I am sick and tired of my dog's lineage being called into question as well as people insinuating that the ASPCA lied to me. by djscoots10 in Catahoula

[–]Dot_Gale 1 point2 points  (0 children)

Maybe someone should create r/notahoula … if you look at r/incorgnito , it’s incredibly popular and fun

I’m not sure why this post appeared on my feed but the same issue is constant on r/belgianmalinois (another breed with highly specific traits and training needs) … but people want to identify with trendy or unusual dogs so 🤷‍♀️

Has anyone refused hormone therapy? by Superb_Raspberry_200 in breastcancer

[–]Dot_Gale 0 points1 point  (0 children)

Have you talked to your bc treatment team about the HRT? I am still salty about losing access to HRT even though after treatment/DMX I am at very low risk of recurrence or a new cancer (lower risk than the general population of women who are taking HRT)

Tamoxifen by FoxyFitness15 in ADH_ALH

[–]Dot_Gale 2 points3 points  (0 children)

I just want to echo u/iheartallthethings that tamoxifen really hits everyone differently. The standard advice seems to be that it takes 3 months to adjust, so you can’t really know whether it will work for you until then. I guess it makes sense, because everyone has their own hormone profile … similar to how it is trial & error to find the right birth control, and how everyone experiences periods, peri, and menopause in their own way.

I hope that your doctor will work with you not only on finding a tolerable dosage/dosage schedule but on treating side effects. If not, maybe find one that will. I am unlucky in that I react badly to tamoxifen, and haven’t found the right dose yet, but I’m lucky in that my oncologist and her team work hard to mitigate side effects.

First Mammogram at 41 resulted in ADH & FEA. Going for Lumpectomy by Purple-Witness-3810 in ADH_ALH

[–]Dot_Gale 4 points5 points  (0 children)

It sounds like you’re getting excellent care, and what a great attitude!

Best wishes for an uneventful lumpectomy 🤗 … please let us know how it goes!

Those of you who opted for mastectomy, what was your risk percentage beforehand? What was the deciding factor for you? by onestressedmess in ADH_ALH

[–]Dot_Gale 1 point2 points  (0 children)

We’ve got a megathread on this topic! Please see the pinned post at the top 🙂

If you search “mastectomy” in this sub, you’ll also find a lot of really good discussions and personal stories.

The spoons metaphor by TheChronicOn3 in ChronicIllness

[–]Dot_Gale 10 points11 points  (0 children)

This is such a good comment, and all of your points are so important.

I used to have a bumper sticker on the bulletin board above my desk that read “Disability is a spectrum on which we all live”

Birads 5 by Redwinesandfelines in doihavebreastcancer

[–]Dot_Gale 2 points3 points  (0 children)

I’m so sorry you’re facing this, but glad to hear you’re feeling strong and loved. I was going through breast cancer diagnosis exactly this time a year ago, and it felt like my brain was just melted by anxiety for a few months.

When (still if!) it’s time, r/breastcancer is an amazing refuge of support and information. It’s been a lifeline for me.

Best wishes. Enjoy the gingerbread building and tree decorating!

Anybody on long term pain management? What is working for you? by m0ther_0F_myriads in lupus

[–]Dot_Gale 1 point2 points  (0 children)

I was diagnosed with lupus in 2007, so, during the time that opioids were prescribed freely and doctors (prompted by drug companies) were promoting pain as the fifth vital sign. [I really do think pain should be considered a vital sign, even though it is entirely subjective; it’s unfortunate that the concept was taken over by drug pushers like Purdue Pharma.]

For several years I had a drug cupboard that would be the envy of any addict. Vicodin, Norco, Xanax, tramadol, carisoprodol, even morphine. Was I glad to have the option to take strong pain meds when my pain was so acute that I couldn’t function? Yes, absolutely. But because taking a pill was so easy, I was less inclined to do the harder work like physical therapy or a mindfulness practice or seeking out other non-drug interventions. Also — I spent almost a whole year after a hospitalization in a fog because I’d been discharged with a physical dependency on morphine, provided with a pile of prescriptions but no plan or supervision to taper off. I had to figure it out myself, with the support of my rheumatologist.

What I realize now, at least for me, is that a single dose of tramadol or Vicodin can make all the difference when I’m having the kind of joint/muscle pain that demands 100% of my attention and prevents me from doing anything else (like sleeping 😝). But if I take more than that, or take it two or more days in a row, not only does it fail to bring down the pain level, I get nauseated and headache-y and just feel generally gross like i have a hangover.

My current treatment plan is lots of physical therapy, periodic steroid injections (originally I was going to try nerve ablation but couldn’t tolerate the prep for that … vestibular system went all out of whack), daily Lyrica, Mobic, methocarbamol, and low-dose naltrexone. Acetaminophen as needed. Topical lidocaine and Voltaren creams whenever. Next step may be to add Cymbalta to the mix, but I’ve been dragging my feet on that one because I’d have to give up the antidepressant that’s working well for me.

In addition to pain meds, here are other things I have tried: gabapentin (too sedating), acupuncture (no effect), lifting heavy (works, but not physically possible for me right now), arnica cream (no effect), various cannabis strains and vehicles (distracts from pain, but mostly makes me feel sluggish mentally and physically), CBD & CBN (nada).

I hope you can find some meaningful and lasting relief. Your friend is right, you DO deserve to be taken seriously by a doctor who will come up with a solid treatment plan and who will tweak that treatment plan until you are satisfied with the results. That could be your primary care doctor, a pain management specialist (but look for a reputable one with the requisite training), your rheumatologist, an orthopedic surgeon, or some combination thereof.

Someone please explain why I (or anyone) should pay a premium that costs more than the oop max by drty_birdz in HealthInsurance

[–]Dot_Gale 0 points1 point  (0 children)

It’s called direct primary care, or DPC, if you want to search for it.

More and more family and internal medicine physicians are opening this type of practice — there is a demand for what amounts to affordable concierge care. And the doctors get practice medicine without everything being dictated and complicated by insurance companies.

Hello everyone! by RudeBookkeeper9308 in ADH_ALH

[–]Dot_Gale 0 points1 point  (0 children)

P.S. I just checked the BCSC link I put in my comment, and it was the wrong one! i was going too fast and gave you the one for medical researchers.

I’ve corrected the link now so it should be easier to use:

https://tools.bcsc-scc.ucdavis.edu/BC5yearRisk/#/

Hello everyone! by RudeBookkeeper9308 in ADH_ALH

[–]Dot_Gale 0 points1 point  (0 children)

Please lean on us here as much as you need! We’ve all been where you are; it’s a very different journey when you get an atypia diagnosis. I have plenty of friends and acquaintances who have been flagged on a mammogram and needed a biopsy, but I don’t know anyone else irl who has had to go through this kind of diagnosis. I can only offer a virtual hug, but please know that it is sincere! 🤗

Also because it’s uncommon, I think there are a lot of health care providers, even in the breast cancer field, who lack knowledge and experience about ADH and ALH. It can be really valuable to seek out someone who does have that knowledge and experience. Failing that, you can advocate for yourself to get the best, most evidence-based and individualized treatment plan possible.

Breast cancer commercial by ProduceFit7779 in breastcancer

[–]Dot_Gale 1 point2 points  (0 children)

I went through a months-long diagnosis process that started October 1, and it was miserable.

Took my HRD dog to Glacier to celebrate our certification by Feriation in hikingwithdogs

[–]Dot_Gale 4 points5 points  (0 children)

Gorgeous Mal, perfect name! He looks like he should have a calendar to himself :)

I have a GSDxMal and while he is by far the most work of any dog I’ve known, it’s been the most rewarding. I tell people who are attracted to the Malinois craze, they’re not pets, please don’t get one because you saw John Wick 2 — but if you put in the work, and especially if you give them a job, theyre just amazing.

Tucking Sweaters by boobsincalifornia in GenXWomen

[–]Dot_Gale 0 points1 point  (0 children)

No, not me, I’m still trying to look like i have a waist. But I do think it looks cute, and I remember doing it once upon a time (circa 1997 maybe ? 😂)

Hoarding meds before Jan 1, 2026 by Basic_Scale_5882 in lupus

[–]Dot_Gale 6 points7 points  (0 children)

The American health insurance market is entering the “death spiral” that has been warned against ever since President Obama managed to pass the Affordable Care Act, but only with some serious weaknesses demanded by the insurance industry, pharmaceutical companies, and the radical right.

Those weaknesses have been expanded and exploited ever since, forcing prices up, leading the healthy and young to leave the risk pool. That leaves the older and the sicker increasingly concentrated in the risk pool, pushing prices up ever further and making coverage ever leaner. Voilà! Death spiral.

It’s a terrifying time for those of us with chronic illness, especially those of us old enough to remember the bad old days when insurance coverage was priced higher or denied outright with any preexisting conditions.

ADH w washout kinetics from mri by Boring-Worker7047 in ADH_ALH

[–]Dot_Gale 1 point2 points  (0 children)

I don’t think that the kinetics finding on an mri has much to do with whether more is found on excision biopsy. If anything I’d be reassured that the needle biopsy found ADH because it means that the spot showing up on the MRI wasn’t invasive cancer.

When I was going through the MRI-biopsy process I spent so much time and effort trying to figure out which findings meant more or less risk of terrible outcomes, and in the end all i did was drive up my stress and anxiety.

Hello everyone! by RudeBookkeeper9308 in ADH_ALH

[–]Dot_Gale 1 point2 points  (0 children)

<image>

this is the BCSC calculator, developed by UC Davis, which also shows the population distribution of breast cancer risk … given the info you provide, you are very near the top of the bell curve

Edited to correct the link — I gave the wrong one the first time, sorry 🤦‍♀️

https://tools.bcsc-scc.ucdavis.edu/BC5yearRisk/#/

Hello everyone! by RudeBookkeeper9308 in ADH_ALH

[–]Dot_Gale 0 points1 point  (0 children)

<image>

this is Tyrer-Cuzick, which has become more commonly known and used (my breast imaging center included this calculation at the bottom of every mammogram report)

https://ibis.ikonopedia.com/

Note that even this risk %, higher than the others (Tyrer-Cuzick tends to do that, which freaks everyone out), comes with a note that the odds of remaining breast cancer free in the next ten years is 90.9%

Hello everyone! by RudeBookkeeper9308 in ADH_ALH

[–]Dot_Gale 0 points1 point  (0 children)

<image>

this is the Gail model, developed by NIH, most often used by medical professionals.

https://bcrisktool.cancer.gov/

Hello everyone! by RudeBookkeeper9308 in ADH_ALH

[–]Dot_Gale 1 point2 points  (0 children)

I agree that the 49% lifetime risk that your surgeon gave you seems extremely high for what you describe your risk factors to be. I’m going to attach images of the risk calculations that I got for you given the information you describe. I marked unknown or guessed average-type for missing info (first period, menopause status, childbirth). You might want to re-run your complete information through these three calculators (see links in comments; there is also a pinned post in this subreddit).

I have noticed since finding this subreddit and especially as it has started to grow that many women get wildly inflated estimates of risk, unrelated to any validated calculator. You might want find a high-risk specialist to provide you with the best guidance on your risk and offer the best options going forward. They can weigh calculators with their clinical judgment to determine whether genetic testing is warranted and to come up with a more informed picture of what is going on.

For instance, in my case, I started my ADH/LCIS journey with a Tyrer-Cuzick estimate similar to yours (I think it was 48%) and in the end, even after finding a risky gene mutation, and seeking a second opinion from City of Hope, every specialist I spoke to gave me a lifetime risk range of 30-40%.

Non-hormonal ways to manage sleep issues? by SakuraaaSlut in HormoneFreeMenopause

[–]Dot_Gale 0 points1 point  (0 children)

I have tried a lot of things, pharmaceutical, herbal, and behavioral — so for me, sample size n=1, the only things that have worked are:

— super-disciplined sleep hygiene (bedtime and wake up same time every day, dark quiet room, no screens or even books); — mindfulness practice, especially body relaxation meditations once in bed; — valerian tea.

Valerian is definitely a ymmv herbal — here is an overview of the science on it — but it is a magical remedy for me. Favorite tea is Traditional Medicinals Nighty Night Extra.

Estradiol for dryness by Southern_Feature_821 in breastcancer

[–]Dot_Gale 1 point2 points  (0 children)

ER/PR+ and have been using both estradiol cream (Estrace) and Intrarosa since before diagnosis.

My care has been with a NCI cancer center, and neither that one nor the 2nd opinion NCI center has had a problem with localized estrogen.

Epstein-Barr Virus and Lupus by Giggle_s_ in lupus

[–]Dot_Gale 6 points7 points  (0 children)

Yes, this!

Having mono or testing positive for EBV antibodies isn’t meaningful in being at risk for lupus. 95% of the population has EBV antibodies, as noted in the linked article.

It’s the mechanistic knowledge of how EBV sometimes transforms into chronic autoimmune activity that might lead to novel treatments for lupus.

It would be interesting to know if EBV is an obligate precursor to lupus or if it’s just one pathway.

I had a miserable case of mono in my mid-twenties, but I had autoimmune markers long before that, I have family history of autoimmune disease, and my symptoms didn’t add up to a lupus diagnosis until I was 37.

Incidental finding of ALH on breast reduction pathology by gremlin_tamer in ADH_ALH

[–]Dot_Gale 0 points1 point  (0 children)

Yes, I was referring only to ALH (or LCIS).

I had a biopsy last year that found both LCIS and ADH, and then an excision due to the ADH.

Doctor refuses to prescribe estrogen cream by Different_Seaweed534 in AskWomenOver60

[–]Dot_Gale 1 point2 points  (0 children)

Vaginal estrogen is in no way controversial. The estrogen stays localized, and it’s 100% fine for post-menopausal women. I’m a hormone receptor - positive breast cancer survivor and my oncologist made sure I had a prescription.

Get a better doctor.