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Vaginal dryness: nonhormonal options and how to evaluate benefits

Vaginal dryness: nonhormonal options and how to evaluate benefits

I didn’t set out to write a safety plan. I stumbled into the idea after a rough week when my thoughts felt like weather—stormy one hour, oddly calm the next. Willpower kept letting me down, and I kept assuming “future me” would be stronger. That wasn’t fair to future me. So I decided to build something steadier: a simple, portable plan I could reach for when my mind was noisy and my memory unreliable. The surprising part was how human it felt—less like a rulebook and more like a note from a kinder version of myself that said, “Here, do this first.”

What follows is the exact way I put that plan together and how I organized essential contacts so they’re never more than a tap or a wallet card away. It’s practical, it’s honest, and it doesn’t promise miracles. It just gives the next right step when that’s all I can handle. If you’re reading this for yourself or for someone you love, I hope it offers a little structure and a lot of compassion.

The moment I realized a plan beats willpower

The shift happened when I admitted that crisis thinking is different from calm thinking. In the calm zone, I know my values, the people who care about me, and the tools that work. In the crisis zone, those same truths can feel far away. A safety plan is basically a bridge between those two zones—written in my clear moments, designed to be followed in my cloudy ones.

  • High-value takeaway: Write the plan when you’re steady, so it’s there when you’re not.
  • Keep it short, specific, and action-led—no pep talks, just steps.
  • Expect to revise it. My first draft was wordy; later versions became more like a recipe card.

When I started, I skimmed a few credible overviews to learn what clinicians actually mean by “safety planning.” One plain-English message stood out: most plans follow a simple sequence that moves from internal coping to people to professionals to environmental safety. If you like a starter map, you can glance at resources like the CDC’s suicide prevention pages, the NIMH overview on warning signs and supports, the Suicide & Crisis Lifeline (dial or text 988 in the U.S.), and practical handouts from clinician groups.

A six-part map that stays with me

I built my plan around six parts. I keep each part to two or three bullets because in tough moments I don’t want options; I want the next breadcrumb.

  • 1) My warning signs — I write the earliest signals I tend to ignore: “scrolling in bed all morning,” “canceling plans without rescheduling,” “brittle sarcasm,” “thinking in all-or-nothing.” When I see two or more, I move to step 2.
  • 2) Internal coping strategies — Things I can do without telling anyone. I list three only:
    • Five-minute sensory reset: cold water on wrists, open a window, feel the air.
    • Set a 10-minute timer and walk outside, no phone.
    • “Name 5–4–3–2–1”: five things I see, four I feel, three I hear, two I smell, one I taste.
  • 3) Social distractions — People and places that are low-stakes. Examples:
    • Text J. “Are you free for a quick coffee?”
    • Public place with people around: bookstore, grocery store, church foyer.
  • 4) Supportive contacts — A short list of people I trust with the truth, not just a distraction. My list includes a sibling, a friend who “gets it,” and one person who can help make calls if needed. I include exact words to send: “I’m having a hard time and could use company or a check-in call.”
  • 5) Professional help — I write the names and numbers I am most likely to use:
  • 6) Making my space safer — I choose one or two immediate actions that reduce risk:
    • Have a trusted person hold onto items I shouldn’t access when distressed.
    • Lock up or limit quantities of medications; use a timed pill organizer.
    • Remove reminders or notes that fuel rumination; replace with my plan card.

That’s the skeleton. I keep the full plan on a single printed page and a mirrored note on my phone. When I update it, I write the date in the corner so I know it’s current.

Turning names into a lifeline directory

Knowing whom to call matters, but finding the number fast matters more. I turned my contacts into three tiers and made each tier absurdly easy to reach.

  • Tier A: Always-call list — 2–3 people who have said “call me, no questions.” I add them as favorites in my phone and star their texts. I also write their numbers on my wallet card in ink.
  • Tier B: Good-enough supports — 3–5 people I can text for company or a distraction. Their numbers live in a dedicated “Support Circle” group chat so I don’t have to choose when my brain is tired.
  • Tier C: Professional safety net — clinician(s), local urgent care/ER, and the 24/7 U.S. lifeline at 988. I also keep links to reputable organizations for education and sober second thoughts, like the CDC and NIMH.

For each person or service, I include:

  • Best method — call, text, or both
  • Availability — “nights are best,” “weekdays only,” “anytime”
  • What to say — a one-sentence script, so I don’t overthink it

Practical touches that helped:

  • ICE and Medical ID — On iPhone, I set up Medical ID so emergency contacts are visible from the lock screen. On Android, I added “Emergency information” with contacts that can be viewed without unlocking. That way responders can find help even if I can’t speak.
  • Speed dial — I placed 988 and my top person on the first row of my phone’s home screen.
  • Wallet card — A simple index card with warning signs, top 3 coping steps, and Tier A numbers. I taped a duplicate inside a kitchen cabinet.

Words to use when words are hard

I used to get stuck typing and deleting. Now I keep a few scripts that lower the barrier to asking for help. Copy, paste, and tune as needed:

  • To a close friend: “I’m having a tough mental health moment and could use company by phone or text. No need to fix anything—could you stay with me for a bit?”
  • To a support contact: “I’m practicing my safety plan. Can we talk for 10 minutes or swap messages while I do a short walk?”
  • To a clinician or clinic: “I need an urgent check-in about suicidal thoughts. What’s the soonest appointment or the best place to go now?”
  • To myself, on the card: “Do step 2 now. If that fails, call Tier A. If no answer, call 988.”

Little habits I’m testing in real life

I treat my plan like a living document. I try things, keep what helps, and retire what doesn’t. A few habits earned a permanent spot:

  • Micro-routines for mornings — I stack a 2-minute stretch with opening the blinds and drinking water before touching my phone. It sounds small; it reduces early ruminating for me.
  • Grounding kit by the door — headphones, a soothing playlist, a smooth stone, mint gum, and a spare printout of my plan.
  • Check-in Fridays — I message my support circle: “Green, yellow, or red this week?” It normalizes updates when I’m okay, so asking for help later feels less awkward.
  • Means safety as a routine — I refill meds weekly and store extras out of sight; the key to a lockbox lives with a trusted person. I review this setup after any tough week to keep it honest.

If you like evidence-informed guides, I found it useful to read summaries from national health organizations and clinician groups. They echo the same theme: make it specific, accessible, and practiced. Even the best plan loses power if it lives in a forgotten app folder, so I practice step 2 on calm days—literally walking through the first coping action for five minutes to make it muscle memory.

How I capture the plan on paper and phone

My rule: if I can’t find my plan in five seconds, I redesign where it lives.

  • Paper — One page, large font. Top half is steps 1–3. Bottom half is contacts and safety changes. I print two copies and date them.
  • Phone — A pinned note named “SAFETY PLAN” and a photo of my paper plan saved as a favorite. I also attach contact cards to the note so I can tap-to-call.
  • Home screen — A folder called “Calm” with my plan, a timer app, a maps shortcut to the nearest open public place, and 988 dialer shortcut.

I also built a tiny checklist I can tick off in minutes:

  • Notice two warning signs
  • Do one internal strategy
  • Text one person from Tier B
  • Call one person from Tier A or 988 if needed
  • Change one thing in my environment

Signals that tell me to slow down and ask for help

Plans are steadying, but they’re not magic. A few signs tell me to move quickly toward people and professionals:

  • Thoughts feel specific and urgent — If I catch myself planning or collecting items, I stop and call 988 or a local emergency number. This is not a time to self-assess alone.
  • Isolation increases — If I’m avoiding everyone for a day or more, I break the streak by going to a public place or calling my Tier A person.
  • Substance use ramps up — I remove access and ask someone to be with me. If needed, I go to urgent care or an ER to get stabilized.

If you’re in the U.S., you can dial or text 988 for the Suicide & Crisis Lifeline. If you may be in immediate danger, call 911 or go to the nearest emergency room. If you’re outside the U.S., your local health ministry or a World Health Organization page can point to country-specific supports.

What I’m keeping and what I’m letting go

What I keep:

  • Specificity — “Walk outside for 10 minutes” beats “get fresh air.”
  • Practice — I rehearse steps when I’m calm so they’re ready when I’m not.
  • Redundancy — Paper + phone + friend who knows my plan.

What I’m letting go:

  • Perfectionism — The plan doesn’t need perfect words; it needs to be findable.
  • Shame — Asking for help is the skill. Every time I do it, I build that muscle.
  • Going it alone — Crisis is not a test of character. It’s a health moment; I treat it like one.

Quick reference links to save

FAQ

1) Do I need to make this plan with a professional?
You can start on your own and refine it with a clinician if you have one. Professionals can help tailor steps, troubleshoot barriers, and coordinate care if risks rise.

2) How often should I update a safety plan?
I review mine after any challenging week and at least every three months. Update contact info, remove steps that you don’t use, and add what reliably helps.

3) What if I don’t want to worry my family?
Choose people who respond in the style you need. It’s okay if your Tier A contacts are friends or peers rather than relatives. You can also practice asking for help in calm times so the first ask isn’t during a crisis.

4) What if I’m supporting someone else?
Ask how they want to be helped in advance. Offer to hold a copy of their plan, store a lockbox key if that’s part of means safety, and agree on words that mean “I need help now.” Keep lifeline numbers handy and know the closest urgent care/ER.

5) How do I handle access to medications or other risky items?
Use the least complicated safe option that actually works in your life: locked storage, smaller fills, or temporarily transferring items to a trusted person. If you’re unsure, talk with a clinician about practical ways to reduce risk while keeping your routine workable.

Sources & References

This blog is a personal journal and for general information only. It is not a substitute for professional medical advice, diagnosis, or treatment, and it does not create a doctor–patient relationship. Always seek the advice of a licensed clinician for questions about your health. If you may be experiencing an emergency, call your local emergency number immediately (e.g., 911 [US], 119).