So my angst and anger and annoyance aside, (that's a lot of 'a' words), I have a boyfriend, and he loves me immensely. He knew at the beginning of our relationship that I was a type one diabetic; our relationship actually started because I was diagnosed with it. But lately my moods have been horrid, I don't want to check or deal with the type one, etc. He tries to get me to check or take my insulin and I just get mad at him. He keeps eating chocolate or three or four servings a sitting of mashed potatoes or whatever else of high carbs. He doesn't seem to understand how much this bothers me. He also eats most of my serving, which bothers me too. But as much as I try to tell him how it makes me feel, it doesn't help him understand and he just gets defensive. He drinks soda late at night. I feel like we are always at eachother. He doesn't believe me when I say mood swings can be caused by diabetes; he thinks I can just do some deep breathing and it will go away. Since the type one onset, I have been diagnosed with a rare form of eczema, bipolar, depression, anxiety, eating disorders, anger (my shrink wanted to admit me to a mental hospital for evaluation). I was also just told I have a thyroid issue which affects my calming down after getting mad near impossible to do. I had just ended an abusive relationship after the diagnosis. I am a full time college student (made the dean's list the last three semesters). Just some background. But what has made me write this is that I was just telling him about the artificial pancreas system, and he said it had been out for years. I told him it is still going through its trial phase and he wouldn't believe me even after I showed him proof. I feel like he thinks I'm incompetent. Out of the two of us, I figure I would know if there were new developments because I have the disease. It has consumed me mentally. I get emails hourly about type one/diabetes. I constantly worry about my levels even though I dont check. Plus the eczema has made it difficult enough to check my fingers.

I'm at a loss about what to do or how to get through to him. I hate the fighting but I can't get a grip, which like I said, he doesn't believe.

Tags: college, diabetes, help, one, student, type

Views: 618

Reply to This

Replies to This Discussion

The only answer to worrying about your levels is to check. How ever much you know, your boyfriend may be correct to think that you're "incompetent" if you don't test.

Without checking, neither of you can fix any potential problems. Re the AP, you should give him points, even if he was 'wrong' for knowing about what *is* out, a CGM and pump, which is pretty close to an artificial pancreas and can do a pretty decent job. But you have to test, as I think you have to do with an AP too.

Re the food, maybe mashed potatoes aren't the best solution (not to mention they're not the best for anyone, D or not, they are one of my favorites though, a highlight of knocking my teeth out in a bike wreck a couple of years ago was eating them for a few days waiting for the new teeth...) but they aren't impossible but you have to test, bolus, eat and test again, just like pretty much anything else you'd eat. There's no way around that. If you're eating lower carb, that can be a big help but I've found it useful to count 53% (ok, I round to 50% most of the time...) of protein and bolus for that too.

Re the overall situation, I think that in order to prove how smart you are, you should test enough to manage your diabetes. That will prove how smart you are to anyone more than knowing about an artificial pancreas vs. various other options that are out there. One final thing about recent problems would be to suggest that maybe the honeymoon is over? The diabetes one, not the boyfriend! It's usually a year or so out and dx in March, listed on your page, suggests that it may be going on, in which case a doctor might determine that and adjust your plan based on reported high BG. If you haven't been to your endo recently, perhaps it would be good to approach them with that?

I take 15 units of long lasting every night, and then I am supposed to be at a 1:10 insulin to carb ratio, but I am so scared of going low, I usually don't take the quick acting unless I ate a lot. But thank you, I have three appointments next week, so maybe something will be changed..

I understand that at least a part of your mind is always on diabetes. I think almost all diabetics feel this way, weather they are well controlled or not. The fact is that if you want to have a long healthy life your best chances involve testing. You need the data from testing in order to make educated decisions on food and insulin. I really think you need to test more and always take insulin when you are ingesting carbs. Also understand that he is nagging you because he loves you and wants you to be healthy. While I understand that this can be annoying, you should also understand that he is just trying to help you. If checking on your fingers is too problematic, then you may want to consider alternate site testing:

I have never been that upset about others loading up on carbs, candy, etc. in front of me. It is his choice to eat it just like it is your choice to eat some or not. I don't think you need to worry about his eating behaviour, its his choice. If it makes you hungry watching him eat, then I would suggest that you find a low carb food that you can eat while he is eating it or leave the area.

The issue isn't so much what he's eating, it's more how much he's eating because now I am paranoid about anyone I love getting type two. My mother, when I got diagnosed, kept eating to try and get type two; I wanted to slap some sense into her. It's just ridiculous. But I do need to check more. The other thing is now that I don't want to go high with my levels, I don't want to eat. It's a vicious cycle. Thank you.

This doesn't help the problem with your boyfriend, but I have had eczema for 40 years, since dx and beginning to eat low carb I have found that my hands are not so tender with rashes. I rather suspect it could be wheat, but whatever it may help if you do eat low carb for a bit and use the cream the dr. gives you when ecxema is bad. I hope you will discover that eating low carb will help with at least one of your problems. Maureen

They couldn't even figure out what it was. Two cultures, three visits to the ER, and seven top dermotologists later, they said it was eczema. Now I have to take pills and use steriod creams, no matter what my levels are. It's just another thing in the list of 'not-wanting-to-deal-with'. But alright, thanks so much for the advice!

We all have a long list of must learn how to deal with them and achieve your goals (BE HAPPY) . Try not to lump all of your issues together and just take one day at a time and deal with what needs to get done on that day, worry about tomorrow, tomorrow.

Don't worry about what none PWD's eat, just take care of your needs first and then you can help others around you. I'm sure you have flown on a commercial airplane, they always say if the cabin has a loss of pressure put your mask on first and then help others and small children around you , take this to heart, this is how life works. Your spirit must be strong or you cannot help or deal with others around you.

No one is ever going to understand how you really feel...really....;-) cut your family and friends some slack, if they do not have Type1 diabetes they are clueless and are probably just making fumbling attempts to show some said it...they love you....

I always think about the "Bete's" I even dream about it....that's the norm for something "chronic" in our life.

Remember the Bete's is your cross to carry and it's not anyone's business but yours, only you need the knowledge to control your BG, and you can choose who you share your feelings with, it may not be a good idea to share all of your feelings about Bete's with your boyfriend he may not be able to handle all of your stress...a local support group may be better.

The only way you can gain knowledge about your BG is to test and document the outcome...test, test, test.


Have a great New Year...:-)


Thank you for your thoughts. Truly. The airplane thing makes complete sense.. I have been testing more the last few days, which doesn't help if I don't stay on that. Thank you; I am slowly making a list of everything that needs to be accomplished each day. Slowly but surely..

Unfortunately he will never truly get it unless he becomes diabetic himself. I believe it is asking a lot to expect a non D person to understand when he hasn't experienced it. I do believe that he understands that he loves you and wants to be part of your life. I think he understands that to be with a healthy and happy you he must help you, you would do the same for him I'm sure. His attempts at help may be annoying but they come from a good heart. Helping our loved ones is just something we do in a relationship.

I think there is more going on here than his annoying attempts at help. The stress and depression that is so often associated with D can adversly effect relationships. An understanding partner can go a long way but we must also look to ourselves to overcome it.

Thanks so much. I'm trying to not snap as much, but it is just so difficult. If I keep my levels level, I still feel like it doesn't work as much as I would hope.

You know, the frustration works both ways. When my relatives see books in the checkout called "Cure your diabetes in 14 days!" and "Reversing Diabetes" with pictures of docs on the cover at the checkout, they wonder why I'm such a slacker. I've had it 30+ years, yet I'm so lazy that I'd take insulin and check my bg all the time instead of cure myself. What a slacker! I got chewed out by my father in law just last week. He can't believe that I'm so lazy.

And how about those artificial pancreases, why don't we just go buy one at CVS? They're sitting on the shelves in plain view.

Above written all tongue in cheek of course. (Well, OK, I did get chewed out by my father in law for being so lazy that I haven't cured myself yet.) A lot of my relatives don't know the difference between a pump, a bg meter, and a vial of insulin. It is EXTREMELY common for them to assume that my bg meter delivers insulin. Was EXTREMELY common 20+ years ago too.

It's crazy how much people don't know and think they know. The costs for such things are through the roof; I had to argue with my school for my health insurance through the state because they figured I could pay $300+ a month for my prescriptions. My boyfriend at least is trying to learn, we just hit heads so much with this.. He knows how to give me my shots, check my blood, and how much of my levemir to give.




From the Diabetes Hands Foundation blog...

DHF Joins Diabetes Advocacy Alliance

Diabetes Hands Foundation is incredibly honored to join the Diabetes Advocacy Alliance, an organization with the drive and potential to affect a powerful, positive impact on diabetes and healthcare policy. Diabetes Advocacy Alliance is a 20-member coalition of leading professional Read on! →

Helmsley Charitable Trust Renews Support for DHF

HELMSLEY CHARITABLE TRUST GRANTS SUPPORT TO DIABETES HANDS FOUNDATION FOR FOURTH YEAR  Funding in 2015 to support major transitions in programs and leadership at Diabetes Hands Foundation BERKELEY, CA: February 18, 2015 – The Leona M. and Harry B. Helmsley Read on! →

Diabetes Hands Foundation Team


Melissa Lee
(Interim Executive Director, Editor, has type 1)

Manny Hernandez
(Co-Founder, has LADA)

Emily Coles (Head of Communities, has type 1)

Mila Ferrer
(EsTuDiabetes Community Manager, mother of a child with type 1)

Mike Lawson
(Head of Experience, has type 1)

Corinna Cornejo
(Director of Operations and Development, has type 2)

Desiree Johnson  (Administrative and Programs Assistant, has type 1)


Lead Administrator

Brian (bsc) (has type 2)


Lorraine (mother of type 1)
Marie B (has type 1)

DanP (has Type 1)

Gary (has type 2)

David (has type 2)


LIKE us on Facebook

Spread the word


This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information: verify here.

© 2015   A community of people touched by diabetes, run by the Diabetes Hands Foundation.

Badges  |  Contact Us  |  Terms of Service