Guilt

I agree. But, to get the A1C lower, she needs to modify her diet, dosage, and exercise routine.

That is why I mentioned Dr Bernstein.

The hormone checks for testosterone, cortisol, and thyroid are very important and should be checked as well.
If cortisol is high then insulin requirements will be high and metabolism can be low.

Testosterone, even for females, plays an important role. All diabetics have a deficiency to some degree, as this is a part of the disease.

No type 1 should have an A1C that high. If the only problem is insulin vs carbs, a pump can fix this very easily.
I know a type 1 in his early 40’s that has an A1C of 4.3 .
He uses a pump, and watches what he eats, and exercises daily.

The easiest way to control A1C is to drink loads of water all the time. The law of dilution will dictate that the lower the concentration of glucose in the blood, the lower the A1C will be.

Protein and fat will yield the lowest blood sugar spikes. Interestingly enough, eating protein and fat, then using NPH, the curves are nearly identical.

Lowering basal blood sugars with say Lantus or Levemir will also yield better A1C’s. But no matter who you are, you must exercise to get the glucose out of your blood by means of raising your metabolism.

Once a person determines how to adjust their blood sugars the right way ( AKA Paleo Diet, insulin, and exercise ), the rest is just going to be of habit.

Of course females have their own set of blood sugar problems due to hormonal cycles, but this too can be accounted for.

My wife and son both tend to ignore my injection time. They tend to overlook it like I am doing something very normal. Which I am.

They do not love me any less. When I wasn’t taking insulin, my 8 year old son used to feel sad that I wouldn’t eat any french fries he offered to share. That hurt me more than it did him, but eventually he understood.

Most of my life is about the same as it was before diabetes. It’s just a little something extra I have to deal with.

Please note: you got diabetes through no fault of your own, unless you self inflicted it, which isn’t likely.

My only brother is severely mentally disabled. He’s 35 years old and has the overall abilities of a 3 year old. He doesn’t speak or read, can’t comprehend complex directions, doesn’t dress himself, rarely uses the bathroom himself (and has his share of accidents), and has a mild seizure disorder. He is very uncoordinated and often breaks things, either by accident or as a simple result of childish behavior. He communicates by grunts, hand gestures, facial expressions, laughs and cries. He sometimes eats things that are toxic, and has had multiple stomach surgeries. He lives in a residence for adults like him, at a cost shared by my parents and the state. He requires constant supervision. By any dictionary definition, he is indeed a “burden”.

My only brother is the most emotional person I know. He expresses joy in the most jubilant way possible, laughing and pulling people together in group hugs. He appreciates the simple things in life: a funny slapstick moment on TV, a dog licking his hand, a visit from his brother. His smile makes everybody around him smile, his laugh makes everyone else laugh. He has a very endearing personality. When something upsets him, the rest of us feel bad because he can’t comprehend what just happened or why. My life can be so stressful, yet I’ve learned to essentially live vicariously through him and simply enjoy the moments through the eyes of someone who doesn’t comprehend anything more.

I don’t know why Daniel is the way he is, but I do know that he is the reason so many other people are the way we are. We are a bit more sympathetic to those who can’t help themselves, a bit more appreciative of the good things around us, a bit more tolerant of those who are less able.

When I was younger, I dreamed of the day when he could somehow be “normal” and I could have a sibling to talk to and play with like all of my other friends did. Today, I know that won’t happen, but I couldn’t imagine Daniel being anyone other than who he is, He has meant so much to me, to my parents, my grandparents, my aunts and uncles, and my cousins, and has shaped our lives and beliefs for the better. Is he difficult to handle? Of course. Would I be absolutely devastated if something happened to him? Absolutely.

My point is this, Sagwabetes: in our day-to-day lives, we tend to only look at our day-to-day needs - what we ask of ourselves and what we ask of others. We tend to lose sight of the larger picture, how important we are to others and how we, unknowingly, help others. But people need us, rely on us, love us. I’ve been diabetic for 30 years, and I’ve sometimes felt like the “burden” you speak of. But I’ve seen the other side as well, with my brother. People don’t necessarily contribute to society by the inventions they create or the money they raise. The most important contributions can be simply by the interactions we have with others, and the lessons and thoughts that those other people walk away with.

It took a lot of courage for you to write this post, and your four sentences are more powerful than my long ramblings of meandering thoughts. But I hope it helps you to believe that you are not a burden, and you are not a useless waste of space. Unless you are a pure evil-doer (which I’m sure you’re not, those types have reached international infamy), you mean something to somebody. Your living with diabetes has inspired somebody. Your expressions of guilt have come as companionship to someone else who feels the same way, and feels alone. You’ve been open and honest, and inspired others to be the same.

We need you here. Please understand this.

Scott, what a beautiful & heartfelt post. Thank you for sharing your kind words & kind heart.

Please hang in there Sagwabetes. You are not alone in these feelings. Diabetes can be overwhelming, and can be a constant grind. I went through these same emotions you describe 2 years ago. I ended up in the hospital for 3 days because I didn’t know how to ask for help. After that I got into group therapy, saw a therapist and a psychiatrist one on one. I was able to turn my life around and get healthy again.

Remember these feelings will pass. Continue to reach out and ask for help. Things will get better if you take these small steps. My thoughts are with you!

Sagwabetes, one of the most valuable lessons diabetes taught me is that it’s really okay to ask for help.

When someone needs your help, does it make you feel useful, purposeful? I bet you have folks you’d drop everything to help when they need it – and you have the power to give someone that gift.

PM me if you want to share more.

Thank you Gerri. As I wrote it, I was feeling bad that I was making the post too much about myself, but it goes to show that people are needed in more ways than they sometimes recognize!

I should add one more thing, back to the original theme of the post. When the decision was made by my parents to put my brother in full-time residential care, rather than live at home with us – that was the biggest feeling of guilt any of us had ever felt. I was about 12 years old at the time (he was 10) and was feeling confused and a bit betrayed by my parents “sending him away”. Imagine that. With all of his special needs, WE were the ones feeling guilty, not him! It all works out in the end, though. He comes home (my parent’s house, his second home) every other Friday and stays until Sunday. Still very much a part of our lives.

Scott…you have answered this so well…and have touched all of us deeply with your wisdom and discernmemt. Thank you.

Scott, could not have put it better my self! Any kind of long term problem can and will make us stronger people, more able to empathise than if we did not have this condition. I have to just laugh at mine! And sometimes just think, “What the hell?” throw my little wobbly in the form of some forbidden food, and then get right back and deal with it!

Big group hug for Scott!

That must have been incredibly hard. I can’t even imagine.

Thanks everyone for your kind words, but really – this isn’t about me. This is about self-worth, which as Bikette eloquently put it, is “truly relative”. We touch so many other lives through our very existence, whether in person or online. As a result, these people form opinions and beliefs, and then pass them on to others. I’ve adjusted my behaviors and beliefs at times because of the way I see strangers interact (parent/child, customer/clerk, and so on- sometimes positively and sometimes negatively). They don’t even know that I saw them or took lessons away, but it helps me to be a better parent, a better husband, and an overall better person. I am sure that someone will then see me, finds a lesson in that, and pass it on – all unintentionally. The way our actions affect others compounds dramatically in ways we can’t even understand.

By telling my story, I would hope that Daniel has now made others feel better about themselves, more appreciative of life, and more accepting of others. He will never know the impact my telling will have. In all likeliness, neither will I.

I’m not a religious person, and I don’t subscribe to the belief that God put so-and-so on this earth for a reason. But I do believe that we all contribute to society in one way or another, and we just need to be willing to open up our eyes, our hearts, and are minds. We all teach, learn, and contribute in our own way.


Hi Sagwabetes…me again!

Just popping in to see how you’re doing. You were heavy on my mind last night as I lay in bed. You know, we all have something. Call them conditions, concerns, issues, quirks, glitches, disorders or whatever. None of us are perfect. NONE.

Some of the conditions are invisible to others, but very much still there for the person who has it. (Something like the wind…no one can see it, but it’s still there and we can experience its presence).

So it is with us, we are all placed here for a purpose. We all touch someone directly or indirectly. You touch us and others, and we/others touch you. It may be a long term relationship, or a brief encounter…no matter. It may be a word said, or a smile. Sometimes a mere presence is enough.

It’s unfortunate that one has diabetes, with or without complications…or epilepsy, or asthma, or severe allergies, or cancer, or cystic fibrosis, or downs syndrome, or countless other conditions, BUT we all impact someone’s life, whether we want to or are aware of it or not. Us yours, and yours ours. That’s why I come to Tudiabetes. I know you have touched MY life :heart:

If they love you, just think how bad they would feel if you weren’t with them. Hang in. Things will get better. I had this feeling for a while, recently, and things got a lot better. Now that it is Summer, your body will probably feel better and more lively! Just breathe and live on the inside, not the outside(: <3

Now Linda. You are a bit wrong there. I am perfect. I am a perfect dummy! LOL

The biggest problem I see is that if people cannot actually see a problem, they say you don’t have a problem.

Tsk, tsk. Shame on them.

I know a few people like that. They see me as usual. but underneath lies a diabetic, struggling to find a way to live with the disease and still have some semblance of a life.


WOW! I just reas Scot’s post now I’m crying. What he said.

How are yo today?

I do not have diabetes; both my children do. So, from the point of view of someone who, YOU feel, would be be burdened: I tell you to please don’t feel that way. The world would be a very sad place without those two extraordinarily brave young men, my life would be so empty without them. Diabetes is now part of them, me and that is the way it is. Guilt should not even be part of the love equation. Love is unconditional, forever and never a burden.
Take care of yourself, maintain the best control you can, have a great life for you and for the people you love so that love lives on for a really, really long time. We need a lot of love in this crazy world.

thank you … there’s no more i can say

thank you. i’m still hanging in for now…