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Kelly Kunik's Diabtesaliciousness Blog 1st entry

Kelly Kunik's Diabtesaliciousness Blog 1st entry
So After much hesitation, I've decided to join the world of blogging. What will I talk about??? Well I'm not really sure, but I do know that much of my blog will focus on the wonderful world of Type 1 Diabetes. In my world we call Diabetesaliciousness. Why? because it sounds much cooler and sexier than Type 1 Diabetes, and let's face it, it has nice a ring;)

I'm a type 1 since forever and I poke fun at all the funny things that can happen to you when your diabetic. Laughter is wonderful! But my humor is based on fact and I use not only to educate my audience, but to make them see all the positives in what can perceived as a very negative situation.

What really got me going regarding blogging was Halle Berry's most idiotic statement that she
(and I quote)
" I've been able to ween myself off insulin through diet and exercise and no longer considers myself a type 1, but a type 2."

OK PEOPLE - THAT INFORMATION COULD KILL SOMEONE.

First lesson in this blog - There is absolutely no way in hell that a Type 1 Diabetic can become a Type 2. THEY ARE 2 DIFFERENT DISEASES.
Type 1 is an autoimmune disease where the body's own cells actually attack the area of the Pancreas (The Island of Langerhans) where insulin is produced. TYPE 1's no longer make insulin and must inject the hormone in order to live.
Type 2 Diabetes is an metabolic disease where the body is insulin resistant. It still produces the hormone, but does not produce enough of it. type 2's take either oral medication or injections of the insulin.

Those of us with Type 1 or, who work and or who have a loved one with Type 1 spend 100s of hours educating any and all who ask what the difference between the two is.
A celebrity ( in this case a one who was misdiagnosed initially) spreads the falsehoods regarding the two diseases and that could cause serious harm to the public.

Do I think she was misdiagnosed? Yeah, absolutely, 100%, I do. Do I think her statement was idiotic? Yeah, absolutely, 100%, I do.


I plan to post more on the subject but my blood sugar is getting low and I need to eat.
Keep the faith and we will talk about this later.

D-Blog Day, Blogaversary, and Halle B

D-Blog Day, Blogaversary, and Halle B
So today is D-Blog Day – and by sheer coincidence, it’s also the one-year of my blog Diabetesaliciousness, which I find really “ironical” and very strange.

The whole reason I started blogging was because I’d read the infamous Halle Barry Statement regarding diabetes while I was catching up with Perez Hilton's blog. After days of commenting, along with hundreds of others on Perez’s post - 655 comments to be exact,
I became so angry. I Googled to find out who Halle's Publicist was, and called said Publicist's L.A. and NYC offices. After several rounds of voicemail tag, she & I spoke.

She basically said,Halle was misquoted, the Actor’s Studio did a butcher job on the editing, and that Halle was upset, that I was upset – but never comments on her health publicly.”


After that phone call, I became so incensed, I decided to start my own blog.

When I wrote my first post, I had no ideal what I was getting into, or what I was actually doing. I relied solely blind faith and I’m so glad I did!

127 posts later, I’m still not actually sure what it is I’m doing. But, I Do KNOW what being a member of the Diabetes O.C. has given me. It’s given me friends; laughter, information and knowledge regarding my disease, a stronger voice and confidence regarding my proficiency as a t1, and a soapbox to stand on.

Thank-you dBlogville, for sharing all the good, the bad, and the diabetes of it all. I love each and everyone of you, and appreciate your words more that you could ever know.

And thank-you Meredith O'Sullivan (Halle Berry’s Publicist) for doing your job and refusing to give me a straight answer – which of course, made me so nuts that I started to blog.

Thank you Halle for, well,.....YOU KNOW. Maybe someday you and I can actually talk about the whole thing because I'd really love to hear your side, instead of your Publicist's spin on things. I think we all would.

Happy DBLOG DAY & It's my Blogaversary!

So today is Dblog day- and it’s also the second anniversary of Diabetesaliciousness -which blows my mind on so many levels. Two years ago I had no idea that the Diabetes on-line community existed. Then Halle made her "wean myself off insulin statement” and I started to Diabetesaliciousness because I didn’t know how else to express my frustration.

I had no idea that my first entry would be on “dblog Day” and I had no idea that such wonderful and kick-ass people existed in the world!

Look, I’ve never been a shrinking violet, (wait, I take that back- the middle school and high school years did number on my self confidence and I didn’t want to talk,let alone be seen) and Diabetes blogging has given my loud alto voice a wider audience and another venue to speak regarding life with the big D.

But more than that, blogging about diabetes has given me friends (That would be you) who get where “I am,” understand where I‘m going, and have been where I’m coming from – And not just “diabetically" speaking ;)

I’ve never been shy about my diabetes or my attitude regarding living with it. I never tried to hide it from friends or classmates because hiding from who I am was never the kind of person I wanted to be.

But to be part of a community that I can turn to 24X7, 365 days a year is an amazing thing.

While I work very hard to OWN my disease and let go of the guilt, there are moments when diabetes leaves me flustered, annoyed, laughing and in tears…sometimes it’s a combination of all of the above.

And then I read about what others are experiencing and I not only recognize myself in their words, but I learn from them as well.

I learn about the obvious stuff, like medical breakthroughs, WDD Events, health care reform, and Diabetes Police frustrations.

And then there’s the not so obvious stuff, like that some people love bacon more than I do, that I’m not the only one with doorknob/pump issues, and that certain things (like cupcakes) cross both national and international lines of bolus worthy foods.

I learn from type 3’s just how difficult their connection to diabetes is.

I learn that type 2’s that their frustrations and hardships are just as difficult as mine.

I learn from the 1.5’s that they do indeed exist and that the road the walk own leads to mine in the end.

I learn from my fellow Type 1’s that my diabetes idiosyncrasies are real.

And I learn from everyone connected with Diabetes that I’m not alone.

I see myself, and the person I hope to be in everyone’s posts.

And every day I think about a person in my life who would have benefited most from the Diabetes on-line community- but who will never get the chance to experience it- and that makes me sad.

And it’s her memory that makes me think of all the PWDs who have yet to reap the benefits of what Diabetes blogs have to offer. And that makes me sad and frustrated. Every single one of us needs to continue to work on spreading the word and empowering people with diabetes.

Every person with Diabetes needs to know that they are not alone, and that there's a place right here on the Internet, where they can find knowledge; compassion, humor, and ownership of one’s diabetes.

And when you mix all those words together,they spell L-O-V-E.

And lets face it, there’s no greater feeling in the world than Love of self (faulty pancreas and all) and love of ones community~

LOVE ROCKS- AND SO DO YOU!

It's My 3rd Blogiversary & Here Are 6th Things I Want You To Know About Diabetes On D-Blog Day!


I can’t believe that the blog is 3 years old!! It’s seems like only yesterday when I wrote my first post and was a raving & ranting lunatic about The Berry weaning herself off insulin!

When I started, I had no idea what I was doing, or that there was such a huge (and awesome) Diabetes On-line Community. I just needed a place to vent and I’d heard rumblings about this thing called “A Blog.” And the fact that setting up a blog was so darn easy, I took the plunge! I didn't have much on-line etiquette at first, and it took me a while to discover the DOC, but I'm still here - and loving every minute of it!

Blogging about diabetes has given me a community, reignited my diabetes passion to inform and educate others about living life with diabetes, and it's steered my career in a Diabetes centric direction and focus.

I'm still not always quite sure what I’m doing, but I do know that whatever I'm doing, I'm doing so with a passion and I’m so grateful to be part of such a fantastical and powerful community!

Over the past three years I’ve learned so much from others regarding both diabetes and life. Blogging has made me a better person, a healthier person with diabetes, and blogging has enhanced my writing skills. Diabetes Blogging has also made my voice louder than I ever thought possible! Which is pretty damn loud considering that I have quite a set of lungs!

So thanks for reading, supporting, giving me your shoulder to cry on when needed, always making me laugh, and continuing to teach me something new every day.

And thank you for making me strive to be better and achieve more in every aspect of my life.

I love you guys so much!

BTW, I just read that Rachel over at Tales Of Rachel is celebrating her Blogaversary today too! 5 years of blogging - OUTSTANDING! So go on over there and wish her a Happy Blogaversary!

Today is the 6th annual D-Blog Day - I kid you not! Gina created D-Blog Day in order to unite all the diabetes bloggers and to educate the public about diabetes, during National Diabetes Month! Good job Gina!

This years D-Blog Day theme is: 6 Things I want you To Know About Diabetes.

Here Are The 6th Things I Want You To Know About Living With Diabetes!

  1. Diabetes is NOT a character flaw. While it’s true that many characters have diabetes, including myself. Being a person with diabetes doesn't make you a bad person, a terrible judge of character, a lazy sugar addict, or person who lacks quality.
  2. Being a person with diabetes does not make me weaker or less capable of working and living a full life. Yes, there are times when diabetes makes me feel like crap, but that doesn’t make me any less capable- on the contrary, it makes me more determined then ever to do a great job and live a great life!
  3. Don’t ask a person with diabetes “Are you sure your allowed to eat that?” because like the rest of the population – we can pretty much anything – in moderation. Seriously, I don’t know many people over the age of 30 who can eat whatever they want, so stop judging us on what we put in our mouths. Instead, why not ask: Is your diet restricted because of diabetes? OR I’m totally confused by what a person with diabetes can or can’t eat. Can you explain it to me?
  4. As a person living with diabetes, I’m constantly doing Diabetes Math and calculating the carbs of every scrap of food I put into my body so I can figure out how much insulin to take to cover that food. This makes me good at multi-tasking. Not because I want to be, but because I have to be. So next time you and I are out to dinner and we’re deep in conversation, keep in mind that I will secretly be eyeballing and calculating carbs while gushing over your child’s baby pics or laughing at your last nightmare blind date!
  5. There is NO CURE FOR DIABETES. Yes, insulin allows me to live, but insulin is not a cure. I’m alive because of insulin, but if I don’t take my insulin, I’m dead, “sleeping with the fishes,” Je suis morte, & fini. And even with insulin, I'm still at risk for all type of diabetes complications.
  6. Finally, If you have any questions about diabetes, don’t be afraid to ask, because that’s what I’m here for! After 33 years of living with type 1 diabetes, I know a thing a two about the subject! And in all honesty, I’d rather you ask a diabetes question then continue to perpetuate diabetes myths or stereotypes!

A healthy child, vaccination, a damaged child, homeopathy, a child getting better

A healthy child, vaccination, a damaged child, homeopathy, a child getting better
This video tells a story. Starting with a healthy child, who is vaccinated, who becomes autistic, who is treated with homeopathy, and is beginning to get better.

Please, watch this video; it covers everything in 9 minutes; the dangers of ConMed, the potential destruction of a child's life, a family's sorry and anguish, and how homeopathy is helping the child to recover. With film of the child at every stage.

http://www.kickstarter.com/projects/1390762414/from-within-without-a-documentary-about-homeopathy

A Novel Treatment for Brain Cancer?

A Novel Treatment for Brain Cancer?
Research undertaken in 2003, and published in the International Journal of Oncology (23: 975-982, 2003) found that Ruta 6 (homeopathy remedy at 6c dilution) "selectively induces cell death in  brain cancer cells but proliferation in normal peripheral blood lymphocytes" and described the remedy as "a novel treatment for brain cancer".

You can see the full paper at http://www.virtualtrials.com/pdf/ruta6.pdf

How strange that little more has been heard of this! Perhaps there is no profit for drug companies in diluting Ruta Grav.

Shuuusss. No-one is supposed to know that homeopathy works .......

Homeopathy. 70% report positive health changes

Homeopathy. 70% report positive health changes
70.7% of patients using homeopathy reported positive health changes, with 50.7% recording their improvement as 'better' or 'much better'.

You can find this study at
http://www.britishhomeopathic.org/export/sites/bha_site/research/JACM_11_5_p793-798.pdf

The study sought to assess health changes observed following routine homeopathic care for patients with a wide range of chronic conditions. It was a large observational study of 6,544 patients taken over a 6-year period.



Epilim; a dangerous drug, but no legal redress for families

Epilim; a dangerous drug, but no legal redress for families
Dozens of families who blame an epilepsy drug, Epilim, for causing birth defects in their children (see information on FACs) say they are devastated that legal aid to sue its maker has been withdrawn. So says a BBC report at:
http://www.bbc.co.uk/news/uk-11707386

What is important in this story is not just that no patient is safe taking ConMed drugs, but that drug companies don't admit that their drugs have done anything 'wrong', and, in the UK, the government does not enable families to take such matters to the courts. There is little justice.

So it would seem that UK patients have to be even more careful than those in the USA. In the USA, 'class actions' against drug companies are regularly passing through the legal system, so at least those who have suffered disease and death have some access to justice, and drug companies have been forced to pay many $billions in compensation for the suffering and distress they cause.

The families concerned have children that have suffered because Epilin by the mother during pregnancy. This has caused their children to be born with spina bifida, heart damage and learning difficulties. Their lives have been devastated by ConMed drugs.

And it would appear that in the UK the drug companies, the government, and the NHS are not prepared to take any responsibility.

Multaq is a dangerous drug

Multaq is a dangerous drug
Multaq has been around a couple of years now. Initially it was supposed to show such fantastic results the FDA in the USA 'fast-tracked' it for approval. Then, of course, after 1000s, millions of patients suffer, the truth begins to trickle out. The drug is dangerous. It causes disease, and death.

But nothing is done, immediately, of course. The evidence of harm has to be more extreme, or experienced over a longer term. Patients are not told anything other than that "the benefits outweigh the disadvantages".

Pharmalot has now outlined the short history of the drug at  http://www.pharmalot.com/2010/11/heartstopping-news-more-multaq-safety-signals/

" Since its approval last year, the Sanofi-Aventis Moltaq heart drug has been controversial. For instance, a study published last spring found the pill is only modestly effective and has not clear safety benefits and more recently, questions were raised about the study that led to FDA approval.

Now, a new analysis of FDA adverse event reports indicate Multaq may cause or worsen heart failure, trigger potentially lethal irregular heartbeats and impair kidney function. There is also a glaring discrepancy between the language in the Med Guide given docs and patients, and the warning label about pregnant patients. And the findings led The Institute for Safe Medicine Practices, which conducted the analysis, to conclude that “we have seldom seen a drug with so many issues in so many areas of its safety profile.”
Why? The non-profit points out that development stopped several years ago after a study of patients with severe heart failure found the drug doubled the risk of death; other data found signals of cancer and birth defects in animals; there are potentially serious interactions with other drugs used to treat atrial fibrillation, and Multaq causes new heart rhythm disturbances in some patients.
The report goes into more detail about the findings, but what is important is what this story tells patients. This is a relatively 'new' drug, so 'good' that the FDA wanted you to have it as quickly as possible. Within less than 2 years, serious disease-inducing-effects (DIEs) have been reported.

But patients will not be told. Nor will the drug be withdrawn, at least not yet. It might take a decade for this to happen. Big Pharma is the only industry allowed to peddle dangerous merchandise to customers which are unsafe, and are given the benefit of the doubt. They may purchase 'scientists' to provide spurious evidence of safety. The medical science never protects patients from these drugs.

Imagine what would happen to a car company if they produced a succession of cars that proved to be unsafe! The company would be in big trouble. People would not buy their cars. The mainstream media would publicise the dangers, and warn the public. The government would demand action.

But none of this happens as far as Big Pharma drugs are concerned. Their products are considered 'safe' until they are proven to be dangerous. They are treated in exactly the opposite way to any other industry.
AND IT IS OUR HEALTH THAT IS AT STAKE HERE!

This blog will keep an eye on the future of this drug, which if it takes a normal course will end in the drug company withdrawing it, or the FDA banning it. 

Yet for many patients, this will be too late. So anyone who knows about these 'early' problems should take sensible precautionary action now. I suggest that they tell their doctors they are not prepared to take the drug, and demand to be told the whole truth!

BMJ say Statin drugs cause liver damage, kidney failure and cataracts

BMJ say Statin drugs cause liver damage, kidney failure and cataracts
Statins? That's the drug doctors have been telling us is so safe everyone should be taking, isn't it? Now, the BMJ have published evidence that admits that it causes disease!

Well, better late than never. But even better if it was 'never'. What this proves is that you cannot trust ConMed medication. You cannot trust medical professionals who tells you they are safe. The government, the NHS, Big Pharma are not prepared to tell you UNTIL it is proved that people have suffered. And unfortunately, our doctors are quite prepared to go along with this charade.

Natural News published this on 7th November 2010, where fuller information can be found, with references. The research was done at Nottingham University using data from more than 2 million patients taking Statin drugs.

There are safer ways of protecting yourself from heart disease, and this includes homeopathy; not to mention a sensible exercise regime, and a good diet. Statins are useful mainly for the profits accrued by the drug companies. As the piece concludes, these profits are not going to be compromised!

Although sales of the blockbuster drugs are unlikely to be reduced as a result of the study, the researchers encouraged closer monitoring of patients for side effects and said their findings "would tend to support a policy of using lower doses of statins in people at high risk of the adverse events."

In other words, we are expected to just keep on taking the drugs!

Why Celebrities choose homeopathy

Why Celebrities choose homeopathy
This is a simple video that outlines why a large number of celebrities have used homeopathy for their conditions and ailments in recent years. It shows the variety of conditions homeopathy can treat, and the success it can achieve.

http://www.youtube.com/watch?v=XR7E7FbGpEA

Of course, this is only a selection of such 'celebrities'. More can be found in Dana Ullman's book, The Homeopathic Revolution: Why famous people and cultural heroes choose Homeoapathy.