Archive for Diabetes champions

All quiet on the Western Front

Hi all!

It’s hard to believe we’re in December, counting down the days until Christmas. We’ve all been running around madly, and I thought I’d just reassure everyone that this blog is quiet, but not forgotten!

Lance has had his 8th Birthday, and he’s been inundated with gifts and love. We expect he will emerge from his own Lego-land sometime in 2012. He wants to thank everyone who has been keeping him in their thoughts and prayers, especially since the diagnosis of peripheral neuropathy. Doctors and health-care specialists are looking into a range of ways of helping him, and Kate is doing everything in her power.

Talking of Kate, she’s just embarked on a new endeavour, and it’s keeping her mighty busy. Which is why I’m writing. Between her job and Lance, she hardly has 5 minutes to herself.

Not a great deal has been happening in the diabetes world, but great news for those in Africa, announced yesterday: Novo Nordisk is providing FREE insulin to 10,000 diabetes-affected children (Danish firm to give African children free insulin – Reuters).

I know you are all keeping both Lance and Kate in your thoughts, and they both appreciate it. Feel free to contact either of them on the email addresses hidden somewhere off on the side-bar there –>

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World Diabetes Day, 2008

More guest posting by Janek!

Once again, World Diabetes Day has come (and gone, sorry for late posting), and it’s been celebrated around the world in many different ways. The theme this year was Diabetes in Children and Adolescents, making it particularly pertinent to this blog. As my darling nephew struggles with his own condition, it’s something that I always think about; or, as Helen Lovejoy cries out in The Simpsons, “Won’t somebody PLEASE think of the children?”. This year, Diabetes Australia worked with the JDRF and hosted a gala dinner (or, as my mother calls them, a galah), as well as hosting a group of sufferers as they climb Mt Kosciouszko.

Girls form a big heart and boys form a big foot to promote good cardiovascular and footcare in diabetics in India

Girls form a big heart and boys form a big foot to promote good cardiovascular and footcare in diabetics in India

I found that part of this year’s campaign was “bringing diabetes to light”, and a number of monuments around the world were lit up in blue. I’ve love to post them all here, but Kate might get annoyed with me, so I’ll direct you to the WDD Slideshow and the Flickr page for the photos, and end this post with my two favourite photos…

San Francisco City Hall

San Francisco City Hall

Nagoya Castle, Japan

Nagoya Castle, Japan

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Wheels Of Fortune.

It’s only just over three months away until the 6th annual  JDRF “Ride For A Cure” takes place.

The Hugely Successful "RIDE TO CURE DIABETES."

The Hugely Successful Ride For A Cure.

My good friend and fellow JDRF advocate/parent, Cathy Forbes and her amazing quadruplet of cyclists are hitting the roads for their third trek through the picturesque Barossa Valley In South Australia.

Cathy, her family and friends have one very special reason why the “Ride” is so incredibly important.

Cathy’s gorgeous daughter, Carrie has the double whammy-Type 1 Diabetes and Coeliac Disease.

The Forbes Family have made an incredible contribution over the years through fundraising, in fact this is their third year that they have rode their way that mile further to finding a cure.

Michael On The Road

Michael On The Road

In January, 2009, Carrie Forbes will have two very important family members, joined by two newbies to the team, who will be riding in her honour. Like any JDRF fundraising event, all donations are put directly into laboratories, research projects and trials, in a desperate attempt to find a cure for type 1 diabetes.

Proud Cathy With Her "Boys."

Proud Cathy With Her "Boys"

On behalf of a JDRF Family who have tirelessly worked and participated in so many fundraising events, I am asking www.whydidtheinsulindie.com readers to think of every child, (or remember when you were one) with this insidious condition. The loose change in your pocket will help to increase Cathy’s fundraising total.

                                                                   

To contribute in any small way to JDRF’s Ride For A Cure 2009, and support my friends, Cathy and Garry, and Lance’s friend (and major crush) Carrie, please click on the below link.

http://ride.jdrf.org.au/CatherineForbes/

  Thanks so much, everyone!

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A Victorious Moment-Paying It Forward To Your Favourite Bloggers!

One thing I have learnt about type 1 diabetes is that just when you think your life is akin to an overgrown bunch of noxious weeds, if you look hard enough, smack bang amidst the jungle you can find the most incredible bunch of exotic blooms.

Today, I found a gorgeous flower that made me smile. In fact, I’m STILL smiling.

My friend Kez sent me an email, and told me that I had a surprise awaiting on his website. After a really horrid day, I was intrigued to investigate.

After scanning through his latest post, I soon found myself grinning, as I had become the proud recipient of the Superior Scribbler Award!

I Won This Award!

I Won This Award!

 

The award was originally created by Melissa over at The Scholastic Scribe. She initially awarded the prize to her five favourite bloggers, who then awarded their five faves, and so on.

My tres amazing hombre, Kez-author of Interpret This! has given me the ultimate privilege of sharing with the blogosphere that Why Did The Insulin Die is one of his favourite blogs! 

Kez writes an eye popping and lusciously addictive blog about everything between his passion for a fine automobile to his quirky, everyday life in Melbourne. Somewhere amongst all of that, you will discover that Kez also has Type 1 Diabetes. I often forget this, however, because he has the ability to just get on with the show. He showers the world with his sunny disposition, and he has a heart as huge as a drag queen’s headpiece. It hasn’t taken long at all for Kez to become someone that I dearly cherish as a friend. He is always looking out for Lance, and he has this amazing ability to make me feel so special. So, Kez, on behalf of the staff of www.whydidtheinsulindie.com (I actually DO have a wonderful team on board, I have my IT guru, my understudy, in case I’m stuck in a crisis or an emergency;he knows Lance and me well enough to take over, and of course, the star of the entire production, Lance,) THANK YOU SO MUCH, Kez, for selecting our little blog as one of your top 5, out of so many worthy and wonderful reads!

So, before I reveal my Top 5 bloggers, I am required to publish the rules of participating in heaping ice buckets full of praise and adoration upon the worthy winners.

 

Each Superior Scribbler must in turn pass The Award on to 5 most-deserving Bloggy Friends.

  • Each Superior Scribbler must link to the author & the name of the blog from whom he/she has received The Award.
  • Each Superior Scribbler must display The Award on his/her blog, and link to this post, which explains The Award.
  • Each Blogger who wins The Superior Scribbler Award must visit this postand add his/her name to the Mr. Linky List. That way, we’ll be able to keep up-to-date on everyone who receives This Prestigious Honor!
  • Each Superior Scribbler must post these rules on his/her blog.

Okay, now that the official part of the post is over, we now get down to the nitty gritty, as i announce the winners, carefully chosen by me, with some very important input from Lance.

In no particular order…

The first winner is Janek, author of The Engineer Also Muses. The name says it all..Janek is an Engineer, working tirelessly (in between msn conversations) to become Dr Janek, by obtaining his PhD. He muses about everything from humourous number plates to posting how many SMS messages he has exchanged with his beloved since they began dating approximately 4 months ago. On a more serious note, Janek is struggling to comprehend with a mysterious burden that affects his home, work and social life. He has an unexplained form of chronic pain, and despite being zapped, prodded and scanned, his medical team are unable to give him an actual reason for why his pain exists, and have therefore lumped his case with the title of nothing short of having a severe case of “Chronic Pain.” Janek manages to keep his head held high and hopes for the best-his wisdom and maturity is so advanced despite his almost 23 years. He is also a passionate advocate for many causes, and when he gets on his soapbox-be warned. Janek is only relatively new to the blogosphere, but has embraced entertaining his readers with gusto. Bravo, Janek.

Kerri‘s award winning blog, Six Until Me, chronicles her last 22 years that she has shared with Type 1 Diabetes. Determined to live life to the fullest, as well as being an amazing advocate for all people with The Big D, her posts leave you with food for thought, empower you to maintain superior health and a positive outlook despite having a pancreas void of insulin, and her ability to share her own terrifying experiences with hypoglycaemia and hyperglycaemia are absolutely heartwrenching. Kerri’s was the very first blog that I came across almost three years ago, I was so intrigued and excited to find an online account of survival that was written by a twenty-something, successful women from Rhode Island who knows her diabetes back to front and inside out. An absolute must read for anyone new to the Diabetes Online Community. I can guarantee that you will find yourself wanting your daily hit of Six Until Me. Oh! By the way, Kerri has managed to make her gorgeous cat an international star! 

Dan, author of My Life In The Slow Lane tells of a young man who has overcome some very dark phases through adolescence with chronic illnesses and depression. He has found the inner strength to live alone in Sydney and attend University, while enjoying an entertaining social life and seducing the reader with his incredible talents as a wordsmith. A inspiring story of how chronic illness could not hold this man back; he managed to emancipate himself from its clutches. Dan can fully identify with how living with Fibromyalgia, ME and Chronic Fatigue Syndrome are so misunderstood, very much like Type 1 Diabetes, often accompanied with the dreaded exclamation, “But you look so well!” A laugh-out-loud account of day-to-day life as a student, a patient, peppered with the excitement and challenges of a flourishing relationship. An inspiring and passionate read, with a twist of ascerbic wit and the odd, unapologetic outburst.

Bitten And Bound The Not So Pretty Side Of Hollywood speaks for itself. An all-girl lineup contribute to this blog (Missy, Meg and Andrea), giving delightfully humourous accounts of C Grade celebrities getting up to mischief.  I  recently enjoyed the Sarah Palin/Tina Fey SNL fiasco that the girls were able to present for our viewing pleasure. Bitten and Bound is your number one stop to find out about scandalous behaviour of the rich and famous, (yes, you, David Duchovny of the XXX Files.) An up-to-the-minute blog about Hollywood behaving badly, with fantastic pics to boot.

And the final spot belongs to..Shannon. This woman is possibly the U.S version of me. Her blog, Mom Wants A Cure tells of Shannon’s eldest child, Brendon, and his diagnosis of type 1 diabetes followed by his survival and the family’s acceptance of The Beast. Unlike me, Shannon has to devote herself to her husband, her two other chlldren and helping Brendon look after his Diabetes, as well as finding the odd ten minutes for herself. Both Lance and Bren were diagnosed at roughly the same time, and are pretty much the same age. Shannon’s blog is a hoot, she is unashamedly honest, (she enjoys colouring her posts with the odd expletive.) I often laugh out loud when I come across expletives used as adjectives or even the only word in a sentence. Dealing with hypos and high blood sugars year after year are bound to bring out some type of frustrated exclamation!) This woman also has the hugest heart and shows so much compassion to those in need of an ear. I relate to Shannon in so many ways, because we both are Mum’s/Mom’s who want nothing more than a cure. “Pure and Simple.” 

 Congratulations to these well-deserving recipients! It was definitely a difficult selection process. Each of these blogs provide me with comfort and much laughter.

Once again, big love and hugs to you, Kez. It was actually very difficult to keep you off my favourite five list!To all of the bloggers who have no reason to include a diabetes info and support blog on their blogroll, but have added us anyway…THANK YOU, TOO!! You are providing an invaluable service, by helping to educate your readers about type 1 diabetes. Better advertising than money can buy, I say! 🙂

 

 

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We Need Your Vote!

Our friend, Cory sent me a fantastic email today. 🙂

 Squidoo, an online organisation that provides phenomenal financial support to charities, are offering a

$80 000 giveaway to many worthy organisations, JDRF INCLUDED!

I am using this post to ask you to help Squidoo, “show us the money!”

You have the power-simply by clicking on Juvenile Diabetes Research FundSquidoo will donate $2 on your behalf!

The most exciting part of the Squidoo Offer, is that JDRF are in the running for an $80 000 donation, if enough people get behind this incredible gesture and VOTE.

Please bare in mind, that the rules do stipulate that you may only vote ONCE-if you do vote more than once, your valuable vote will be deleted.

Do you have a blog? Or a long list of contacts who would love to get involved with helping kids like Lance?

 You can help out AGAIN!

Simply send the Squidoo link to your friends, and ask them to participate! You don’t have to join up or provide any personal details, it’s just a matter of ticking the box marked, “Juvenile Diabetes Research Fund.”

(Technically, JDRF stands for Juvenile Diabetes Research Foundation, not fund, as listed, but hey, when this amazing opportunity is presented, and we score $2 a pop per vote, I’m certainly not going to quibble!)

The closing date for this offer is 15 October-if you can get ten of your friends to vote, you’ve just contributed $20 (thanks Squidoo!!)to the JDRF!

Cory has things covered in America, putting in every effort to make people aware of this fantastic fundraising opportunity. It would be a real honour, on behalf of Lance, and everyone affiliated with  Australia’s JDRF, if you could take a few seconds to “donate” $2, AND increase the overall total. 

It’s an extremely rare opportunity to be offered such a simple way to raise funds for one of our favourite charities who do so much for families and children, living with type 1 diabetes.

PLEASE VOTE!!!

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Austin Cooper: Diabetes Style Guru.

Austin Cooper was fifteen years old when diagnosed with Type 1 Diabetes.

He had to walk away from his old life, and embrace what his new life with Diabetes held in store from him.

After going through booklets and scouring the net, Austin was still not comfortable with the chunky chains he needed to wear for life-saving identification. It doesn’t make a young person diagnosed with this  condition feel any better about it when they are presented with clunky, unhip bracelets with a red cross in the middle screaming, “I’m a walking emergency!!”

In fact, it’s quite poetic.

When I see people with Diabetes dragging the clunky versions of medical ID along with them , it almost feels like they have resigned themselves to the fact that they are “chained” to Diabetes.

Austin tried four different versions of the “chain” before deciding that the market for Medical ID was left behind in a time way before his years. He couldn’t make himself wear what was available, so he decided that he needed to make a difference.

Look no further. Austin Cooper has just brought bling to sting.

Austin’s website, www.evasionid.com, showcases his two very modern, sleek, stylish and funky medical ID designs. They are suitable for anyone with Type 1 Diabetes; on the front,they have a stainless steel engraved medical panel, “Type 1 Diabetes” stamped on the back and are 100% leather to boot!

Not only that, but with every purchase, Austin donates 10% to our favourite charity, JDRF.:D

Take a look at Austin’s Mission Statement on www.evasionid.com.

EvasionID boasts a range of funkalicious, fashionable bracelets that are perfect for day/work/evening wear. They are unisex, stong, durable and very affordable!!  In fact, I announce here on this post, chunky, clunky ID chains-be gone with you!

Whether you are newly diagnosed, a teen, or an adult of any age, Evasion ID has a modern, fresh new approach for your Type 1 Diabetes Medical Identification requirements.

Just in case you missed how much I love Austin Cooper’s new diabetes innovation, check out his website

www.evasionid.com

(My son, Lance already has his picked out. Actually, he wants one in two colours to mix and match.)

While I’m at it, I think huge kudos need to be given to Austin, one so new to life with Diabetes, yet one so determined to honour himself through his creativity, AND the entire Diabetes community worldwide. With 10% of his profits going to JDRF, he is also contributing to help find the cure that kids like my Lance and Austin deserve so, so much.

We, who put fashion before function, we praise you, Austin Cooper!!

 

 

 

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BREAKING NEWS!!! WE ARE OFFICIALLY A NATION OF PUMPERS!

“After demands from parents, the government has agreed to subsidise the cost of insulin pumps for people aged under 18 with type 1 diabetes from November this year, at a cost of $5.5 million over four years.”

Balloons Always Make Me Smile

 

OUR FEDERAL BUDGET RESULTS WERE ANNOUNCED TODAY…..

I CAN’T BELIEVE WE DID IT!!!!

OUR CHILDREN WITH TYPE 1 DIABETES FINALLY HAVE A CHANCE TO LEAD AN INDEPENDENT LIFE, AND ENJOY GOOD HEALTH AGAIN!!!!!

WE COULDN’T AND WOULDN’T HAVE THIS RESULT WITHOUT THE POWERS THAT BE AT JDRF AUSTRALIA.

IF IT WASN’T 4.34am, I’D RING EVERY MOTHER OR FATHER WITH A CHILD WHO HAS DIABETES SO THAT WE CAN CELEBRATE!!!!

YOU BETTER KEEP YOUR WORD, KEVIN RUDD!!!! BUT FOR NOW-THANK GOD YOU ARE OUR PRIME MINISTER!!!!!!!!!!!!!!!!

CONGRATULATIONS, EVERYBODY!!!!!!!!

 

 

WOOOOOOOOOOOOOO HOOOOOOOOOOOOOOOO!!!

 

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The Early Beginnings Of The Juvenile Diabetes Research Foundation. (JDRF)

 

Sometime ago, our library was having a clean-out sale, dumping the “You haven’t been borrowed on a high enough rotation” books, for the gorgeous, paperback variety with the glossy covers that just make you want to glide your hand over its pristine appearance and breathe in the fresh print.

We were handed a large, heavy duty paperbag, the type you would see in an American movie where the checkout chick offers “Paper or Plastic?” Lance and I couldn’t believe our luck-there were literally piles and piles of kids’ books. He was in sheer literary heaven.

A lady with a perfectly placed coiff suggested that I take a browse at some of the parenting books. I told Lance exactly where I would be, whilst his paper bag was quickly growing in size. He gave a hurried nod, and I shuffled over to what looked like a very BORING section.

There were books about how to make your own macrame pot plant hangers, casserole recipe books,” How to grow your own bathroom ferns”, and yes, even a pearler entitled “How to Help your Moggie Have A Home Birth.” I stifled some laughs at the titles that were clearly hot trends circa 1977=year I was born.

Then there were some health books. “How to help your anaemic child..”Growing Pains,or just a Growing Pain?” “Asthma? Is It All About Your Mattress?

The title of the next book wiped the sardonic smirk off my face in a heartbeat.

Parenting A Diabetic Child.

A Practical, Empathetic Guide to Help You and Your Child Live With Type 1 Diabetes.

By Gloria Loring.

 

I stopped, re-reading the title over and over again. Why do I always trip over these rare books, articles, old newspaper clippings.. not that I’m complaining, as they are so pertinent to my life. It’s just that I promised myself a while back, no more diabetes books, they only leave me miserable and swollen with tears that explode five days later at a really inappropriate time…

Anyway,  of course I clutched hold of it, shoved it into Lance’s already bursting bag and paid my $5.

I wanted to go straight home and start power-reading.

It was published in 1991, so I was interested to see if I could source where a particular idea or notion had grown from.  (I could already envisage the many passionate people -myself included-baulking at the title..very unpolitically correct, Gloria!!) But hey, what was political correctness in 1991?

 After reading the book, I wouldn’t have cared if she called it “My Diabetic Kid and Me With My Pretty Little Perfect Pancreas.” She got straight to the heart of the subject and addressed SO many of the issues that an endocrinologist has not and can not give me answers for.

Gloria is actually quite the celebrity, not particularly well known in Australia, (or maybe she is, and not in my circle??) She is the former wife of Alan Thicke,star of 80’s comedy Growing Pains. She has entertained at the Academy Awards, made countless albums, performed with Hollywood’s Greatest and earnt some very favourable reviews. (See below)

She’s been described as having “one of the best vocal instruments in pop music since the salad days of Barbra Streisand.” As a singer/actress/songwriter/author Gloria’s career has spanned three decades encompassing recordings, concert tours, appearances on stage, television, and radio.”

 

She also wrote the theme song for Diff’rent Strokes (that theme song is smokin’!!!!) and Growing Pains…my hero! (I adored these two shows as an 8 year old girl, especially when a television channel put them on back-to-back.

 

All of these accolades are fantastic, but after reading the book, to me, I felt that she was just a parent, like me, with a young boy (Brennan ) who was diagnosed at an early age with Type 1 Diabetes.

Gloria is also an outstanding advocate within the American Diabetes Community. In fact, it was the determination and positivity of her and several other parents that started the JDF-(Juvenile Diabetes Foundation,) which some years later became known as the JDRF;( Juvenile Diabetes Research Foundation.) From a small group of parents who wanted to see their children set free from this condition, it had grown into an annual, million dollar making non-profit Foundation in Australia alone.

Considering Gloria’s book is the best part of 20 years old, she has certainly done her homework. If this was the first book you found and read after your child was diagnosed, you would still have an accurate and rich knowledge base behind you. She writes about all the things that I had always craved answers for, but have had to go through the painful reality of finding them  out for myself, and very often through the cruelest way of all; seeing my baby Lance suffer.

My favourite part of this book is how she states that the then “JDF can only fund only one of out five researchers who wants to do worthwile studies in diabetes. THe U.S. Government funds only one out of four researchers. That means that 75 to 80 percent of the scientists who would like to be working on diabetes-related questions are not able to obtain funding from JDF or the US Government;the two largest sources of diabetes research in the world.”:

She then goes on to say-“A CURE CAN BE FOUND.”

Her reasoning? “During President Franklin Roosevelt’s term in office, a commitment was made to find a cure for polio. It became a priority, and the task was accomplished.”

“The same thing happened after John F. Kennedy inspired us all to believe that we could put a man on the moon. In the same way, with commitment and the proper allocation of resources, we CAN make diabetes a thing of the past.”

When I think of the current Islet Transplant Program that has been in the workings for the past four years, and all of the other scientists that are conducting JDRF funded trials in Australia alone, I suddenly realised that it is reasonable to consider that a cure is possible in Lance’s lifetime.

 Does Prime Minister Rudd not have a major problem on his hands, with 5 children or young adults being diagnosed daily with Type 1 Diabetes, and a shortage of specialists to treat them?

(I am going to send that one particular paragraph from Gloria’s book to Prime Minister Rudd.)

JDRF Australia continiously provide new and exciting developments in the world of Type 1 Diabetes.  They ensure that new and promising research is always continuing, new trials and breakthroughs are always investigated, and desperately needed funds are being raised throughout each year.

However, I think that the unsung hero here is Gloria and her band of parents’ who supported and believed in her sole passion.

 On behalf of Lance and the 140 000 Australians living with Type 1 Diabetes-Thank You Gloria. Parents like you are the people who didn’t flinch when their child was diagnosed, therefore helping other parents have hope, by giving their children belief and self-assurance that one day, they may lead an insulin independent life. We just have to keep hoping,  battling, praying and fighting for this cure. Every mothers’ baby, whether their “baby” is now a fully grown adult or a seven year old boy, deserves to know that there can be miracles if you believe. ( I think I just used a line out of a Mariah Carey/Whitney Houston Duet…) Oh well..it was appropriate, and I don’t think Mariah and Whitney will be too worried.

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May Is JellyBaby Month-Help Us Raise A Million Dollars For The Best Diabetes Research!!

It’s that time of year again!!!

Each May of every year, JDRF Australia and the Type 1 Community celebrates Jelly Baby Month.

The humble Jelly Baby has become quite the unsung hero, even pulling Lance out of a severe early morning hypo at 7am this morning!!! (8 Jellybabies later, and I could gradually see my son returning from the brink of unconsiousness.)

Every year, thousands of JDRF staff, Youth Ambassadors, JDRF Advocates, volunteers and many other generous souls go doorknocking, approach hospitals, businesses, passersby, friends and family, selling packets of Jelly Babies, pens, keyrings, teddybears-all baring the simple but poignant message:

Jelly Babies Save Lives.

Last year, almost $858 000 was raised in the month of May. This year, for the tenth anniversary of Jelly Baby Month, JDRF is aiming for $1 million, that would be donated directly to finding a cure!!!

How can YOU help??? If you shop at any of the 700 Woolworths/Safeways stores within Australia, you will notice at the checkouts colourful boxes, jam packed with the “Jelly Baby” featured everywhere, as well as groovy, fun examples of colourful, exciting merchandise. All products are $10 or less, and anything over $2 is tax deductible.

Amcal Chemists,Medibank Private and Wendy’s also help us out by selling our merchandise.

Who do you contact if you want to make a donation on behalf of a loved one with Type 1 Diabetes???

Juvenile Diabetes Research Foundation — All States (Australia)
Tel 1300 363 126
Email
info@jdrf.org.au

(If you would like to support make a donation exclusively in Lance’s name, please contact our Queensland JDRF Government Programs Manager:)

Queensland – Georgina Duncan on (07) 3221 1400 or gduncan@jdrf.org.au

If every person with Type 1 Diabetes donated $1, we would instantly have over $140 000. ( In 2007, Lance and I raised $2500 on our own, simply by doorknocking from house-to house in our neighbourhood!!!!!)

This is a fantastic project to get involved in. If your children receive pocket money, how about suggesting that they contribute just $2 during JellyBaby Month, explaining that people with Type 1 Diabetes must have numerous needles AND fingerpricks, in order to survive?

Jelly babies save lives – and so can you!

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When Unfortunate Events Happen To People Who Aren’t Lemony Snicket.

 

My friend Jim is the only other person that I know who really understands what Lance goes through with Diabetes. They have very similar issues regarding plummeting hypoglycaemia, and identify with each other amazingly, despite the age difference.

 Jim understands when Lance complains of how a hyper feels.

 Lance understands when Jim complains of a headache that won’t quit post hypo.

 Jim is the only person who truly identifies with Lance’s attempts at describing how having Diabetes feels.

Jim is a man who has survived a lot of heartbreaking blows in his young life. Despite having an extremely rare auto-immune disease, he is able to look at life and laugh and see beauty around him. He is happily married, he has just celebrated his 24th birthday, and has new and exciting ventures coming his way. He struggles to keep his diabetes and other life-threatening conditions under control, and between he and his wife, they manage to keep him out of trouble and more importantly, out of hospital.

In recent times, Jim has been noticing changes with his eyesight. He consulted an optometrist, who decked him out in some flash new glasses. He was told that he needed to have further examinations, as there was some abonormalities that were detected.  After several appointments with opthamologists and other specialists, it appears inevitable that eventually, Jim will lose his sight.

His wife administers three lots of eye drops several times a day to reduce the photo sensitivity that he experiences. They work through every problem that comes their way. Despite the fact that he endures pain and discomfort, and fear of his unknown future, he is still willing to try anything new, and to “see” as much as he can before his occasional bad days become more frequent.

He has many really interesting and thought-provoking ideas, and he has decided to share them with the world on his new blog, entitled http://sweetbittersurvival.wordpress.com/ He also candidly shares how his dreams have been altered without his permission.

It’s more than your average diabetes yarn. His optimism and confidence are truly inspiring, and for those looking for a read with a twist of sweetness and light, fighting spirit, hope, courage and determination, Sweetbitter Survival will not disappoint. His refusal to give in to his diagnoses is nothing short of awe-inspiring.

 Go visit his site and tell him how amazing he is!!! 🙂

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