Start / Confessions of a Rare Disease Mama / Coffee catchup

Coffee & catchup

26 min • 15 augusti 2023

Whew! The past few months have been BUSY. I'm going to catch you guys all up on this episode. As always, thanks for joining me on this wild ride. Happy listening, friends!

Resources & Links for this episode:

Buy Soaring Together: Amazon, Barnes & Noble, or locally at Bike Trail Books in Loveland and the Cincinnati Zoo Gift Shop
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- TikTok: @rare_mama
- Facebook: Jillian Arnold & Confessions of a Rare Disease Mama
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Senaste avsnitt

BONUS EP: What to do when the world feels like too much

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Life Lately: Solo Parenting, Sick Kids, & School Plans

28 maj | 30 min

Creative Fundraising in the Rare Disease Community – Global Genes Panel Recording

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Life Lately: A Rare Mama Catch-Up

23 april | 32 min

Navigating Resources and Grants with Advocacy Abby

5 mars | 59 min

Real Food Blended Diets Made Simple: A Conversation with Registered Dietitian Hilarie Geurink

29 januari | 62 min

A Mother’s Legacy: Lauren Williams’ Commitment to GRIN1 Families in Honor of Her Son

17 januari | 53 min

Goals for 2025, Tackling Winter Blues, and SNOWMAGEDDON

7 januari | 23 min

A Rare Mama’s Reflections on the Holiday Season with Yours Truly

22 december 2024 | 33 min

Turning Pain into Purpose: Rare Mama, Ashley Haywood’s Advocacy for Sanfilippo Syndrome

3 december 2024 | 67 min

Special Family Transitions with Special Needs Divorce Coach, Mary Ann Hughes

5 november 2024 | 41 min

Mini Ep: My EXCITING, BIG Announcement!

1 oktober 2024 | 16 min

The Eight Different Types of Advocacy with Director of Community Engagement of Global Genes, Daniel DeFabio

17 september 2024 | 59 min

Officially entering my self love era

3 september 2024 | 29 min

Prioritizing your mental health as a caregiver with Founder and Executive Director of We Are Brave Together, Jessica Patay

20 augusti 2024 | 59 min

Our MAW Disney trip recap with special guest (& my better half), Don Arnold

1 juli 2024 | 42 min

Mini solo episode: If I could go back in time

4 juni 2024 | 17 min

Mission: Inclusion with Speech Language Pathologist & inclusive children's book author, Megan Craft

21 maj 2024 | 48 min

Turning grief and trauma into growth and healing with Past Life Regression Therapist, Alena Gourley

26 december 2023 | 61 min

Catchup/ dealing with the holiday blues

2 december 2023 | 21 min

How to fundraise like a BOSS with special guest and fellow rare mama, Brittany Markham

31 oktober 2023 | 83 min

Life Update

23 oktober 2023 | 26 min

When the "FOMO" starts creeping in as a medical parent

6 oktober 2023 | 24 min

Is my child's diagnosis a "karmic wake up call" from the universe?

3 september 2023 | 25 min

Coffee & catchup

15 augusti 2023 | 26 min

My top travel tips for road tripping with your medically complex child

14 juli 2023 | 24 min

Ain't no shame in my anti-depressant game

30 juni 2023 | 28 min

A Father's Perspective with Rare Disease Dad & Director of Community Engagement for Global Genes, Mr. Daniel DeFabio

12 juni 2023 | 55 min

Top lessons I have learned in my first four years of being a rare disease parent

30 maj 2023 | 38 min

How to best support the caregiver parent in your life

16 maj 2023 | 33 min

Where I have been the past two months

3 maj 2023 | 34 min

How to find and manage the right care team for your medically complex child

14 februari 2023 | 31 min

Career transitions and life as a rare disease mom to twins with Angel Aid Cares Operations Manager, Megan Loden

31 januari 2023 | 65 min

The word(s) I will live by in 2023

17 januari 2023 | 31 min

Cheers to a new year! Our top moments of 2022

3 januari 2023 | 33 min

Walking through that pesky tunnel of grief

23 december 2022 | 19 min

How to fit in some fun during the busy month of December

13 december 2022 | 23 min

Family planning after a diagnosis with special guest and fellow rare mama, Taylor Sabky

6 december 2022 | 69 min

A COVID-style Thanksgiving

29 november 2022 | 23 min

Learning when to let go of control (or as my Grandma always said, "que sera sera!")

22 november 2022 | 21 min

Stepping out of survival mode and putting your best self forward with special guest: podcast host and life coach, Lauren Lowery

15 november 2022 | 51 min

'Tis the season for colds and flus

8 november 2022 | 31 min

Our BIG news

25 oktober 2022 | 25 min

Making the leap into a healthier lifestyle with Nutrition Coach and Personal Trainer, Sabrina Miller

18 oktober 2022 | 54 min

Celebrating every inch-stone!

11 oktober 2022 | 25 min

One family, two different rare diagnosis' with special guest (and a TRUE rare disease warrior mom) Nadia Slatch

4 oktober 2022 | 65 min

Stream of consciousness/ Roman turns FOUR

27 september 2022 | 19 min

Reminiscing about our big Florida trip with special guest: my husband, (and car-packer extraordinaire) Don Arnold

20 september 2022 | 30 min

Life update/stream of consciousness and how I'm learning to let grief & joy co-exist

13 september 2022 | 30 min

Best in class caregiving with mejo app founder Ryan Sheedy

6 september 2022 | 52 min

BONUS EPISODE How to deal with ignorant comments

3 augusti 2022 | 18 min

We made it to the double digits! Life update + Special Announcement

22 juli 2022 | 19 min

Life Update/Stream of consciousness

12 juli 2022 | 31 min

The 5 minute journaling techniques I use to help declutter my brain

5 juli 2022 | 22 min

How to (kindly) cut ties with a therapist or doctor who is no longer serving your child in the way they need

28 juni 2022 | 29 min

How to make connections and utilize all your resources as a rare disease parent

20 juni 2022 | 30 min

Father's Day Episode with extra special guest: my husband (AKA: Dadvocate-EXTRAORDINAIRE)

14 juni 2022 | 38 min

How to continue to nurture your relationship with your spouse as a special needs parent

6 juni 2022 | 29 min

Trusting your "parental instincts"

30 maj 2022 | 34 min

The post-holiday funk

30 maj 2022 | 34 min

Our diagnosis journey

19 maj 2022 | 29 min

Coffee & catchup

Senaste avsnitt

BONUS EP: What to do when the world feels like too much

Life Lately: Solo Parenting, Sick Kids, & School Plans

Creative Fundraising in the Rare Disease Community – Global Genes Panel Recording

Life Lately: A Rare Mama Catch-Up

Navigating Resources and Grants with Advocacy Abby

Real Food Blended Diets Made Simple: A Conversation with Registered Dietitian Hilarie Geurink

A Mother’s Legacy: Lauren Williams’ Commitment to GRIN1 Families in Honor of Her Son

Goals for 2025, Tackling Winter Blues, and SNOWMAGEDDON

A Rare Mama’s Reflections on the Holiday Season with Yours Truly

Turning Pain into Purpose: Rare Mama, Ashley Haywood’s Advocacy for Sanfilippo Syndrome

Special Family Transitions with Special Needs Divorce Coach, Mary Ann Hughes

Mini Ep: My EXCITING, BIG Announcement!

The Eight Different Types of Advocacy with Director of Community Engagement of Global Genes, Daniel DeFabio

Officially entering my self love era

Prioritizing your mental health as a caregiver with Founder and Executive Director of We Are Brave Together, Jessica Patay

Our MAW Disney trip recap with special guest (& my better half), Don Arnold

Mini solo episode: If I could go back in time

Mission: Inclusion with Speech Language Pathologist & inclusive children's book author, Megan Craft

How to get through a long hospital stay & my inpatient must-haves

All things TRAVEL with Accessible Adventures Founder, Kristy Cook

My inner debate on a third child and what I have come to realize

Talking about all the things with The Rare Life's Madeline Cheney

Turning grief and trauma into growth and healing with Past Life Regression Therapist, Alena Gourley

Catchup/ dealing with the holiday blues

How to fundraise like a BOSS with special guest and fellow rare mama, Brittany Markham

Life Update

When the "FOMO" starts creeping in as a medical parent

Is my child's diagnosis a "karmic wake up call" from the universe?

Coffee & catchup

My top travel tips for road tripping with your medically complex child

Ain't no shame in my anti-depressant game

A Father's Perspective with Rare Disease Dad & Director of Community Engagement for Global Genes, Mr. Daniel DeFabio

Top lessons I have learned in my first four years of being a rare disease parent

How to best support the caregiver parent in your life

Where I have been the past two months

How to find and manage the right care team for your medically complex child

Career transitions and life as a rare disease mom to twins with Angel Aid Cares Operations Manager, Megan Loden

The word(s) I will live by in 2023

Cheers to a new year! Our top moments of 2022

Walking through that pesky tunnel of grief

How to fit in some fun during the busy month of December

Family planning after a diagnosis with special guest and fellow rare mama, Taylor Sabky

A COVID-style Thanksgiving

Learning when to let go of control (or as my Grandma always said, "que sera sera!")

Stepping out of survival mode and putting your best self forward with special guest: podcast host and life coach, Lauren Lowery

'Tis the season for colds and flus

Our BIG news

Making the leap into a healthier lifestyle with Nutrition Coach and Personal Trainer, Sabrina Miller

Celebrating every inch-stone!

One family, two different rare diagnosis' with special guest (and a TRUE rare disease warrior mom) Nadia Slatch

Stream of consciousness/ Roman turns FOUR

Reminiscing about our big Florida trip with special guest: my husband, (and car-packer extraordinaire) Don Arnold

Life update/stream of consciousness and how I'm learning to let grief & joy co-exist

Best in class caregiving with mejo app founder Ryan Sheedy

*BONUS EPISODE* How to deal with ignorant comments

We made it to the double digits! Life update + Special Announcement

Life Update/Stream of consciousness

The 5 minute journaling techniques I use to help declutter my brain

How to (kindly) cut ties with a therapist or doctor who is no longer serving your child in the way they need

How to make connections and utilize all your resources as a rare disease parent

Father's Day Episode with extra special guest: my husband (AKA: Dadvocate-EXTRAORDINAIRE)

How to continue to nurture your relationship with your spouse as a special needs parent

Trusting your "parental instincts"

The post-holiday funk

Our diagnosis journey

BONUS EPISODE How to deal with ignorant comments