Blog Entries With Tag: Life


Posted: Apr 17, 2012


Katia is an amazing young woman that I met on the weekend at the Montreal JDRF Research Symposium..  She's currently at Concordia University here in Montreal completing a Bachelor of Fine Arts degree.  In the meantime, with her busy life, she managed to produce a documentary that takes place over 4 years.  It shows the highs and lows of herself and other teens dealing with their Type 1 diagnosis and was filmed in Canada/USA and Ecudaor.


She was sweet 16 in 2007 when she received the diagnosis of diabetes.   Of course, it was devastating to her to discover that she was diabetic (who isn't?), and she went into abit of a slump dealing with how it was going to affect her life.  It was something she knew that she could never get rid of and she decided that the best way to accept it was to take control of her life and one of those steps I feel was working on this project - which when you see the clip - you will be anxiously awaiting for the release of it next month.

She is quite the adventurous gal (she's like my D-twin) - in the way she takes life to the fullest.  Just within a year of diagnosis - she went to Europe by herself for 4 weeks - and discovered that nothing could stop her from doing what she wants to do in life.  Her next adventure was in the summer of 2010 at the age of 19 - she volunteered at the FUVIDA camp in Ecudaor - and she's now done this twice - and hopes to return again this summer.  Despite knowing very little Spanish - she managed to help others there with their diabetes. 

One part of her speech really perked my interest was the Austalian group called Insulin For Life (IFL) - along with the Diabetes Hands Foundation (DHF) provides insulin at the camp in Ecuador.  According to Neil Donelan of IFL - 10 million vials of insulin are produced every year and sadly 1 million vials go to waste.  That left me so angry - hearing this - and of course - as I discovered a few years ago - Banting never wanted insulin to be a money making drug - he wanted it available to EVERYONE that needed it to stay alive with diabetes.  Sadly, this is not the case, as other countries outside of Canada saw the money making potential (sigh) - and now - those of us who are unable to obtain insulin suffer - without insulin - we die.

I can tell that she has a very supportive family - as they were in attendance at the JDRF symposium - something I sort of envy since in my days - groups like this were very rare - and I'm not even sure if my parents would have joined up - since diabetes didn't seem to be a serious thing that I had (or that's the impression I get sometimes).  Seeing all the families at the JDRF events really gets me all pumped up - with meeting up with kids - showing them that you can lead a great life with diabetes (and yes - it's not always rosey - but what life is - that's what living is all about).

Anyway, I see great things for her future - she laughed when I told her that she could be our Prime Minister one day - to her - film making is all that she wants to do in life - but like I told her - you never know - I mean Arnold Schwarzenegger has done a few things in his life time besides flexing his biceps !



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Posted: Sep 8, 2011
Okay - if you've never heard of CouchSurfing - here's the low down - you register at the website - and viola - when you are going on your worldly travels - you can connect up with other like minded souls and the following statement says it all  that is posted at the website - "CouchSurfing is turning a missed train into an opportunity for a new adventure. Starting a weekly dinner party. Teaching your kids about other cultures from your home. Getting advice for your next trip. Engaging with the world in a whole new way. ".  So far, since registering a few years ago I haven't taken advantage of it, more so, because my DH isn't too sure about opening up our home to "strangers" - but I think I may have changed his views on the long weekend past.

I finally met up with Ginger Vieira back in July when we "performed" in her friends Dana Heffern's show called "The Antidote".  We only got to spend abit of time as she was having to head off to the DLife headquarters in Connecticut right after the show that night but she offered me her place to stay as I wasn't feeling like making the 3 hour drive back to Montreal!  Sadly, I'd already booked a little motel nearby the college - but I felt so overwhelmed by her trust in allowing someone she really didn't know - to stay at her place.  We really only knew each other through the D-OC (Diabetic Online Community) - that was it.

Last week on Facebook, she was mentioning that she was coming to Montreal for the long weekend and asked for some suggestions of places to stay.  Guess what? I offered her and her friend Allison Schauwecker to stay at our house (on the condition they take care of our rug rats aka pusscats since we were going away sailing on Jenna's Journey) - the cats need their slaves! 

It was fun getting the house ready for my visitors from abroad - even better it gave me an excuse to clean (yuppers I'm not a big fan of getting rid of dust bunnies they are meant to be free).  Now, was it because both of them are diabetic that I was enjoying this usually much despised chore?  All I know is that it made for neat to put out little things like juice boxes beside their bed stand, spare bits and pieces (e.g. - if they needed insulin - they just had to go into the "Deli Drawer" of the fridge) that I knew we diabetics need!  

If I'd had more time, I would have made gluten free bread for Ginger (psst - did you notice the September issue of Chatelaine - with GLUTEN free recipes?).

Anyway, coming home on Tuesday, I knew my cats had been taken care of by two lovely young ladies (Mia was spoiled by Ginger) and the beautiful flowers in my kitchen that they had left.  Along with some great little notes that I'm keeping forever really made me smile and appreciate what the D-OC has brought into my life.

As Ginger/Allison wrote in one of their notes to me .....




So, if you're ever visiting Montreal - need a place to rest your weary head at night - you know who to contact - Diabetes CouchSurfing!!!
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Posted: Aug 8, 2011

This blog is dedicated to my Mum – who thought my last blog – The Antidote was written while I was having a hypo.  No Mummy – I was on level playing ground – but just having fun with writing! 

I attended my first Children With Diabetes (CWD) Friends for Life Canada International Conference and Expo in Toronto.  I lucked in on getting on as part of the staff thanks to Jen Hanson  from
Connected in Motion, though sadly, because of working, I missed out on some great discussions, which I think is what the adult (and parent) participants rave about.  So, I had no time to get fun photos, etc. but at least I got to schmooze with some of the CWD staff / DRI’s (Diabetes Research Institute) VP Tom Karlya on my first night.  I think he’ll always remember me as the pole dancer wanna be – and an “ancient” diabetic without any complications.  Most people that I met at the conference when we discussed about their child’s diabetes, and I mentioned my diagnosis date, along with my age, they were like Tom, not believing my age.  What can I say?  Good genes (e.g. Levis are my favourite) - as I blogged earlier this year – insulin is a youth preserver.

I think the most rewarding part of this whole event as I felt very much alone as a newbie to the staff as we all didn’t meet up prior to the conference starting so I felt abit like an outsider  – was meeting up with many parents / kids / young adults!   I hope I gave many of the parents I spoke to an insight on how their loved ones will turn out with the right guidance and tools at hand To me, this is what sticks in my mind the most, giving parents hope that diabetes isn’t all bad.  I always wonder how it would have been for my Mum if she’d had the support of others that can now be found on the Internet. 

I did manage to attend the closing one hour speech for about 15 minutes that was given by CWD President
Jeff Hitchcock.  I had to walk out of it though due to not liking the push for parents to put their kids on insulin pumps and CGMS’s (Continuous Glucose Monitoring Systems).  Maybe because of Jeff being American and that majority of pump users are based in that country, I found it abit too much pushing the product.  Because I was raised on MDI (multiple dosage injections) for most of my 44 years of being a diabetic – it has not caused any problems similar to what he was showing as examples.  Perhaps other discussions that I couldn’t attend over the two days did go into diabetes control by MDI – I hope so – because for many of us – using a pump is unaffordable if you do not have private medical coverage from work/government help.

So, Jeff and or Tom, if you are reading this, consider bringing me in to make a speech to parents next years events as to how having diabetes for my length of time can show that your children will lead healthy and productive lives – I have – diabetes has never stopped me from doing anything I put my mind to!!!  I promise not to do any pole dancing :)


Picture credit below - Nicole Pitre-Cozad from
We CARALot Blog


Photo credit - Frank Mannella of Animas Canada

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Posted: May 11, 2010


I guess you would say that I've got a horse shoe up my ass as far as hypos or lows go.  As a child I was probably running in the medium / high range for blood sugars (BG's) since in those days generally we only injected once a day with a long acting insulin.  No fancy stuff like today with basal (Lantus/Levemir) or bolus (NovoRapid/Apidra).  Also, A1C's weren't available to the general public until the late 70's and urine testing at home was the only way to see how you were doing (depending on how long that urine had been sitting in your  bladder <lol> ).  Having low BG's really only started to effect me when I entered into my 30's  and I decided to become  more tightly controlled with MDI (multiple doseage injections)  with testing my BG's more frequently.
 
My Mum used to pack Sunmaid raisins into my school bag for those times when I might need a low.  I still love those today, but I try to be careful when I am having a low, that I don't eat too many!  I'll have a few nuts / cheese afterwards to offset all the sweetness and hopefully cause less tooth decay.
 



My other favourite treat when I'm low as a child was Life-Savers.  We all know 4 of those sweet little candies equals 15 carbs but the only problem with these, it is hard to stop at just 4!  The next colour could be my favourite flavour (green). Shovel, shovel, shovel!!!  Rebound later on :(

Life Savers


Urrrhhh!!! Now you see why I detest hypos along with leaving you like a limp noodle.  I really don't have any favourite type of food to deal with them - Dex4 is pretty well what I carry with me all the time or a juice box.  I just don't like being low, plain and simple, I'm not myself and it's a fight to struggle back to normal.  Also, to have a bad low, and being semi-comotose  at the same time  I   don't usually recall what the heck I'm eating.  Ugh!
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From: spark

Posted: Dec 23, 2009

Having never undergone any major surgery since I was little, wherein I had been hit by a motorcycle and thereby needed stitches, I was rather curious as to what life would be like post-being cut open.  In my search, I found two rather interesting (and somewhat relevant) articles..

The first is a news article released about an hour ago.  It details a man in Idaho who suffered 10 weeks of pain/stiffness because doctors had left a broken device in his knee during surgery.  Though the event occurred in 2007 and the device was eventually found and removed in 2008, it made news today because a lawsuit was just filed by the patient, naming the two doctors responsible for the mistake (Buoncristiani and Pletcher), the Sawtooth Orthopedics and Sports Medicine (where the two doctors practice), and St. Luke's Wood River Medical Center (where the surgery was initially performed). 

Eep. This article makes you realize that something to think about before undergoing surgery is checking up on your surgeon.  Getting recommendations might be the best way.... Just saying.

Anyways, the second article is much more interesting.  It was a humorous, personal account of life after surgery. The author, Michael Gibbons (managing editor at Aiken Standard) recounts the haze and daze that follows surgery. I found it rather well written and gives you a pretty good idea of what it would be like to come out of surgery.  I can only imagine that "drug-filled haze" would be the best way to describe it.  Anyone else have any thoughts on what it would be like (mentally) to come out of surgery?

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