Tag: kids

Navigating Life’s Uncharted Waters

by Mothersense, posted in Uncategorized

A journey through grief

Life has a way of teaching us profound lessons, often through experiences we never anticipated. As a mom who has navigated the tumultuous waters of grief after losing both parents, my beloved Uncle John, former in-laws, and numerous close friends, I’ve come to understand that while the journey is deeply personal, it is also one that connects us to each other in ways we might not always recognize. Today, I want to share my story, not as a means of seeking sympathy, but to offer a beacon of hope and understanding for those who might be walking a similar path. And grief is a very personal journey and no two paths are the same, please know you are not alone.

The Weight of Loss

Losing my parents was like losing the anchors that held my world steady. They were my guiding stars, my sources of unwavering support, and the keepers of family traditions. Their absence created a void that felt insurmountable. I remember the days following their passing as a blur of grief and disbelief, a cacophony of emotions that seemed too vast for words. And still I don’t feel like words can accurately describe the first few months after we lost my Daddy and Mom.

While still grieving my Uncle John and parents who were so much a part of our daily lives; we also experienced the loss of close friends, and my former in-laws. It all seemed too much, like another wave crashing against my already fragile heart. Each person’s departure brought with it its own kind of pain—a different shade of grief, yet part of a larger tapestry of loss. These were people who had walked with me through various chapters of my life, sharing laughter, tears, and countless memories. Their absence was a reminder of the impermanence of life and the unpredictability of our journeys.

Finding Strength in Vulnerability

Grief is often portrayed as a linear process, but in reality, it’s more like a swirling dance with no clear steps. At first, I sought to shield myself from the raw pain, to put on a brave face for my children and keep life as normal as possible. But eventually, I realized that embracing my vulnerability was not a sign of weakness but a source of strength. Allowing myself to grieve openly meant accepting that my feelings were valid and that it was okay to not have all the answers.

Being honest with my children about our losses was one of the hardest yet most liberating things I did. We talked about their grandparents, uncles, and my friends in ways that honored their memories while allowing us to express our sadness. It became a shared experience, one that, while painful, also brought us closer. Through these conversations, I learned that grief does not need to be a solitary journey; it can be something that unites us.

Creating New Traditions

One of the most healing things for me has been creating new traditions that honor those I’ve lost. It started with small gestures—lighting a candle in their memory on significant dates, creating bouquets for their graves, sharing stories about them during family gatherings, and visiting places that held special significance. Over time, these traditions have evolved into a way of keeping their spirit alive, blending their memory into our everyday lives. As I have one daughter planning a wedding, she will be certain to honor her grandparents and perhaps even her honorary aunt Audra in her upcoming wedding ceremony. This is how we move on. We are forever altered by the loss, but we keep the memories in our hearts, so our loved ones are ever present.

As a family, we began to find joy in creating new memories while still cherishing the old ones. We celebrated our milestones with an appreciation for the past and a renewed hope for the future. One daughter’s graduation was especially poignant, her aunt brought a rose for each grandparent who was missing. It was a way of acknowledging that while the pain of loss is profound, it does not have to overshadow the beauty of living. We celebrated and had a party and there were smiles and laughter and it was good. 

Embracing the Journey Forward

Grief is a lifelong companion, but it doesn’t have to define us. It’s a part of my story, but it’s not the whole story. I’ve learned that healing doesn’t mean forgetting, but rather finding a new way to live with the love and memories of those who have passed. It means allowing myself to experience joy again and to continue moving forward with a heart that has been forever touched by those who are no longer here.

 I recently watched the episode of NCIS where “Ducky” passed away, and although he was old and it was his time, the loss still hurt. Director Vance shared a piece of wisdom with the team that Dr. Mallard had shared with Vance upon his wife’s death, We each die two deaths, one where our body gives out and the other when our stories stop being shared. Profound words to share with those experiencing loss. Don’t stop sharing the stories. It keeps them alive in our memories and even though their physical presence is gone, they do not have to be. 

In my journey, I’ve found solace in connecting with others who have experienced similar losses. It’s through these shared experiences that we find understanding and support. We each have our own paths, but the connections we forge with others who have walked similar roads can be profoundly comforting.

A Message of Hope

If you are navigating the challenging waters of grief, know that you are not alone. Your feelings are valid, and your journey is uniquely yours. Embrace the love and memories of those you’ve lost while allowing yourself the grace to live and find joy again. Grief may change you, but it doesn’t have to diminish your capacity to love and find happiness.

In the end, life’s greatest gift is our ability to love deeply and to be loved in return. Even in the face of loss, the bonds we create and the memories we cherish become a source of strength. As a mom who has felt the weight of grief, I hold onto this truth: that the love we share with those who have left us continues to guide and uplift us through every step of our journey.

In loving memory of so many I have lost over the years, but especially:

Sandi Rene Marbut July 1993

Ila Kilcrease July 1987

John Henry Eaves June 2019

Sharena Kay Lovett May 2020

Rufus Oran Kilcrease October 2020

Emeline Marie Kilcrease November 2020

Deborah Kay Nelson April 2023

Garry Paul Roeber May 2023

Audra Marie Talley March 2024

Marcey Elaine Riley May 2024

Personally yours – Personal Development goals/obstacles

by Mothersense, posted in Messy Life

2015-07-25 14.19.05When one is trying to grow personally and develop a plan for a business there are some obstacles that will inevitably come up and perhaps slow the progress. I have taken my hubs disability as a sign that maybe we all needed to slow down and work on things as a couple, a family, and rethink where our priorities are. We seem to constantly be re-evaluating what is most urgent to deal with because we are in a lengthy “crisis” mode and I am trying my best to keep the kids away from that mode and absorb most of that onto myself and a little on my husband because feeling like you are “on the verge” all of the time is exhausting.
We have run into financial obstacles. I have unfortunately had to sell things, ask for help from local churches, cash in life insurance, pretty much take everything down to the bare bones of living so that we can continue to afford to live in our home and not be forced to surrender another home and move in with family. SO far we are managing alright but most recently the federal TANF program had me so dad gum irritated. I have medical documentation that my husband cannot work, he doesn’t even travel well. I have a document that the doctor signed that says my husband cannot be left alone because he is a fall risk, meaning I do not get to “get out” much of anywhere without arranging care for him. Finding appropriate and hopefully free care for him has proved challenging. Imagine my surprise when hubs actual physical presence is REQUIRED for an “orientation” despite the documentation provided by a medical professional saying that he cannot!! SO my TANF application has been denied, no opportunity for appeal and I will need to re-apply because re-applying takes less than 30 days and appeals can take up to 90 days….and this folks is our federal government at work. I am not really complaining because at least the help is there; I am just shaking my head at how bogged down the whole thing is for applicants and recipients.
Emotional obstacles and here I can only speak for myself but this journey has days that leave me so depleted I honestly cannot comprehend how I am awake and even remotely functional. I deal with ANGER, the whole “why us?” sort of thing and I don’t get it and I lash out and wonder what I did to be getting beat down like this…And then I realize that I am NEVER going to understand the reasons WHY. And I reconnect to a calmer place and shake off the anger and put on my smile and get back to the work of whatever the day has left to bring us. It sometimes happens as fast as it took you to read that, but certain days, days that have been just way too much, it may be 15 minutes or a couple of hours of just being in a mood. It isn’t really angry, or sad, or upset its just a dreadful place that I prefer not to be so I try not to stay there. I am not a pity party sort of person but that is usually how I refer to these lapses in my normal upbeat self. I also try to stay away from people when I feel like this. I tried the whole “keeping it in” and TRUST ME, It doesn’t work, at all, EVER! Instead of keeping it in I usually have 15 minutes a day that I sort of “let it all hang out” and it may be in the shower crying or outside away from everyone but the cat while I have a little alone time talking to God. Either way it heals me just a little bit and I can breathe a little easier and continue on my journey.
Scheduling obstacles are the most frustrating. It would not matter if I wrote out a minute by minute plan of every single day we would still end up with something not getting done because someone would want to take the schedule literally and someone else would be so free with it …well I guess you get the picture. Between my autistic/bipolar/adhd daughter and her other terrific siblings we have pretty hectic days with homeschool lessons, co-op days, chores (kids just love those), meals and meal plans. It is still a journey y’all and this household is a never-ending work in progress.
Love people even when you think they don’t deserve it, and be the light you want to see in the world!! = Love and light readers! always Jules

The Road goes on Forever…meet the crew

by Mothersense, posted in Uncategorized

Sept 2
Today I head into the local workforce center for some sort of orientation. It is mandatory because we have had to apply for federal assistance. I do not know if anyone knows or understands that being on federal assistance, when you come from a long line of blue collar joes, is a pride swallowing, soul sucking endeavor. Most people will “get” that you are asking for help, but when you are tasked with being THE person to do the asking and sometimes it feels as if you are pleading for help, it drains you. When your days are filled with phone calls concerning the health of at least one of your family members and fighting with insurance to cover things that so many take for granted. I am grateful that the assistance is there; however, I am not thrilled that I have to arrange for someone to come and stay with my family while I attend this orientation and then patch my husband through via phone because he doesn’t travel well and sitting in an office chair for 60-90 minutes will hurt him too badly. So today we will do orientation at the local workforce center. I have so much to be grateful for but right now I want to explain part of our current journey. A little “meet the crew” if you will.
My youngest girl, well she has horrible headaches and jaw problems. The simplest fix is for her to get orthodontic intervention that will re-align her jaw hopefully cutting down on the teeth grinding and most likely will put an end to most of her headaches. That is a simple solution and definitely less expensive, however Medicaid has stopped covering braces or orthodontic intervention unless it is deemed “medically necessary” so we had to be referred to a neurologist, then back to the primary care provider as a follow up and then a consultation with the orthodontist ALL so these 3 medical professionals can decide that braces and orthodontic treatment are medically necessary. Now mind you this is not a simple “straightening of the teeth” this is jaw re-alignment and straightening of the teeth which should reduce her TMJ symptoms, teeth grinding, and straighten her teeth. Someone explain to me why this loop of ridiculousness is necessary?? Why is her PCP and orthodontist word that fixing her jaw is “medically necessary” not good enough?? Oh and now the neurologist has referred us to 2 more specialists opthamologist and cardiologist, just to be on the safe side and ordered a slew of blood tests. ALL to get a jaw and teeth fixed. This is the logic I am dealing with on a daily basis. Trying to find some way to help my child who is in pain at least 4 days out of the week and often wakes herself from sleep because she is grinding her teeth!!
My husband is a different story entirely. Enrollment papers were not mailed out to us so we defaulted into a healthcare plan that we did not choose. We find out this error when his neurologist calls to confirm his appointment and get his insurance information. So guess what?? Yeah, that neurologist doesn’t accept this insurance!! So what looked like HOPE…that we got into a neurologist rather quickly has turned into NOPE…BTW I made that appointment for hubs at the same time in June that I made my daughter’s (her appointment was August 27). Primary care doctor wants to have cervical and head MRI done, to get a better picture. He tries 3 times and insurance denies. So he refers to neurologist hoping that as a specialist the neuro will have more luck getting tests ran. We may wind up going to a hospital and asking to be admitted for observation and testing. Honestly I feel desperate at times. Sleep deprived sitting up answering surveys, working my Younique business, blogging, researching figuring out some way to hustle up money to pay the bills.
My middle gal, I love her to pieces as she has such a terrific heart and she can be an incredible person. BUT, yeah you knew it was coming, she has an alphabet of diagnoses. NO really, PDD-NOS (aka autism spectrum disorder), BPD rapid cycling, ADHD, ODD and a couple of others but I try not to focus on the diagnoses because she is so much more than all of those letters. Oh and let us not forget she is also 14 and hormonal and teen girls WITHOUT any neurological and gastric issues are in and of themselves a handful. And my middle gal is more than a handful. She has good days that can be incredibly awesome where she sleeps well, wakes up refreshed and accomplishes all of her tasks for school work and even may do some chores. But those bad days man they are doozies here lately. We had taken her off medication because she was homeschooled and we wanted her to learn coping mechanisms versus using pharmaceuticals as a crutch. Don’t get me wrong, modern medicine is AMAZING, but she is still developing all of the things that will make her who she is and I (we) are not fans of what some medications can do to a developing young person.
Then we have the oldest of our girls (the ones I gave birth to) and she has dyslexia and asthma along with an old shoulder injury that acts up from time to time. She is a real doll and my biggest helper and cheer leader. She is so dang smart, until you put her on the spot to read something and then she sort of shuts down. She learns by doing and seeing things done. She loves a good story but reading is problematic and she has lovely handwriting because her stubborn little butt sat down and hand copied the library books she brought home and PRACTICED her pretty handwriting!! I let her use my kindle a lot because it has text to speech and she can make pretty much any book an audio book and I try to help her understand literature by having her follow along the text to audio or watch a movie or play versus reading them. She has pretty darn good instincts too and is sensitive to energies around her and that may come in handy with the horses she plans on training.
We also have Babyboy in the house, he is almost 6 and he was our unexpected surprise baby!! Like for real the doctor congratulated us and apologized in the same breath!! He is an awesome little dude. SO articulate and he loves Farming Simulator and Minecraft and videos of people doing things and building things. Think planes, trains, and automobiles and that pretty much cover it and LEGOS, cannot forget about legos!! He is a boy alright and also loves to be outside and get dirty but hates to take a bath and wash his hair. He is a real snuggle bug too and is so very generous with smiles and hugs and will absolutely out of nowhere tell you that he loves you.
You may have already noticed that Big boy and Big girl have left the nest to pursue other things and for that I am humbled, grateful, proud, and just a little sad. I will when necessary update on their young adult lives but my focus on this blog is the journey of life and those we encounter so be prepared to meet some characters along the way. And while it seems like time has hit fast forward in some places and in others its as if someone has hit pause. How can that be?? My kids are all growing up and getting older and yet we still seem stuck in the same situation. Faith is the hope in things not seen. Giving up is not an option when someone is calling you mommy. Love and light readers. God Bless ya for reading!

I smell fall y’all!!

by Mothersense, posted in Kids n such, Messy Life

Oh so much goes on behind the scenes here at Mothersense!! I have a new moniker to add to my collection “Jules the Mascara Mom.” It goes with my Younique experience and that comes into play with all of my other mothersense!! With the changing leaves of Fall so there are many things that change around our household!!
1)The Big Boy has left school and is now living with my parents across town. He has a job and is saving for a truck. He is also considering firefighter training or police academy!! He even paid his half of the cell bill this month!! WHOOP!! I am all about the baby steps!!
2) Big girl (not her birth mom, just her Jules) has moved off to her higher learning institution and is settling in well!! We hope she visits often because we sort of miss her and her spunk and green hair!
3)The other 4 rugrats have started back to their homeschool lessons. And co-op starts next week so we have to at least pretend that we have it all together! These guys are the ones that keep me on my toes! Fighting over computer time. Arguing about what all has to be written in the log book. Timing one another for their journal activities. Whew what a fun bunch! I am telling you the excitement about all of this school work is palatable. All kidding aside we have been very blessed to continue on the homeschooling journey and not have too many hiccups. The flexibility is really the best part because I can CUSTOMIZE their lessons to interest and engage them so that they want to learn!! Yay me, I call that WINNING!
4) My journey as an entrepreneur is still in full swing. I have always loved being my own boss and have made multiple attempts with Network Marketing and I really hope this time we can launch something I can have for years to come and my kids can be super dee duper proud to be associated! Younique is a company that makes amazing cosmetics. The Younique Foundation is on a mission to keep an open dialogue about sexual abuse of women and children! We gotta keep on keeping on!!
5) Hubby has seen his primary care doctor and his optometrist this week. Good news is that whatever is causing his pain and neuropathy is not affecting his eyesight. The bad news is that we still do not have answers as we are waiting on more MRIs and a consult with a neurologist. The primary care doc suspects MS and is treating for nerve pain and of course the degenerative disk disease, but we wait for now. And we pray and we do not give up hope. It is painful to watch my once vibrant husband reduced to such frailty that I have to help him off the toilet and up and out of chairs. He is only 37, it hard to watch, y’all!
In closing if you haven’t noticed yet http://www.julesthemascaramom.com is live and ready for any orders.
Also julesthemascaramom.net will route you to this blog where you can keep up to date on what is happening with us. The journey we are on with homechool, hubby’s disability, daughter’s special needs, and just LIFE in general!!! Subscribe below

Oh Ya’ll – Depleted didn’t even begin to cover it!! But it’s ok

by Mothersense, posted in Messy Life

I used the word depleted in a previous post ya’ll…I had NO IDEA how STRONG and RESOURCEFUL I actually can be!! When you are down you are in the best position to pray, and I have!! I have had people praying for me and honestly I can FEEL it!! I can also FEEL so many people counting on me to make this work. Whew!! We are in July 2015 at the tail end of it! The 6-15 year old kids have started back to their lessons everyday, we are still eeking out enough help here and there and odd jobs to pay the bills…most of them. I’ll tell ya what though I LOVE the strength of my friends and family for carrying me through!!! Without the people around me I probably would have gone batshit crazy by now. My oldest has 2 tattoos now,*sigh* and has decided he wants to work instead of go to school. My parents are aging so much each week I am truly scared that our time with them is limited. Have one more leaving the nest next month to head off into college. My youngest daughter is grinding her teeth pretty regularly in her sleep and may be the cause of her headaches but we still get dont-worry-about-a-thing-every-little-thing-is-gonna-be-alright-37to consult with a neurologist! YAY (no not really) Hubby’s medical issues are managed, we do know that degenerative disc disease plays a part of the pain but it is not the whole issue. Doc has said he may never drive a truck again. Right now he canot bathe alone and has fallen several times trying to get to the bathroom. Ladies and gents this is my row to hoe and its tough but there is a wise sounding 18 year old that once told me: “Every Little Thing Is Gonna Be Alright” aka ELTIGBA…and I love her for it more than she will ever know!! When I am depleted I look to those around me, I count my tiny little blessings and Thank God he gave me a new day to wear all my many hats that I wear each day!! Love and light folks!! Make today count!!