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Sweet Speakable Sorrow

the cultivation of spiritual complaint

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#52 My ALS Journey—The Electronic Dilemma
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#52 My ALS Journey—The Electronic Dilemma

February 15, 2025February 15, 2025

  It’s a good reminder here that my mother rarely asked for help. She was highly independent, and even throughout her diagnosis, I was called to come to […]

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#51 My ALS Journey—Rule 15: Be a Crusader & Know Your Disease
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#51 My ALS Journey—Rule 15: Be a Crusader & Know Your Disease

February 15, 2025February 15, 2025

Almost every post I add to this blog guts me. Of course, I miss my mother, but I am also overwhelmed with the sweet gifts her life continues […]

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#53 My ALS Journey—My Anniversary Date
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#53 My ALS Journey—My Anniversary Date

February 15, 2025February 15, 2025

“Lady, that’s where Jasper is. He’s in the green house over there!” I’m driving with my just six-year-old granddaughter, Selena, and I strain to turn my head to […]

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#50 My ALS Journey—Well Deserved Tantrum
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#50 My ALS Journey—Well Deserved Tantrum

January 11, 2025February 15, 2025

I am very sorry indeed to hear that anxieties again assail you. (By the way, don’t ‘weep inwardly’ and get a sore throat. If you must weep, weep: […]

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#49 My ALS Journey—Yesterday vs. Today
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#49 My ALS Journey—Yesterday vs. Today

February 14, 2024November 26, 2024

This week, I came across a new website entitled Her ALS Story. The site “seeks to raise awareness that ALS impacts young women diagnosed before 35 and provide […]

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#48 My ALS Journey—The Rule Book: Rule 12
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#48 My ALS Journey—The Rule Book: Rule 12

January 27, 2024January 11, 2025

A Rule Book by Susan Catlett Rule #12 for ALS This Rule is a reminder: it is not all about me. This is a tough rule because my […]

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#47 My ALS Journey—The Rule Book: Rule 11
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#47 My ALS Journey—The Rule Book: Rule 11

January 27, 2024January 11, 2025

A Rule Book by Susan Catlett A huge thank you to all for your encouraging words, thoughts, and prayers; it really helps to know you are all out there. […]

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#46 My ALS Journey—The Rule Book: Rule 10
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#46 My ALS Journey—The Rule Book: Rule 10

January 17, 2024January 11, 2025

A Rule Book (cont.) Rule Book and Artwork by Susan Catlett Adding rules to my Rule Book is great fun: it allows me to think through my days, […]

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#45 My ALS Journey—The Rule Book: Rules 7, 8 and 9
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings

#45 My ALS Journey—The Rule Book: Rules 7, 8 and 9

January 15, 2024January 11, 2025

A Rule Book (cont.) Book by Susan Catlett Having fun and looking for joy in each day is one of my personal rules. I started my Rule Book to […]

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#43 My ALS Journey—Need for a Rule Book
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings

#43 My ALS Journey—Need for a Rule Book

January 1, 2024January 11, 2025

A Rule Book By Susan Catlett A Rule Book. That is what I need, something to tell me what to do and how to feel, because I don’t […]

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#42 My ALS Journey—Rude Betrayal
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings

#42 My ALS Journey—Rude Betrayal

January 1, 2024January 11, 2025

Rudely, my body continues to betray me. Rudely, my body betrays me and fatigues me before I am ready. Last night, we were at my daughter’s, having dinner […]

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#41 My ALS Journey—Being Stupid
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#41 My ALS Journey—Being Stupid

December 27, 2023January 11, 2025

“The attempt to develop a sense of humor and to see things in a humorous light is some kind of a trick learned while mastering the art of […]

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#40 My ALS Journey—Treasured Moments
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#40 My ALS Journey—Treasured Moments

December 27, 2023January 11, 2025

“Our problems cannot always be fixed, but they can always be accepted as the very will of God for now, and that turns them into something beautiful.” Elisebeth […]

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#39 My ALS Journey—Consumed
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#39 My ALS Journey—Consumed

December 27, 2023January 11, 2025

“The world tries to silence our expression of feelings of hopelessness and despair. This “shushing” breeds shame and an overall feeling that seeking comfort is selfish. As a […]

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#38 My ALS Journey—The Path and the Box
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#38 My ALS Journey—The Path and the Box

December 26, 2023January 11, 2025

This blog of mothers made me laugh out loud, especially her discussion of sitting in the designated handicapped seating area in the church. Mother did not like Boxes. […]

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#37 My ALS Journey—A Good Week
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#37 My ALS Journey—A Good Week

December 13, 2023January 11, 2025

Before my mom was diagnosed with ALS, I would describe her to people by saying she “ran circles around my dad.” Which, actually is saying a lot because […]

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#36 My ALS Journey—Ten to Ten
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#36 My ALS Journey—Ten to Ten

December 13, 2023January 11, 2025

I’ve been considering what it means to be a strong Christian woman. It’s a loaded question in the world of faith. What does that exactly look like? Susan […]

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#35 My ALS Journey—Faith Believing
ALS / Family / Grief / Lou Gehrig's Disease / Outings / Susan's Steps

#35 My ALS Journey—Faith Believing

April 20, 2023January 11, 2025

Somedays, my faith waivers, and I don’t always (almost never, actually) understand exactly what that purpose is…other than hanging on for the ride. Susan Catlett Sometimes, accepting the […]

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#34 My ALS Journey—A Fun Night
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#34 My ALS Journey—A Fun Night

April 20, 2023January 11, 2025

I think my mom’s joy of buying new shoes for every journey is one of my great joys today. Recently, I completed my Ph.D. (this alone would have […]

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#33 My ALS Journey—Thank You ALS Association
ALS / Family / Grief / Jesus / Lou Gehrig's Disease / Outings / Susan's Steps

#33 My ALS Journey—Thank You ALS Association

April 20, 2023January 11, 2025

My mom loved the microphone and the stage. She appreciated the opportunity to educate and encourage others en masse. In this blog, she shares her speech at the […]

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"Life is unspeakably sad until you recover the lost language of lament. Then it becomes 'speakably' sad and an authentic journey into His presence begins."

Larry Crabb, quoted in A Sacred Sorrow by Michael Card

Welcome to Sweet Speakable Sorrow! If you are here, you may wonder why anyone would want to think about grief or suffering, let alone talk about it. Yet, God is a God who hears us in our sorrow and longs for us to bring our complaints to Him. Sweet Speakable Sorrow is a home where I learned, as taught to me by my mother, to appreciate and cultivate the language of sorrow and give it back to God in praise.

  • #52 My ALS Journey—The Electronic Dilemma
  • #51 My ALS Journey—Rule 15: Be a Crusader & Know Your Disease
  • #53 My ALS Journey—My Anniversary Date
  • #50 My ALS Journey—Well Deserved Tantrum
  • #49 My ALS Journey—Yesterday vs. Today

"Life is unspeakably sad until you recover the lost language of lament. Then it becomes 'speakably' sad and an authentic journey into His presence begins."

Larry Crabb, quoted in A Sacred Sorrow by Michael Card

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