mano a mano creando conciencia y apoyando las actividades benéficas que provean un mejor tratamiento a los menos afortunados, la Gran Prueba Azul fue un éxito. Otra actividad que hizo el DOC fue crear un intercambio de tarjetas postales entre familias y pacientes diabéticos. Alrededor de 530 personas participaron de este intercambio, Jaime envió postales a Canadá, Australia, Reino Unido y varios estados de los Estados Unidos. De igual manera él recibió tarjetas de estos niños, la carita de emoción de Jaime al leer cada postal fue de gran valor. Inclusive hasta una nueva amiguita por correspondencia hizo. Esta actividad nos relaciona con otras personas y crea un lazo muy fuerte entre los pacientes.

Me siento muy orgullosa de pertenecer a una comunidad tan activa y deseosa de trabajar. Una comunidad abierta a recibirte, dispuesta a ayudarte y compartir entre si educación, información y sobretodo apoyo. No estamos solos, hay toda una comunidad que con mucho gusto y placer te darán la mano cuando lo necesites.

***

Mila, gracias por compartir tu blog con mis lectores y por su amistad en elDOC. Mejor de mí, Scott (lo siento, pero tuve que usar Google Translate,espero que funcionó!)

Friday
Aug122011

I am a guest blogger at D Mom Blog

 

Today is a BIG day, no not because it’s my Mom’s birthday (Hi Mom, Happy Birthday!), because I’m a guest blogger today on the D-Mom Blog!

 

All this week the D-Mom Blog has been featuring guest post for back-to-school and today my blog is running on the front page. I wrote about how to build a strong and lasting relationship with the people that care for and teach your children during the long school year.

 

Leighann (D-Mom) called it, a “must read” on her FaceBook page and went on to say that, “Scott is a strong voice in the d-blogging community. His posts are always thoughtful and provide great information. He is one of the few D-Dads sharing his story of raising a child with diabetes.” on her blog.

 

Her blog is a favorite in the diabetes blogging community and it was an honor to be asked to write for it. I hope that you can take a moment to visit my post and perhaps leave a comment. Click on the link below to be taken directly to it...

 

http://www.d-mom.com/diabetes-at-school-building-relationships/

 

**

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

As always, a very thoughtful and USEFUL post, Scott. Thank you for gracing the virtual pages of D-Mom Blog today.
Friday, August 12, 2011 - 10:16 AM