@laraa.katharin: It hurt in ways I didn’t have words for back then, but it also made me strong. It forced me to grow up, to protect myself, to become my own safe place. Everything I went through happened for a reason. Every loss, every disappointment, every tear shaped me into the woman I am today. And if you’re reading this while carrying your own pain, know this: Your story doesn’t end with what hurt you. What broke you once can become the very thing that builds you. You are stronger than you think. You are allowed to heal at your own pace. And one day, you’ll look back and realize that everything you survived made you powerful. I carry my past with me, not as a weakness, but as proof of how far I’ve come — and as a reminder that healing is possible for all of us 🤍 #HealingJourney #selflovejourney #gymmotovation

Lara • Verlustangst Mentorin

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Tuesday 10 February 2026 11:01:39 GMT

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Comments

hazmira :

Told you about my father, yet you still don’t understand me

2026-03-17 08:55:31

682

xyz 🪐🌷 :

i only live because my mother need me 🙂

2026-03-19 02:14:37

331

ChayDTN :

Learning to live without you dad has been the hardest thing 😔🕊️💔

2026-03-23 15:50:42

132

maritiana :

Silent repost 😭😭

2026-03-10 22:40:48

56

✨ Teryn ✨ :

My dad recently passed away and this shit hit home like no other. I pray all you queens heal from this trauma 🥺

2026-04-01 01:55:36

12

Jules :

Ich fühls sehr!🥹 drück dich🫂

2026-02-12 22:13:09

3

Des :

Ohhh this is a sensitive subject 🫠

2026-03-31 01:20:43

8

🐆 :

2026-03-03 18:14:58

45

Hope✨ :

All I ever wanted was to have a dad and my mom to love me…

2026-03-27 01:34:20

5

𝐚𝐝𝐢𝐬𝐬 :

my biggest heartbreak, nothing can hurt me more than this

2026-04-09 23:44:48

5

Sonia :

Expect my kids, can’t live without them

2026-03-24 01:47:44

3

﮼هاني :

2026-03-18 10:16:35

4

Crystal Silva🍬 :

He was my biggest heartbreak ❤️‍🩹

2026-03-23 05:22:11

17

charrrrrxo :

Just lost my Dad at the weekend and this hit really hard ❤️‍🩹

2026-03-19 00:30:01

19

𐙚 ̊ :

2026-03-15 23:22:34

3

MaBelle :

Me too🥺

2026-03-01 20:17:35

7

L :

2026-03-17 17:31:42

3

Tink Berenzy :

cause girl 😭

2026-04-11 04:31:57

1

7f4ith :

And the last 🙏🏽.

2026-04-10 19:30:12

1

Yadira Robles :

except my kids they are the only exception 🤍 miss my dad so much 💔💔

2026-03-29 05:46:47

2

wendymoiron :

this

2026-03-23 13:45:07

2

aio559603 :

My grandpa😔

2026-04-05 16:54:05

1

Mark :

My first heartbreak was also when my dad passed away.

2026-04-18 16:32:15

1

kel :

2026-02-13 01:02:27

2

To see more videos from user @laraa.katharin, please go to the Tikwm homepage.

Other Videos

Pathological Demand Avoidance (or “Pervasive Drive for Autonomy”) is a nervous system disability. While our children often have less trouble with social communication than their non-PDA autistic peers (not always, but I believe most of the time), and “may have friends, make eye contact and talk,” they are often viewed as being too “high functioning” for systematic and structural care. I remember trying to get in-home caregiving support and we were told our son wasn’t “severe enough.” Yet minute-to-minute it was difficult to keep my two children physically safe in the home because of the extreme fight-flight behaviors, and meanwhile my son was barely eating enough calories to sustain him. Because we are privileged, we were able to make many structural and lifestyle changes to support my son: We were able to pay for in-home caregiving support using an au pair and to get a service dog on a short timeline. We pay for a private school where he receives accommodations. We pay for health insurance that allows for coverage of non-behavioral based therapies that support his nervous system. Most families do not have the luxury to set up their own private systems of care. Cumulative nervous system activation is disabling to these children and teens, and crippling to families, especially those who are lower-income, single-parent households, or from marginalized identities who frequently intersect with (and likely have fear of) child protective services and other institutional entities. This is not a YOU issue. It is not your CHILD’s issue. This is a structural issue. What I teach here does not negate these truths. Rather, it is radically accepting these current constraints (whether we like or agree with them) and then helping you find agency within them. I believe the first step to more structural support is getting PDA recognized as an official diagnosis as soon as possible. Obviously, this needs to be part of a collective effort and is also a part of our mission here at At Peace Parents.

Pathological Demand Avoidance (or “Pervasive Drive for Autonomy”) is a nervous system disability. While our children often have less trouble with social communication than their non-PDA autistic peers (not always, but I believe most of the time), and “may have friends, make eye contact and talk,” they are often viewed as being too “high functioning” for systematic and structural care. I remember trying to get in-home caregiving support and we were told our son wasn’t “severe enough.” Yet minute-to-minute it was difficult to keep my two children physically safe in the home because of the extreme fight-flight behaviors, and meanwhile my son was barely eating enough calories to sustain him. Because we are privileged, we were able to make many structural and lifestyle changes to support my son: We were able to pay for in-home caregiving support using an au pair and to get a service dog on a short timeline. We pay for a private school where he receives accommodations. We pay for health insurance that allows for coverage of non-behavioral based therapies that support his nervous system. Most families do not have the luxury to set up their own private systems of care. Cumulative nervous system activation is disabling to these children and teens, and crippling to families, especially those who are lower-income, single-parent households, or from marginalized identities who frequently intersect with (and likely have fear of) child protective services and other institutional entities. This is not a YOU issue. It is not your CHILD’s issue. This is a structural issue. What I teach here does not negate these truths. Rather, it is radically accepting these current constraints (whether we like or agree with them) and then helping you find agency within them. I believe the first step to more structural support is getting PDA recognized as an official diagnosis as soon as possible. Obviously, this needs to be part of a collective effort and is also a part of our mission here at At Peace Parents.

تصميم وتنفيذ | ˢᵃᵘᵈ𝚏𝚒𝚌𝚝𝚒𝚘𝚗 من التراث ..بـ 𝖺𝗂 على شان ما تزعل على أخوك يا مرزوق إذا خف عقله والعبت فيه شيعية تقول الهوى سني وأنا أقول يا مطفوق متى العشق فرق في قلوب الهواوية لو إنك لمحت اللي لمحته بوسط السوق تمنيت شوفة كربلا كل عصريّة #شعر #الحان #اغاني #تصميم #مشاعر

تصميم وتنفيذ | ˢᵃᵘᵈ𝚏𝚒𝚌𝚝𝚒𝚘𝚗 من التراث ..بـ 𝖺𝗂 على شان ما تزعل على أخوك يا مرزوق إذا خف عقله والعبت فيه شيعية تقول الهوى سني وأنا أقول يا مطفوق متى العشق فرق في قلوب الهواوية لو إنك لمحت اللي لمحته بوسط السوق تمنيت شوفة كربلا كل عصريّة #شعر #الحان #اغاني #تصميم #مشاعر

Grandma want to roast Zara🤣🤣#creatorsearchinsights #ai #trend

Grandma want to roast Zara🤣🤣#creatorsearchinsights #ai #trend

#актор #рек #приколи #кавер #котики

#актор #рек #приколи #кавер #котики

Drêw..🙂!

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