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Diabetes hits home for Maria Menounos

Posted: Wednesday, October 08, 2008 5:20 PM by Jen Brown

From Maria Menounos, TODAY contributor

Diabetes has officially become an epidemic of national and even worldwide proportions. In the past few decades, the disease has grown at an alarming rate that continues to escalate today. In addition, there are upwards of 5.7 million people have the disease and do not even know it, according to the American Diabetes Association.
 
Maria Menounos with her parents, Stavroula and Costas.

For me, the disease and its debilitating effects have been all too familiar, as my father was diagnosed with diabetes over 40 years ago. The disease crippled our family. My mother and I were forced to monitor his sugar level 24 hours a day, and Dad’s ongoing low blood sugar attacks (there were hundreds, maybe even thousands) placed him in deadly peril.  Sometimes he would be behind the wheel when his blood sugar dropped, and he would drive off the road. Sometimes he would forget his identity, lose his bearings and wander off.  Police who misread his conditions for drunkenness arrested him.  He even slipped into a coma, and was pronounced dead by doctors.

Thankfully, I was eventually able to get my father to the right physicians who could educate my mother, father and me on how to properly treat the disease. Up until that time, we were basically winging it on common sense and outdated medical advice.   With the help of the pump (a device that continually monitors sugar and delivers insulin) and a proper diet, I am proud to report - with the hardest of knocks on wood - that my father is doing better than ever.
 
We are not alone
I pitched a series on diabetes to NBC because I know there are so many other families out there struggling with the disease and perhaps unnecessarily so. When I first started at The Today Show I did a two-minute story on the subject. It was a step in the right direction, for sure, but two minutes is simply not enough time to adequately raise awareness for a condition of this magnitude.

With the diabetes series that kicks off on Thursday, we are not only going to explain the differences between Type 1 and Type 2, we are also going to conduct a Diabetes Fair on The Plaza. At the fair, people will have the opportunity to meet with the best nutritionists, doctors, trainers and educators. Individual testing for the existence of the disease will also be conducted. Perhaps you are one of the 5.7 million people who have been unknowingly living with diabetes.  The fair will be the place to learn about treatment.  The disease is actually manageable and if you’re afraid that you could have it, this is your chance to be exposed to the best of the best in terms of practitioners.

Those of you who may need to lose weight so your Type 2 diabetes doesn’t advance to the stage of insulin, I urge you to come on down to the plaza and have the best fitness experts put you on a plan for a better tomorrow. For those with Type 1, my dad’s personal physician, Dr. Anne Peters, will be there to help answer your questions. She single-handedly saved his life. Simple changes to his daily regiment made the difference. I want that same difference for you.
 


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Thank you for providing this very necessary awareness.  Type 1 diabetes is indeed relentless and potentially crippling.   I hope your next series will focus on what areas of research are working towards a cure, or at least restoring euglycemia for persons diagnosed with type 1 diabetes.  

Of particular interest to me as a parent of a now 20 year old who was diagnosed with type 1, 19 years ago, is encapsulated porcine islet research.  I hope that LCT will be able to bring their research from New Zealand to the United States and begin human clinical trials.  They currently have human clinical trials going in Russia.  There is no shortage of pig islets.  And encapsulation means NO toxic immunosuppression.  We must fund, test, and improve upon this research.
A friend of mine called me all excited about the diabetes portion of your show today.  She said the symptoms described souded exactly like the problems I've been having lately. Drs. here keep checking my blood and telling me everythings fine. But it isn't!! I really need help in finding some answers. Can you PLEASE give me some advice?   Thank you
P.S.  I've had hypoglycemia for many years, lately it's become much more severe.
I would love to personally thank Maria for speaking about diabetes this morning on the today show. It was very insightful and educational. It totally hit me from all angles of emotions since I have been diabetic for over 40yrs. I was diagnosed at age 11. I truly did think I would be here today. We do need to get more people talking about this disease. I would be more than happy to go on a talk show and discuss my disease and bring awareness to the challenging disease. I am on the pump and this has allowed me to have better control and freedom with this disease. When I tell people that I'm diabetic and for how long they are in disbelief. But this is a very debilitating disease that is deadly and one must respect it.
I want you to know that you did a wonderful job today!  I am not going to be as clear as I would like because of the tears I am going through right now!  It is about time a major news organization gets it right!!!!!!!!  Thank you thank you thank you!  

Nicole
Mom of 12 year old with Type 1 diabetes diagnosed Friday October 13th of 2006
The importance of knowledge of the disease can not be understated. Also maintaining good glucose control is terribly important to avoid the terrible complications of the disease. For great information on the self management of the disease and all the latest news please visit www.DefeatDiabetes.org
Maria, thank you for this! My wonderful 14 yr old granddaughter, Katie, has had type 1 since she was 11. She is on the pump and does well, but it is a constant battle for both Katie and her mother.She is forced to miss many days of school and that causes stress for her. I am so glad your Dad is doing so much better. Is there any new information on research and a cure?
Again thank you!
Great post -- I have had Type 1 diabetes for 42 years and can identify so much with your father -- my family and I were not educated  in re: diabetes wellness and as a result I lost my sight in my early 20s. Now I follow my diet, take regular injections of insulin, exercise (I walk miles every day with my Seeing Eye dog and I swim laps at the pool) and despite my blindness I feel GREAT. I have a new life as a published author and freelance journalist (I use a talking computer, am using it now to send this message) and appreciate your stories about diabetes -- especially when you explain the differences between Type 1 and Type 2. Thank you, and keep up the good -- and important -- work.  
Kudos to Maria and NBC for covering this important topic.  I have had Type 1 diabetes for 33 years, and know all to well how deeply this disease affects people and their loved ones.  I have struggled with different complications over my life, and continue to worry about my future and how I will survive this disease.

Most importantly , it is time for a cure!  Insulin is not a cure, and we must continue to take this disease seriously and fund research appropriately!
maria,
i'm glad to see that your father is doing better in managing his diabetes. My son became diabetic at age 3yrs.  His DR did not catch it after 2 visit, I caught it on my own, after reading the medical book about his symptoms and demanded that they test his urine. they wouldn't without a DR's order, but I stood firm and told them I have a very sick child at home and your DR can't figure it out but I can! Sure enough he had sugar in his urine, and ketone's.  I took him to Children's Hospital, and that changed me forever, it was like learning that your child has died and became a new person with a disease. I couldn't sleep with my husband, I had to be with my son day and night, watching him since he was only 3 yrs old!!  The whole family suffered with this, becuase I was a wreck dealing with it at first, then I focused all my time on it, learning, and caring for him. It got easier as he got older, he was able to tell me how he was feeling and if he needed to eat or needed a shot of insulin.  Now he is 15 yrs old, taken trips on his own, managing it himself and very active in his life!  KNOWLEDGE IS POWER!
You gave some statistics on Diabetes and how it may progress in the future/future generations.  Where can I find these statistics?
thank you
Maria's story this morning made me stop in my tracks.  This hit SO extremely close to home.  As a 26 year old, who also grew up in a home where my father had Type 1 Diabetes, I have horrible memories of ambulances, passing out, driving off the road and my father even going into a coma.  Since then he also has received the Insulin Pump, and while is has helped, it's still an every day struggle.  If my mother wasn't around, I firmly believe my father wouldn't be here today.  

Thank you, Maria for sharing your story and showing the world about Type 1 Diabetes.  
Thank you for talking about type 1, we hear so much about type 2 it was nice to hear type 1 addressed
I married my husband in 1973. He had diabetes since he was 12.  I never knew how bad it was.  He constantly was having low sugar attacks.  They scared me to death.  He had a terrible time controlling his blood sugars.  He passed away 8 years ago.  He was only 51.  Very sad.  Had every side effect possible.  I wish somebody could find a cure for this disease.  It is so hard to live with.
It is not easy to be told to be on a lifetime diet.
Maria,
Thank you for your focus on diabetes. I am g-ma to a 6 year old with type 1. His diabetes is so out of control and the Ins. won't pay for a pump. He is so tired of shots, this is a former conversation from he and mom. Judah,"mom, I want to be normal", mom, "Judah you have to take your shots to stay   healthy ", Judah, "well what happens if I stop", Mom,
"you will die honey", JUdah, "HOW LONG WILL IT TAKE".
This breaks my heart that a 6 year old is thinking it might be worth it just to be normal for awhile. He was diagnosed at 2 1/2 and has been dealing with this a long time. Poor baby,ended up in the hospital because his teacher wouldn't let him have water in class. They need alot of water to flush the sugar from their bodies. His kidneys and liver were shutting down. You are right, type 1 can be a life and death situation everyday. We do JDRF walks to raise funds, lots of vendors there to support us and guess what....there wasn't a pharmaceutical company on site. We pay alot of money for supplies and insulin. You would think they would be out there supporting the walkers and victims. Not so.
Thank you again for talking about this topic on the Today Show. Vicki, Grandma to Judah.


Thanks Maria.  I loved your segment about diabetes. My son was diagnosed with Type 1 at age 2, and my brother and two aunts all have Type 1 as well.  I'm so happy more and more people are talking about this disease. I know a cure is out there, we just have to find it.
Hi Maria,
I was so touched about your story on the Today Show about your father's battle with Type 1 Diabetes.  I know and understand all that you and your family have gone through.  I have a 5 year old daughter that was diagnosed with Type 1 diabetes at the age of 3.  It has completely changed our lives.  I remember the day the doctors told us, it feel like the whole world came crashing down.  It is amazing how much diabetes affects your life on a daily basis.  It affects EVERYTHING she does.  There have been many days she has missed recess with her friends, because she did not finish all her lunch, so to avoid her hitting a blood sugar low, she has to go and finish eating in the nurses office.She was recently in the hospital because she got a virual infection and it affected her diabetes and in order to get them back in control, the doctors had to put her in the hospital. People that diabetes does not affect their lives on a daily basis have no clue what it is like either be living with diabetes or having a family member that you love dearly have diabetes.
I commend you coming forward and making people aware of this awful disease.  I agree that every person in America should be checked for diabetes or pre-diabetes, it is amazing how many children and adults it affects in this country. Too many people think, "There is not a family history of diabetes in our family, so I won't get it." We don't have it in our family and my daughter has diabetes. Did you know that 85% of all people that have diabetes, there is no family history of the disease. We have to educate American's about this disease and keep raise money for find a cure.
Thank you so much to you and your family for coming forward with your personal story, that not only touched me personally, but I am sure many others.
I was so happy to see the discussion between Type I & II Diabetes.  I have been a Type I Diabetic since age 9, I am now 42 years old.  My Father was diagnosed with Type I diabetes in his early 20's and one of my sister's was also diagnosed at the age of 6.

There have been so many times that all of us have had life threatening episodes, it is frightening for us as well as our families.

I hope that there are more discussions on the difference's between Type I & II Diabetes and that people realize that being a Type I Diabetic has nothing to do with an obesity problem, our Pancreas does not produce insulin period.
FINALLY a story revealing the day to day obstacles of Type 1 diabetes! Imagine waking up each morning and trying to guess how your day will go; will you be more/less active than usual, will there be any additional stress, are you catching a cold, will you have enough time to eat; will you eat more/less than usual? Despite your best efforts many days to not go as planned resulting in high or low blood glucose levels.
A lot of attention has been placed on Type 2 diabetes and it has been stressed that it is on the rise due to obesity; rightfully so, however much of the general public now assumes that people with diabetes "deserve" it due to their unhealthy lifestyle.
My son Jimmy was diagnosed with Type 1 diabetes when he was 13 months old, he is now 11 years old. We have experienced much of what Maria described. I have held my son through seizures while he lay in my lap; fetal position, eyes rolled back in his head and making a 'choking' noise. I have held him while being transported by EMS to the hospital and laid beside him while hospitalized. These are not unusual occurrences but typical for anyone living with Type 1 diabetes.
Because people do not understand the magnitude of diabetes care at school has been a challenge. Only after a teacher and the secretary's husband was diagnosed with diabetes did my son receive minimal care; daily glucose testing with the health aide. I worried a lot of days when I sent him off to school. Jimmy has recently began using the insulin pump with much success. He no longer needs his afternoon snack at 1:00 to counteract his insulin dose 'peaking', if his glucose is high he can 'fix' it without waiting in the office for me to arrive with a syringe.
There is much, much more I could say, however I'll close in saying THANK YOU for shedding some light on this challenging, not to mention, deadly disease.
Sincerely,
Chris
       
Maria, I saw the segment you did today concerning your dad and diabetes. I have been a Type I diabetic since I was two, I am now 48. I have been on an insulin pump for 15 years, and have two beautiful children thanks to God and the pump. I recently was put on the Paradigm pump. I love the way the glucose meter sends my blood sugar results to the pump so adjustments can then be made.There is a glucose sensor available that works directly with the pump, that will alarm if blood sugar levels are to low or to high. The problem is insurance companies do not want to pay for the sensor. They claim it is not medically necessary. My doctor has sent numerous letters, and documented ambulance and hospital records showing it is medically necessary. My question is what can be done to get insurance companies to pay for the sensor. To me the benefits of preventing further organ damage or even death due to hypoglycemia far out way the cost of the sensor. Any help would be greatly appreciated.
You can not ignore Type 2 Diabetes either.  I have had Type 1 for 35 years with no known complications and my husband was diagnosed with Type 2 a little over 10 years ago and he is now undergoing laser treatments for Diabetic Retinopathy.  Neither Type 1 or Type 2 need to be ignored, they both need to be addressed.
I am a 61 year old Type I diabetic who is also a medical device engineer. After dozens of years studying diabetes, I have concluded that management of blood glucose is extraordinarily complicated and that the expectation that a person should just know what to do at all times (based on their experience) is imposible. Therefore, tools such as the continuous glucose monitor, pumps, and others, are essential to tight control. However, the costs, complexity, and lack of insurance coverage are often prohibitive. To counter this, I am presently involved in 3 start-up companies focused on bringing simple, low cost technologies to bear on the problem. Hopefully, we can all pull together to encompass the needs of this ever expanding population of diabetics.
I have found out that ethic group need someone to translate to groups that do not speak english on what causes Diabetes and what signs to look for in Type 1 daibetes.I'm working with a program Southeast Health Disparities in Chicago, IL
I have learned alot about Diabetes through a special program that sent me to training empowerment on Diabtes. I learned how it effect your hold body and the signs to notice if Type 1 diabetes.
Maria, thank you for focusing on Type 1 Diabetes. I am tired of people assuming that I can control my disease with diet and exercise alone, "My Aunt, lost weight  and her diabetes disappeared.".  There is definately a sort of judgement towards diabetics. I had nothing to do with the developement of my disease, it was a faulty gene. Like you so eloquently said, diabetes threatens my life everyday. For years all we have heard about is Type 2 which is mostly preventable, and definately cureable.  Type 1 is a totally diffrent disease and deserves more attention.  It is 100% fatal, whether directly or because of stroke or heart disease.  I have been a Type 1 Diabetic for 33 years and like your Father, I am on a pump.  It has changed my life.  I had two healthy children, have few complications and feel like I might be alive long enough to dance at my daughters wedding, and play with my Great-grandchildren, something that was unheard of 30 years ago.  Thank you again for focusing your attention on a misunderstood disease. Type 1 diabetes its own attention, and you have started a wonderful campaign to educate people.
Thank you Maria and Today!
As the mother of an 8 year old with Type 1 Diabetes I thank you from the bottom of my heart for highlighting type 1 diabetes for a change.  Seems that the world knows all about Type 2 but no one pays any attention to type 1 and the misconceptions are endless.  Thanks you for sharing your story with us, and in turn helping our children.

To a previous poster - Paul - who stated that a pump i s "permanently attached to your body", I'd like to state that nothing could be further from the truth.  As Maria would point out, the pump is not permanently attached, nor is it surgically implanted.  It involves a cannula which the user changes every few days,  placed under the skin (not inside the body, simply in the subcutaneous fat under the skin) the pump is attached to that via tubing. The pump can be removed whenever needed, and the infusion site is removed when you change it without even a bandaid needed to cover it.  You do this at home - in about 30 seconds.  It's not a scary, surgical type thing, there's no blood, and the only reminder is perhaps a pin prick sized mark.  Hope that clarifies for you.
For June and Amy,

I know any new technology is scary, but I teach the pump and glucose sensor to at least 3-4 patients every weekend for the last 10 years. The one thing that "BLOWS my MIND" is how fast someone that has "crazy blood glucoses" will have a return to normally within JUST A FEW DAYS!!!! Many of my patients have awesome glucoses with fewer highs and fewer lows and of course the awesome flexiblity. My sister has been "PUMPING" for almost 27 years!!!! with great results.  So just realize DO NOT BE SCARED!!!! your trainer will be there for you and depending on the company, you will also have tech help.. YOU ARE NOT out there by yourself... Find other pumpers also to help. They are all over the internet and support groups... MOST OF MY PATIENTS TELL ME "I wished I did this sooner"..   JUST DO IT!!!
The segment was a great start but please move away from the idea that Diabetes Type 2 is the fault of the individual and can be prevented by not becoming overweight. There is a lot more to it than that and we diabetics struggle with enough without guilt heaped upon us by "experts." The wonderful website, www.dlife.com, addresses every facet of diabetes and NBC should be bringing in true experts for this series- check out the dlife site for names of many!
The Today show is a part of my morning routine. I watch it everyday while getting ready for work. I was happy to hear this morning's segment on diabetes and pumping and it aired at a perfect time for our family.  Hearing this story this morning really hit home and I'll briefly tell you why.  I have a daugter with Type 1 diabetes. She was diagnosed when she was 9.  She'll be 18 next week. We have struggled with her management for 9 years and her blood glucose(BG) levels have been inconsistent to say the least. She has been hospitalized a few times suffering from ketoacidosis (an effect of having high BG levels).   Assisting with my daughter's management has been challenging and stressful throughout the years. As parents we want to fix everything for our children and this is something we just couldn't fix and found it to be the most challenging and heart wrenching experiences.  In her early teens, my daughter went through a period of falsifying her blood glucose levels to make us believe she was doing good when in fact her BG levels were extremely high.  During this period we later learned she was suffering from diabulimia (when a type 1 diabetic deprives themselves of insulin to lose weight). It has been a hard road but we hope to open a new chapter in her life real soon.  My daughter has agreed to try the Medtronic insulin pump and will have it within the next couple of weeks.  I am hopeful the pump will assist in regulating her blood glucose levels and assist her with living a long and healthy life.  Thank you for airing this segment and a job well done Maria!  Additional segments should be aired specifically for teens and their families dealing with type 1 diabetes.  Thanks again Maria and best wishes to you and your family.
I'm so glad you are focusing attention on diabetes.  My daughter was diagnosed Nov. 14 of last year at the age of two.  It's been life altering, but she is strong, energetic and amazing.
Like most people we were unaware of how different type 1 and 2 can be.  People managing with type 1 each day can tell you it's ever changing.  If it's not already scheduled - could you talk a little about diabetic alert dogs.  We are trying to get one and these programs could use more funding to increase accessibility to more individuals.  
Thank you!
As the parent of a child who has lived with the challenges of insulin-dependent, Type 1 diabetes for six years, I felt dispirited this morning when the segment omitted an important component of the management of this chronic, currently incurable condition.  The insulin pump, while a magnificent tool to control blood sugars, is a significant financial expense that sadly many families lack the financial resources to cover.  An insurance company may pay for part of the $8,000 pump, but that still leaves a significant co-pay that many Americans cannot come up with.  In addition, the segment didn't discuss the reality that insurance companies such as Blue Cross consciously choose not to cover the costs of the pump's infusion sets that must be changed every three days in order to make the pump work properly.  Would have appreciated having either Ann Curry, Maria Menounos, or Dr. Snyderman ask insurance executives and Medtronic/Minimed executives how they justify excluding coverage of the infusion sets.  We do without many, many things now in order to cover the costs of our son's infusion sets (because no one in the process thought to disclose that they'd cover part of the pump but not the things to make it work!), and personally know others with the condition who lack the financial means to switch to pump therapy from multiple daily shots simply because they can't afford it!!
I only saw part of the segment this morning with Maria. While I am grateful the emphasis was on Type 1 (which I have had since 1995) I think some points were over simplified and some overdramtaized. Yes, I agree with several posters that pump therapy is great (have been wearing one since 1998) it doesn't magically make your highs and lows go away, the way Dr. Schneiderman made it sound. Living with Diabetes is, as others stated a 24/7 responsibility. I agree with the poster that said it's up to the person living with Diabetes to manage effectively, but I disagree with him that a diabetic shouldn't be supported by a team of doctors/health educators. And wouldn't his wife feel it easier to change a canula (what attaches the pump to your body) every 2-3 days then taking shots 3-4 times per day? This is only one of the benefits of pump therapy. There are many others that weren't talked about. Also, please please don't group Type 1 and Type 2 together! They are TWO DIFFERENT DISEASES! Type 1 is an auto immune disease and only 1 out of 10 Diabetics have this type. Type 2 is a metabolic disorder and therefore IS preventable from the standpoint that if you have genetic predisposition you can live a healthy lifestyle and significantly reduce the chances of getting the desease. Type 1 is NOT preventable since nobody knows what causes it. Finally, I have to take issue with Maria's comment that millions of people are "Pre-Diabetic". What does that mean? Is this the replacement term to what used to be referred to as "Borderline Diabetic"? Neither exists. It's makes as much sense as being "Pre-Pregnant"! Either you are or you aren't Diabetic. Thank you for bringing attention to Type 1 specifically, but you really need to do some further investigations. People can live healthy productive lives with Type 1, but it can be difficult and scary too. Maria's dad is an extreme case - and I wish him well, but for those of us who don't have the episodes he has experienced, it's still very hard work to manage, even with pump therapy.
Thank you for sharing information about Diabetes to your viewers.  My daughter was diagnosed with Type 1 Diabetes one year ago, at the age of 4.  We mourn the loss of her childhood.  She is now forced to check her blood sugar 6 times a day.  She faces many physical and emotional challenges as her blood sugars swing from high to low.  Even something like going to a birthday party affects my daughter.  She is not old enough to give herself shots so we either need to tag along to the party, or she simply cannot go.  Not to mention how her body will deal with all the food that is at the party.  Yet, we do the best we can and my daughter is one tough cookie.  I am so proud of her!
Thanks Maria, I have been fighting it for over 30 yrs. I have lost jobs, friends, trust in myself doing many things. There is no fighting it. Just adjusting is all I can do. Still life is so worth it. And I dont have a blame thing with it either. Any coverage is great. Enjoyed your Guidepost gig also.
Thank you, Thank you, Thank you. Being a mother of a child with Type 1 diabetes, I am so thankful for you doing a story that actually explains the difference of Type 1 from Type 2.  thank you from the bottom of my heart, your going to help millions!
I'm a 23 year old Type 1 that is looking forward to the next chapter of my life as a recent college graduate.  I've been battling with an onset of diabetic neuropathy/carpal tunnel over the past year.  Despite all efforts to remain upbeat and happy for life, it's been a challenge as it undoubtedly interferes with my daily life.  I'm a naturally enthusiastic and chirpy person, so it hurts more to see my own spirit fall.  It's heartwarming to read such articles and comments of others.  I don't know why but I've been bawling my eyes out reading them!  Nonetheless it's comforting but deeply saddening at the same time.  I wish the best for everyone that is in similar situations and hope for the success of the show/awareness promotion.  
Thank you so much for sharing your story with us.  My husband was diagnosed with Type 1 at 27, 3 months after we were married.  I was terrified.  We were wanting to start a family and are lives were turned upside down. There is so much to learn and it is a everyday life or death battle. He has been in the hospital once for a diabetic siezure he had in the middle of the night, he wasn't breathing well and he was shaking, luckily that woke me up.  He is in the process of getting an isulin pump and we have a beautiful little girl. Your story gives me great hope for our future.  
I watch the Today’s show everyday and as a Type I diabetic of 14 years, I was very interested in today’s segment, however, I was extremely disappointed in the message you sent out about the disease.  While Type 1 diabetes is a very serious disease and extremely important to manage, millions of people do it everyday (with and without the pump) and lead normal, healthy lives.  In fact, many Type 1 diabetics are healthier than non-diabetics due to their education about health and their constant dedication and monitoring. Portraying your family as a victim and over dramatizing the life as a diabetic doesn’t help anyone to better understand the disease, find ways to manage a normal life with the disease and/or find a cure.  The public needs to be educated on the differences between Type 1 and Type 2, the causes of the disease - as they are very different - and the fact that it’s not preventable in most instances.  It boggles my mind that someone so close to Type 1 diabetes would set the stage for this type of label on the disease which is very damaging to progress that’s been made with awareness to date.  Personally, my pancreas stopped producing insulin when I was 14, active in three sports, very healthy and had no family history of the disease – making me a Type 1 Diabetic. I have been dedicated to managing the disease very closely, visiting the doctor regularly and have maintained a normal, healthy life without the pump permanently attached to me.  
Saw your piece this morning.  My husband has been a diabetic for 33yrs.  My 51/2 yr old son was diagnosed 4 weeks ago.  They both have a pump.  My husband got his 4 yrs ago, after having his second kidney transplant.  We got my son his pump right away.  It has made a world of difference for my husband.  My son doesn't cry anymore when he needs to take insulin.

Thanks for making so many people aware of the technology that helps so many live "normal" lives.

Maria,

Thank you for putting type 1 diabetes in the spotlight today. My 13yr old daughter was 18 months old when she was DX. Needless to say I have not had one night of peace. She has hypoglycemia unawareness, basically she can not tell when she has a low. Since kindergarten she has had a nurse or aid with her at all times. This brings unwanted attention to her and makes her stand out even more. She has been on the pump for the past 6 years. It is great. Thank you Maria for bringing awareness to such a huge audience. Great job! Thank you for sharing you personal story about your father also.
I have been a diabetic for 25 years and was up to 5 injections per day.  I could not get my A1C level below a 7.9.  I went on the insulim pump last December and in three months my A1C was down to a 6.5 and now is a 6.3.  The pump is the best thing I have ever done for myself.  I did a lot of research and talking with other Type 1 diabetics and went with the Medtronic Mimimed.  I just want to stress to other diabetics.... look for and attend support groups for Type 1 and 2 diabetes.  It makes life easier talking to others who have diabetes
Your comment "With the help of the pump (a device that continually monitors sugar and delivers insulin)" is not exactly accurate.  The pump does deliver insulin but most pumps (alone) do not provide the much needed monitoring you refer to.  This has become a huge problem for me personally because my insurance has approved the pump but will not approve the "Continuous Glucose Monitoring" portion.  I've been told most insurance companies are not approving this.  Do you have any advice?
Thank you for bring the difference between Type 1 and Type 2 up front! My husband has had Type 1 for 30 years and has been on a pump for over 5 years now. He was the first person I ever met with diabetes and we have now been married for over 16 years. I get frustrated when people assume diabetes is simply the consequence of a bad diet and no exercise. I even had to explain the difference between 1 and 2 to a 911 operator recently when my husband had the flu and we could not get his blood sugar level above 23. I know it is hard for my sons (13 and 10) to explain to their friends why their Dad acts goofy sometimes or why he suddenly gets angry for no reason. My husband tries to keep a good attitude but it is hard - he was recently also diagnosed with MS, another auto-immune disease. I cannot stress the importance of self-education and determination - sometimes getting the right treatment requires hours of paperwork and phone calls to convince the insurance company that it is medically necessary. My husband also wears a continous glucose monitor which we convinced our insurance company to cover. It has made a big change in my husbands ability to know a low or high is on it's way and to compensate adequately for it. Kudos to Maria and NBC for putting Diabetes where it belongs - front and center - WE NEED A CURE!!!!
Most people are unaware of the unique needs of women with diabetes.  For example, hormones present their own challenge in treating diabetes through the life stages- puberty, pregnancy, menopause, etc.  I encourage ALL women with diabetes to visit DiabetesSisters.  We offer a "Sisterhood" of women with diabetes with whom you can share your story, ask questions, and be heard.    We have a number of programs/services that are geared toward the specific needs of women with diabetes.  We are also working to provide positive role models (for example, with our Triathlon Team of women with T1 and T2 diabetes) because there are so few women with diabetes in the media today.  

After all, women are now living longer and therefore there are more of us around who have diabetes!  Why not come together, share our knowledge and support each other to reach our full potential!

Hope to see you/talk to you soon!    
Thanks for the great story.  I lost my mom to type 2 diabetes in 2003.  I wish they would have had the pump when she was alive. Thanks for sharing.
I'm up in Toronto, Ontario Canada, and caught part of the show today with Maria speaking about her father's life with diabetes.  I was horrified that his sugar levels are so out of control that they fear for him all the time.  That's not the way to enjoy life, but thrilled to hear that he is now on the pump.  I was 10 when I was diagnosed 32 years ago.  *Just* this past Feb I changed from the syringe to using the pens and I love it!  Much more control and I've learned so much about counting my carbs and taking a particular dosage per carb count, per meal.  Much better control and I've learned to eat healthier.  The Ontario government has just announced that they will supply the pump to adults (they've supplied it to children for a couple of years now) so I plan to move to the pump in the next couple of months.  It amazes me that there is not enough education out there (world wide) to assist all diabetics, no matter when they were diagnosed due to the changes in the medical field and advances that have happened.  Support is the main thing in order to understand how easily this disease can be managed with the right steps and medication.  I owe a major thanks to my Diabetes Education Nurse from our local hosptial who provides an education course, and support regarding diabetes including the move to the pump.
One of the greatest resources for a person with diabetes is a Certified Diabetes Educator CDE.  I am a health care professional that has dedicated over 25 years to helping individuals acquire the tools (knowledge) they need for this self managment disease. I myself am a Registered Licensed Dietitian Certified Diabetes Educator.  CDE's can be physicians, nurses, dietitians, as well as pharmacists.  You may find these specialized healthcare professionals in hospitals, private practice and retail pharmacies.  They are some of your best resources to get the facts.
Thank you, Maria!! As a mother of an 8 year old afflicted with Type 1 Diabetes I'm thrilled that you have have opened this forum to educate people. Type 1 is often misunderstood because of the medias focus on Type 2 Diabetes. In Feburary of this year she was put on the pump and yesterday to out excitment she was given the news that her A1C level is currently at it's lowest it's been in the past 3 years!! So why we continue to battle this disease with all it's up and downs we know that research is moving in the right direction. As we are preparing for our annual JDRF walk-a-thon this weekend, my daughter said to me last night that she feels and she knows their will be cure by the time she is 16.Now that is our PURPOSE in life!! Thank you again and prayers to your family.
Can anyone tell me the e-mail address of the woman on Today's show that is lighting "light bags" for awareness for type I diabetes.  My nephew was recently diagnosed (he's 3) and we are all still trying to figure out what this means.  We would love to spread awareness.  If anyone knows, please e-mail me.  h.palmer2@gmail.com  Thanks so much.

I believe there is already research being done along this line, but I highly suspect that sometime in the future, it will come out that the synthetic pesticides used in the farming industry that our food is doused with, as well as all of the chemical preservatives added to processed foods is a major contributor in the diabetes and cancer equations.
I am so glad to see the Today show being proactive in providing education regarding the detection and prevention of diabetes.  As a mother of a child with Type 1 and health care provider I found the information to be a bit confusing for the public.  A comment was stated that "diabetes can be prevented" but the clarification between Type 1 & 2 was not identified in this area--Type 1 CAN NOT be prevented.  Please consider this in the future because I feel it creates a negative image for so many afflicted with Type 1.  Thanks again for stressing the importance to educate children from an early age, I have been very active in this mission also and have seen the impact that can carry onto their adult lives.


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