I am a Type 1 Diabetic Warrior

Conquering life living with Type 1 Diabetes

Saturday, December 6, 2025

Hormones and my hair loss journey

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Type 1 diabetes is complicated and exhausting to manage. It becomes even more challenging when you’re a woman dealing with constantly fluctuating hormones. Hormonal shifts directly affect insulin sensitivity, and trying to balance the two can feel like an impossible task.

For some reason, many people believe that once you’ve lived with Type 1 long enough, it becomes easy—that you simply “figure it out” and coast through life. I’m not sure why that misconception exists, but I truly wish the general public understood Type 1 diabetes better. Most people don’t take an interest in a disease unless they or someone they love is battling it, and that lack of understanding can feel very isolating.

For several years, I’ve felt that something was off hormonally. Not long ago, if you told a general practitioner or nurse practitioner that you suspected hormone imbalance or wanted to explore hormone replacement therapy (HRT), they often dismissed you. If you weren’t in full menopause, they acted like you were imagining things. Thankfully, the recent HRT movement has opened doors for women in perimenopause and menopause to finally be heard and supported.

My own HRT journey started in March of this year. I began with progesterone, then added testosterone cream. I don’t remember the exact month, but I do remember my hair starting to fall out. Later, I saw another doctor about adding estrogen, and once I started it, the hair loss increased dramatically. I eventually asked my nurse practitioner for oral minoxidil, which can push hair follicles through the shedding phase into growth. Unfortunately, the combination of everything—plus what was probably a naturally timed shed cycle—caused me to lose nearly half my hair.

I stopped all HRT and minoxidil and started taking a DHT-blocker supplement I found on Amazon. Within a month, the hair loss completely stopped. The next month, I restarted HRT. I paused it in September and resumed again in November, and now I’m experiencing the most dramatic regrowth I’ve ever seen. I have my normal hair length—and underneath it, what looks like a two- to three-inch buzz cut growing in everywhere. It’s wild, but I’m so grateful it’s coming back.

If you’re struggling with hormonal hair loss, this is the supplement I use and love:

(Using Subscribe & Save can also knock a percentage off, depending on how many subscriptions you have.)

Beyond the hair journey, HRT has been life-changing for me. My arthritis and back pain have almost entirely disappeared. I’m sleeping better than I have since I was a teenager. I have more energy, can work out harder and longer, and I’m seeing strength gains I haven’t seen in nearly 20 years.

I’m so grateful to finally feel like myself again.


How Hormones Can Increase DHT and Cause Hair Loss

Hormones play a huge role in how our bodies function, and that includes how our hair grows. One hormone in particular—DHT (dihydrotestosterone)—can have a major impact on hair health.

DHT is made when your body converts testosterone into a stronger form using an enzyme called 5-alpha reductase. Everyone has DHT (women included), but problems start when hormone levels shift and the body begins producing too much of it.

Here’s how it leads to hair loss:

Hormonal changes—including menstrual cycles, postpartum shifts, perimenopause, PCOS, or even stress-related hormone fluctuations—can increase the activity of 5-alpha reductase.

When that enzyme becomes more active, more testosterone converts into DHT.

Excess DHT shrinks the hair follicles, making the strands grow thinner and weaker over time.

Eventually, the follicles can become so small that they stop producing hair altogether.


This process is known as androgenic hair loss, and it’s extremely common. The frustrating part is that it’s not about “doing something wrong”—it’s a hormonal response your body creates on its own.

Understanding how DHT works can help you explore the right treatments, whether that’s reducing inflammation, supporting hormone balance, or using products that block DHT production at the follicle.

Tuesday, October 28, 2025

Hair loss and peri menopause

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Im back to my blog!! Super long hiatus and a ton of life changes.  I needed to share this product with you all, it's saved a little bit of my sanity through this life transition.  I will post more soon about everything. 

For those of you who have ventured into peri menopause or menopause and have started HRT like I have, the hair loss is real!

I lost half my hair and so I freaked out and stopped taking it.  I went on this supplement from Amazon, the hair loss stopped and my hair is growing back.  I started taking this then went back on HRT including testosterone and my hair is still growing, not shedding! 

Monday, April 18, 2022

How incredibly dangerous the stomach flu can be with t1d.

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I have sat and thought about this blog post over and over while writing it in my head without putting it into actual text many times. I don't want to come across as ungrateful for my knowledge of type 1 diabetes (aka t1d) or ungrateful that my child has a disease she can, God willing, live a long lifetime with.  I do, however, feel it is necessary to share just how dangerous a stomach/gastrointestinal virus can be with t1d.  

My little warrior had a crazy day, which I blogged about on April 8th.  Well unbeknownst to me she was coming down the the stomach virus/flu as we all tend to call it.  She woke up at 430am on Saturday, actually made it downstairs and puked.  Then puked a few more times.  Then her blood sugar started falling.  After lots of crying and begging her to eat some smarties, just like glucose tablets, she ate a few and her blood sugar came up a bit.  Incredibly scary moments.

Friday, April 8, 2022

Honeymoon phase

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My little warrior's pancreas is working overtime lately.  She has had only basal insulin all day, not a single bolus.  Honeymoon phase is insane and insanely frustrating! The other day her pump site somehow managed to get near a blood vessel, which I had no idea about until her bolus sent her crashing into the 50's then of course her dinner hit full force since the insulin was in and out so fast so then she shot to the 300's.  I love insulin pumps except for when crap like that happens.  I only knew that was the issue after pulling the site the next day and the cannula was full of blood.  Go figure.  Somedays I really feel like pulling all my hair out and just crying until my tears dry up but I know that won't accomplish a damn thing.  So I pull myself out of it and say this is just another day in the life of type 1 diabetes=just do the best you can do for today and tomorrow is a new day, start fresh.  After years of managing my own type 1 diabetes and now my little kid's diabetes I am not sure how I will have any sanity left by the time she moves out some day....then my worry will shift to worrying about her because she is not in my care anymore.  For the love of God PLEASE someone cure type 1 Diabetes before my baby moves out.   I wish there was a way to navigate the honeymoon phase but there is not and there is no way to even know or guess what it is going to do. I wish this disease was easier to manage and not like a total crap shoot most days.

Wednesday, March 30, 2022

Fitbit Versa 3 mechanical issue

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I have had my Fitbit Versa 3 since November 2020.  It broke last night with a known issue.  I contacted Fitbit via their lovely chat feature within the app and told them the side button had stopped working.  They told me this issue is not something that can be fixed with troubleshooting.  Ah, it's a known mechanical failure of this watch.  I'm out of their warranty period by 4 months. My $200.00 watch was only good for 16 months.  Awesome.  So they sent me a measly discount via my email to buy a new one.  So glad I'm a loyal fitbit user.  For whatever reason I bought the Square Trade warranty when I got the watch, it was 45.00 and Square Trade deductible was 30.00...so I'm not really sure it was worth it but a new Versa 3 is now down to 179.00 go figure. So now I will wait for my watch to arrive so I can continue to be able to monitor my blood sugar and most importantly my little warrior's blood sugar with the ease of looking at my wrist and have it vibrate when she or I go above or below the limits I have set up. 

Tuesday, March 8, 2022

Insulin price cap and links to help you get your insulin.

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"US pharmaceutical companies and insulin manufacturers react to proposed legislation that would cap insulin costs and prevent significant rises in the costs of prescription drugs."


"Here’s more information on how to get insulin at lower cost:

Sunday, March 6, 2022

Diabetes stigma and how hurtful it can be.

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When I was on insulin shots I faced a lot of really horrible comments, horrible looks and I even once got turned into h.r. for taking a shot in the break room at a really crappy job I had.  They actually suggested I take my shot in the dirty germ infested bathroom!! Seriously.  Assholes. 

What have you had to deal with when taking your insulin shots?  

I have been on an insulin pump now for almost 13 years out of the 21 years I have had type 1 diabetes. I do not ever plan on going back to shots and all of the terrible comments, stares, looks of complete disgust and how much my staying alive was ruining their lives. Their lives.

I'm incredibly grateful for pump technology and now having my little girl on a pump because I really needed to spare her from some of the ugly sides of living with a life long incurable disease as much as I could. She still hates having the pump attached to her nonstop but she is enjoying not needing 10-15 shots a day, there is a lot of snacking when you never stop moving and burning your energy off, and now being able to go back to her normal ability to eat when she is hungry and not have to debate it for another damn shot.  I'm not sorry for saying insulin shots suck royally.  A pump is so much better, more accurate and easier to adjust and not live with the never ending lows from long acting insulin.  I seriously despise long acting insulin.

Don't stare at a person giving themselves an insulin shot, don't say shitty mean comments, put yourself in their shoes- look at the world thru their eyes.  It sucks, it's hard, we hate it...don't make this shit any harder than it needs to be.  Most of us know what we are up against, don't need the hey you can go blind or go into kidney failure or lose a leg or foot thing....yeah....do not need to hear that shit one more time. Seriously.  Especially not about how diabetes killed your family member...that is not helpful ever in any situation.  We know, we have also lost loved ones to this disease and it scares the crap out of us. 

Having my little girl get diagnosed with this damned disease had really ticked me off, made me angry again, lit a fire under me and makes me want to protect her from all the hurt that she has to deal with.  I can deal with this for myself but for her it kills me to my core, smashed my heart and reignited all the pain and suffering I went thru in the beginning. I don't know how to navigate this ship but I'm trying my best and I want to change the way people feel entitled to comment on other people's diseases or conditions in negative ways.  


Tuesday, February 22, 2022

Im feeling beat down

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#Diabetes #Dexcom #TandemDiabetes #Type1Diabetes #dsma

 I try so hard not to let Diabetes beat me down or make me feel like I am losing control but this week has been really hard, like crushing my heart hard.  I know having my little warrior on an insulin pump will give her the best life and best possible outcome for longevity with type 1 but holy crap it is hard.  She has cried every day about how much she hates Diabetes, hates having the pump attached to her and hates the way the site feels.  It is such a huge adjustment and really huge when you are little. 

I remember adjusting to the pump was hard for me and pump sites always hurt but I could cope with it because I was an adult.  Every time she cries I swear my heart breaks a little bit more for her but I put on my brave mom face and try to let her know it will be ok and she will get use to it, even though it is bullshit she has to get use to it.  

Why don't we have a cure for this disease yet! Every time someone says something insensitive I try hard to brush it off but man it is like a dagger to my heart because I hate this shit too.  All the harsh things people say start to add up.  They all compile in my brain and I know someday they will crush her too.  Diabetes isn't unlike any other disease and I don't understand why people feel like they can say horrible things to the people living with it. 

Type 1 Diabetes sucks enough as it is without people making comments about how they could NEVER do it or NEVER wear a pump, NEVER take a shot, NEVER be able to count carbs, NEVER be able to poke their finger, NEVER this or that or the other.  NEVER is NOT AN OPTION!  You do it or you DIE.  

Let that sink in, you do it or you die, there is no other option, no choices, no vacations, no breaks ever. Me and my little warrior will be diabetic for the rest of our lives and we will fight the complications and blood sugars every single day.  To add the bullshit people say on top of it is just too much.  Tell people they are brave, strong, courageous and that they are doing a great job living with Diabetes and that if you had Diabetes yourself, you would hope to do as good of a job living with it.  

I have never once ever heard anyone say the mean terrible things they do about Diabetes for any other disease.  I have never once seen a meme or joke about any other disease online other than Diabetes.  I have never heard anyone joke about getting Cancer, MS, Parkinsons or any other disease, but yet people joke about Diabetes and how doing this or that will give them Diabetes.  Its just not funny and its confusing as hell to little kids living with this shit.    

Stop joking about DIABETES, its not funny EVER and it sure the hell isn't FUN to live with.

Monday, February 21, 2022

Tandem Control IQ Alarm Fatigue

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@TandemDiabetesCare #tandem Guys/gals at Tandem for the love of GOD can you PLEASE PLEASE PLEASE let us be able to turn off CONTROL IQ ALARMS?!?!?! They are literally keeping all of us awake way too often and too much at night.  I have to set all my alarms to vibrate other than CGM alarms so I can get some sleep but the damn vibrations for control iq still wake me up and many of us up and we are GOING INSANE!  I am literally nearing shutting control iq off at night just to get some sleep! 

My little warrior is on an insulin pump

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My little warrior's insulin pump went on Friday.  Everything from my perspective went well but how on Earth do I help her accept the feeling of an infusion set and the level of discomfort it brings along with it?  She is thin like me so I am always aware of my site and sometimes they hurt no matter what, but as an adult I can cope with it.  This is the 2nd most stressful part of having your child plus yourself have type 1 diabetes.  The first was most definitely diagnosis and giving her multiple daily shots.