Artist Thoughts: The Color of Healing

First dress in 30 yrs

I recently purchased a new dress for the first time in over 30 years. I’d been wanting a kaftan so I purchased a pink tie dye kaftan. That got the ball rolling and lead to dress number 2.

When I was a child I didn’t wear much white because I tend to wipe my hands on my clothes, but unfortunately my family attached my worth to the color white. Here’s what I mean –

In 1992 I was getting ready for a function so I was ironing my white skirt and blouse. As I ironed, my sister kept walking past me saying, “Whore. Whores don’t wear white.” My mother and she were cruel. They wanted me to feel low and loathsome.

My sister was truly a piece of work. I got married in white and I could hear her evil words on that day, too. Fast forward to 2022. Not only am I older, I’m mad now.

I’m upset that my family attempted to harm me in whatever way seemed good. I was shamed so terribly over getting white dirty. It was always such a big ordeal. Living in the house with those two, I knew I was out numbered.

Recently I’ve been trying to reclaim a few colors associated with abuses. I’d been working on yellow for a while. I can say with pride that I have successfully reclaimed the color yellow and restored it to its proper place; next is white.

I’ve been tossing this idea around for a bit. It’s finally coming to fruition. I purchased a long, solid white Kaftan…..to paint in… to purposely wipe my hands on and get it all covered lol. Then of course I thought, what about shoes? So in February I’ll get a pair of knock-off, high top Converse, white for about $20. Converse right now are $115. I’m not trying to make that expensive of a point. Lol

Where the label on the shoe should be, I’ll put a sunflower. To tie the whole statement together, I’ll toss in a white dreadlock wrap and some hoop earrings.

I’m going target a few areas where I have unresolved issues such as over the heart, the lungs and the tassels at the bottom.

Colors of significance will include deep shades of purple bc the purple survivors ribbon is for Lupus, Domestic Violence and Dementia. All of these have touched my life significantly.

I don’t know when I’ll say the dress is “finished”. I do know I’ll wear it around the house to paint in. My paints are permanent and vivid.

A bit of irony – the dress arrived very wrinkled. I absolutely have to iron it before I put it on.

The rest of life is as troubled and discombobulated as everyone else. I’m taking it day by day. I find the world increasingly difficult to manage. I’m worried about the havoc politicians will reek on their world playground during elections. I’m not looking forward to racism being encouraged. Thank goodness I don’t understand the joy people feel when “sticking it” to someone else. But they love it.

While living in excessively violent times, politicians gleefully spit rhetoric to inflame groups and turn people against each other. It’s like it’s a billionaire’s game where the one with the most casualties wins.

Other than that, the frogs are great and so is Joe. The jumping spider is doing well. My CNA situation is “interesting”.

I’m a bit lonely right now though I see people regularly.

Rumination is pretty bad still. My emotions get intense but not like months ago. Sleep is too much or too little. Appetite is zero still, and last but not least menopause is kicking my butt.

At least I’m not as reactive and emotional as I was. I can catch myself sometimes, before I start, but it can be difficult to stop once started. I feel shame because I don’t feel I have the control needed to maintain interpersonal relationships. I’m worried about it. We’re still tweaking medication though.

That’s about the size of it.

Jordan

My Goals are Still in Sight

New big ol glasses

I’m still rolling. 🙂

What an exciting few weeks. I went from mourning my old CNA to getting a new one with whom I am very well matched. Having her means I can let her do some things and leave other things to me. I can keep up with my letter writing and other forms of reaching out to people. And I can keep up with my artwork.

My goal was to re-open my Etsy shop but I’m not ready for that. I can paint and sew but right now I need to wait a little while longer. I’m ready to do the art, I’m not ready for the stress of opening up the shop and getting stuff out on time. The goal is to do so but at this time there is no tentative date.

I’m pleased that rumination has decreased, which makes thinking much easier. The depression is better under control, and my physical health is holding steady. Concentration is crap. It’s awful but at least I’m completing things even as I bounce from project to project. I have zero concentration any more.

Anxiety is wicked. I’ve changed up how I do my Delta-8 so that it will help with anxiety more and kick in sooner. Sadly there isn’t any guidance on this. It’s trial and error, but at least it’s still federally legal and the cost is still within my means.

THC brownie bites

I baked refrigerator dough cookies and brownies. I cut them into dose sizes then dripped liquid THC over the top of the goodies. Works like a charm. It can be done with THC butter, too.

THC cookie bites

My metabolism is deathly slow which is why it takes 2 hrs for a bite size edible to kick in. It lasts up to 5 hours though.

Pain is not my friend. Anxiety isn’t either, but the depression and physical pain is significantly less, which has raised my quality of life. I’m still a bit reactive but not even close to how I was. Eating is a chore but that is getting better, too.

Wow. Food prices! No matter how much food costs increase, my budget for food has not. It’s been stuck at $200 a month for a while now with no sign of change any time soon. I’m blown away by food prices. I’ve been trying to see where I can clip pennies but I’m not sure where anymore. Perhaps it’s not totally a bad thing that I have zero appetite. Amazon Fresh is so high right now that it’s straight up robbery!

Menopause – well, I haven’t gone to jail yet. A terrible hot flash at least once an hour. Decreased ability to handle stress. I click on people! An Amazon employee had me so frustrated that I asked to speak with someone else. She said, who? “I said, I don’t care, anyone but you.” I really wish I didn’t say that to her.

So, things are progressing in a manner I couldn’t see 6 months ago. I want to remember that even in the worst circumstances, everything changes. And since I am involved and invested in life, chances for positive change is strong.

I’m happy I lived long enough to truly believe and trust that things change. Youth doesn’t provide enough life experience to fully grasp that things change for the better and you can move past what feels impossible. I wish my brother could have understood that.

Writing another page of life

Faith – Morton’s Pride

Life in Pictures – The Assignment

My abandonment issues have raged since the exit of the CNA I adored. She’s been gone for a week now. It’s affected my trust issues, paranoia and OCD issues. Going through the week with her knowing she would be gone in a few days was rather difficult.

I can feel the anxiety and emotion in my throat. I’ve been dealing with it by concentrating on art, plants and the cat. I’ve done so very little volunteer work. Argh.

Poor Joe is going to need a lightweight shirt to wear for the winter. My menopausal symptoms have affected heating the apartment. I can’t take this heat! I had it so the heat would come on at 65 degrees even while I have an 8 inch strong wind fan blowing on me. It’s not good right now LOL I’ve only turned the heat on about 3x since the season changed. How is it possible to be anemic and have hot flashes hourly, daily!

There was a day again where Joe seemed to have trouble with his front paws so I made him a bed, this time it’s on the floor. I would have made a box bed for him but my cat hates boxes. He doesn’t get in them. As a matter of fact, Joe runs when he sees a box or plastic bag. Yeah, he’s odd.

I thought I’d try to track the barometric pressure so I can kind of anticipate his arthritis pain and mine. Getting too cold will only make matters worse for him. I hope getting a lightweight shirt will help. It needs to be light bc cats can overheat too easily.

When Joe isn’t wearing his shirt I could let him use his bed with a safe heating pad that auto shuts off every 2 hours. I can set it to a low temperature and put it under his blankets, like I did last time.

I’ve done nothing more with designing Frog Mansion. It’s set up nicely but it’s not finished. I’ve done nothing to the Tomato Frog Apartment 🙂 I’m not calling it that LOL It’s just that it pales in significance beside Frog Mansion where my Australian Green Tree Frogs live. Anyway, I intend to work on it at the the beginning of December, at which time I’ll also add more soil and leaf litter to the Mansion.

Putting many of my houseplants in the mansion didn’t give back as much space as I thought but it has helped me simplify my watering system. Now I water plants 3 days out of 7 instead of daily. And it only takes anywhere from 20 min to an hour to water. I love how simple it is now.

I’m uncertain if I spoke of my hope plant. I’m seriously in love with this plant bc it’s name is my favorite word; hope. It’s in the peperomia family, which I’ve come to enjoy lately.

I would be lying if I said I’m not going to buy more plants but I will say they’ll have to wait bc I’m going to need paint. I’d like to get to Hobby Lobby but I don’t think it’s going to happen. It would save money though. I’ve never purchased from their website.

I’m stuck on the art piece in the photos because I now regret adding the ghost-like memories leading to and through the house. I’m not certain how I’ll make it look right. I’d remove them if so many other images weren’t dependent on the ghost-like memories.

I’ve got a completed painting that I’m determined to completely seal by Monday. I seal paintings in very small areas at a time because I don’t want pooling, running or gaps in the seal. I’m not going to spray it, so it’ll take a little time.

I’m not sure why I’m procrastinating. In general I’m not a procrastinator but I’ve been putting this off for 3 weeks. I’m having trouble letting go. I think I’ve been unsettled and I’m holding on to things.

To also unsettle me are the recent mass shootings, three back to back with a horrific quadruple knife murder. I don’t even know how to process this stuff and manage my own horrors.

I check the news online once a day, from various sources.

I will continue to have zero friends on my Facebook page so I can limit the amount of exposure to politics and the hatred it produces.

Despite the fact that the world has gone mad, I feel 99% like my normal depressed, anxious, dissociative self. Do I feel strong? No. I feel prepared and supported. I feel I better understand this part of the assignment.

Faith

Bonfire. Dissociative Identity Disorder.

Bonfire. The most exciting news is that I was able to go to the bonfire my friends had. It was wonderful! I got to pet a cute puppy ??. Then when it got dark the kids put glow sticks on. They made glow stick glasses, ears and bracelets then played tag in the dark. It was one of the most pure things I’ve seen in a long time.

Sitting there with my friends I thought back to when I asked why I even survived the events of 2018. Life was unbearable and I wonder why on earth I survived just to feel so hopeless. Now the public health emergencies have ended and I don’t need to isolate any longer. So I went to the bonfire and laughed with friends I’ve known from 10 to 30 years. There were smores, BBQ and innocent fun. That is why I survived 2018. Moments like the night of the bonfire, that is what I survived for!

I was in the hospital 2 weeks ago which totally freaked me out and triggered PTSD issues. I managed it though.

I had the opportunity to put my feet in grass again, which was the first time since the amputation. Unfortunately, I can’t feel the grass anymore, there’s just not enough feeling in that foot. Later I thought about how I can put my palms in the grass instead of trying to feel it on the surviving foot. It’s also come to my attention that I can do grounding / earthing with the palms of my hands …… I find it interesting that when primarily people of color didn’t wear shoes it was a reason to call us uncivilized. Now it’s earthing / grounding.

DID and Mental Health Its noteworthy that during my mental health breakdown during the pandemic, I had a split. I’ve done so much work integrating but I’m susceptible to splitting again, and I have. I talked to Dr D about it bc I recognized 2 people here who had been integrated. It’s taken a few months for me to be certain that Maureen and Crystal have split off again. I’m not a doctor so I can’t give specifics on how, but I’m 100% certain of it. I’m kind of embarrassed.

It was the assault that sealed my decision not to further integrate. I have who I have. Lol. Of course I’m staying in therapy, it’s just not with the goal of integration.

So this is my long, drawn out entry about all that’s happening over here on Sundrip and in the last few weeks. ???? Some things are trying, but I’ve made a lot of progress on the new psych meds. I’m pleased with the spot I’m in. I can now stand to be in my skin.

Thanks for hanging in and reading my updates.

Until soon,

Faith

Uncertain Title – Work in progress

Several years ago I painted two sisters on vacation. They were under the hot sun in summer dresses. There’s a whimsical feeling to it that makes me smile. But the painting / collage of the mother and two children in this entry, gives off an entirely different emotion for me.

When I look at the cropped painting below, I see a family that has traveled a very long distance. What drove her to walk across inhospitable terrain with children? What they are seeking must be worth the danger and inhospitable terrain. And then there’s still this question; Has the family successfully made the journey or do they have further to go?

The mother’s hair branches out like a tree while the hair of the children is circular. I see a difference in the expression of the children, too. The other thing I see is a family that’s held on to tradition for a long time.

I’d say the most striking part for me is the amount of movement, contrast and texture in the whole of the painting. The background itself could tell you it’s story, if only it knew where to start.

I really enjoy using parts of my own art as collage pieces. I use cut outs from art I did, but it didn’t work out. I keep a box of those art pieces so I can use it for something later. I’m working on two more collages in different stages of completion. I think collages speak to me right now, but that’s an entirely different blog entry 🙂

What should I name this piece? I have no idea at all. I’ll have to figure it out soon because this is a piece I don’t intend to keep.

Until soon,

Faith

Words to yourself matter, choose them wisely

Over a week ago I saw my nurse practitioner. We talked about the PTSD from the hospitalization in 2018. I told her that I just can’t paint anymore. I added, “When the legs failed and my foot was amputated, so too was the art in me.” Well, I’ve said that before. I’ve been saying it for nearly two years, but that time I truly heard myself say it and I knew I believe it. That’s a problem for me. Don’t tell me I can’t do this anymore. I was mad at myself. How dare I speak to myself that way?! I can’t be the person I was born as? I won’t accept that.

Point blank, I was born an artist. That art comes in many forms; culinary arts, painting, making dolls and creating terrariums. I’m driven to make things in an artistic way. The only way I stop being an artist is when I stop breathing. It was close back in 2018. Even still I want to be in an artsty urn. It’s already been chosen cause y’all can’t put me in any ol’ thing. I’m just happy I’m not in said artsy urn right now.

When I realized I actually believed that I can no longer paint, like I said, I was mad. Later that evening I got out my paints and started painting. While painting I remembered saying something very important to myself – It doesn’t matter if it’s good, just enjoy the process. That’s the moment things changed.

It doesn’t matter if it’s good! I was willing to have the art piece fail and that is significant. Before getting new depression meds and having a little more clarity, I was too afraid to fail. It felt like I was a failure instead of the art piece not working out. But this time I didn’t internalize its possible outcome. That’s how I know I’m in a different space. I was able to separate the two. I’ve been painting for over a week now. I’m risking a bit more and it feels good.

I didn’t die in 2018. I’m still an artist through and through. Regardless of any amputation, there’s no way to amputate my art. I can’t tell you how relieved I am. I worked hard to get to this day. Oh my goodness I worked hard from the day they told me I wasn’t going to make it until this day. I’ve worked hard. It hasn’t been pretty, at all. Some things I messed up beyond fixing. I know I’ve hurt people by spilling anger or responding while unhealthy instead of just walking away. Why did this happen? Because I’m a speck of dust like everyone else and I do and say reckless things. But I am not a vicious person, just a profoundly imperfect one battling mental health and physical health.

I understand something now. You’d think I grasped this four years ago but I didn’t. I understand that I didn’t die in 2018.

My entire life changed. I can’t walk anymore but I’m alive. I’m extremely limited, but I’m alive! The person I knew myself to be left the hospital and the nursing home, then moved here. I don’t need to be afraid to live.

I was living this life of “why bother, I’m just going to fall over dead anyway. ” I was afraid to live, make attachments and risk a little because I just didn’t want to lose anything else. I feel like I lost so much in 2018 that the thought of losing anything else was unbearable. I was afraid to live. I’m in a better spot but I’m not OK. There’s so much more physical healing and emotional healing to do. I no longer worry I’ll have to endure it without my art.

What I’ve learned is that I believe the words I say to myself. I know you reap what you sew. If I plant tomatoes I get tomatoes. It works that way with words too. I was planting fear in my garden and that’s exactly what I got. Words matter. What I say to myself matters.

Art work – The painting changed quite a bit from when I started. It’s a collage now. And true to form, I’m working on multiple art pieces at once. My studio mascot Joe Schmoe is helping with quality control. He’s such a good studio cat and mascot.

I’ve been putting art in people’s homes since 2007. My 2023 art goal is to fill my own walls with my artwork. It’s time I did that. I’ll give an Etsy update soon.

Speak kindly to yourselves,

Until soon,

Faith

Stand and wait

I will wait

I know how it feels to be so broken that it felt as if I’d die where I lay. But it’s true, if you hang on for one more day the urge to act in a permanent way will not be as strong.

When I couldn’t pick myself up, even after the wait, I reached out and my friends reached back. I’m grateful for that.

Faith Austin – Sundrip

Therapy Review: Sundrip. Death and Dying

Content: Self love. Sundrip and social media. Death and dying. Sexual Assault.

We talked about shame and guilt. Guilt is for actions but shame describes who I am.

Self Love. We talked about fear as it relates to self love. I fear saying I’m worth loving because doing so means I have to fully accept that my mother was wrong. To a certain degree I still deny the full impact of her actions and what she allowed.

I know I have self love to a certain degree. I said I love you to myself for the first time ever.

An opportunity for further targeted psychological treatment has opened up to me. I’m not in the mental health space to accept it but the offer stands. The practitioner, aka Hippie Therapist, will allow me to video conference. This doesn’t replace Dr D.

Sundrip. I’ve said several times over the years that I’d like to walk away from Sundrip.com as it is now. I know in my heart I can’t simply shut things down. Sundrip is my baby, but I think it’s time to bring this to a change from what it is now. It has been definitively decided that I’m closing the blog part of Sundrip in five months time. Why 5 months? Three months are too few but 6 is too long. I need to take gradual steps. I’ve set a date.

This is going to be difficult but needed. The world has changed since I started this blog. The internet has changed. Honestly, I fear I have too much to lose by continuing as is.

Death and Dying. We spoke about how I gasp and sit up in bed because of feeling like I’m on the gurney, at the hospital being wheeled to a surgery I wasn’t expected to survive. That was 2018 but it still haunts me. For days I said goodbye to my friends. We wept and supported each other. I apologized for the hurt I was causing by being in that condition. I said goodbye to my long term therapist. I so did not want to hang up.

It felt like I had been given the death penalty and that at 11am (?) I was going to die.

That hallway was long. The room was cold. They asked me to take a deep breath. It felt like I was participating in my own death. I wasn’t supposed to survive that, so I felt like I was asked to take my last breath. Breathe deeply and go to sleep w a 15% chance of surviving. I took a deep breath in and exhaled the name of my God. The anesthesiologist was brilliant and supportive.

When I woke from a surgery done only a few times in the United States, the nightmare wasn’t over. Did I survive a 10 hour surgery only to bleed to death? The nurse held my juggler closed with her hands because I would not clot. Another nurse held the artery in my groan. Other means to stop the bleeding were used too but the main way they got it to stop was to clamp them manually w me awake.

Despite the violence in my childhood, I never begged my mother for my life or for her to stop. In the hospital that day, w the sheets turning red, I begged the nurse to please not let go. She said she wouldn’t. She said to be quiet, turn my head to the left and look up. Eventually I woke up in the arms of my friend. The first thing she said was, I never knew you were this sick. This is Lupus? She held me.

Amazingly, I only have one physical scar from the surgery to get all the blood clots. Despite the foot being dead, I had to wait 2 more months before they could amputate it. The skin began to slough off. That sight is burned in my head.

The recovery room after the blood clots surgery was interesting. My bed was in the middle of the room. It tipped in different degrees, went all the way to the floor and quite high up. I had my own nurse. I was her only patient. I still remember her name.

There was a large area w homey furniture to the right and down a step, other friends were allowed to stay. I was in complete shock and so was everyone else.

Daily, for five months they took my blood directly from the vein, not the IV. I understood why but it still felt like torture. Changing the bandages on my new stump sometimes took 2 hours. It was torture. I felt like I was going to crack.

Dr D and I are discussing possible emotional and cognitive issues as a result of the stroke. We don’t feel that Pseudobulbar affect (PBA) applies to the fullest extent, but we are exploring emotional differences since the stroke.

What I’m aware of at this point is that I’m unable to emotionally or physically cope. I feel like my insides are missing and have been replaced with a dark hole and overwhelming despair. I don’t feel like I can reach inside for strength because I feel hollow.

In 2020 I was assaulted. Where am I safe? How do I protect myself? I’m afraid.

I need mercy.

Faith

Half a Century More

I started this little painting back in October of last year but I just now finished it. It looks so much better in person than the terrible photograph. This 7×10 watercolor piece has a lot of numbers on it. The numbers are ages that were very significant to me with age 47 being the last significant age on the painting.

The painting shows a young girl who divides the paper. She’s a young me with a split face depicting multiple personalities. Though I don’t know the exact age I split, I’m sure I was fully a multiple by the age of nine. I have a few symbols in the painting like a peanut and a purple butterfly as well as a wheelchair with a sunflower instead of a wheel.

One of the most significant things about this painting is the tree. It is bare on one side and full of colorful leaves on the other. Though they’re fall leaves that are technically dying, the point was to have colorful and lively leaves like seen in the Fall, which happens to be my favorite season.

I call the painting Half a Century More because of what a friend said to me jokingly the other day. I told her I’m about to turn 50 and she said, “Oh, you’re going to be half a century old.” Well I tell you I was floored!!! Wow. Do you have to put it that way? It took a few days to kind of get settled with it but now I think to myself, I’ve lived a half century but I’d like to live a half century more. I’d like to have a lot more art to paint, dolls to sew and days to figure out how to be happiest.

I won’t be 50 until August but I’m so, so exited I can’t stand it. I honestly never expected to see that number. For many reasons I didn’t expect to be here but half a century on and I’m still kicking!

Faith

Lola – Queen of Sorrows

Lola

She accurately represents how I feel often. I wish I could say that I’m okay and that life is good. I mean really, complaints should be few but in general I’m not a happy person.

I named her Lola because in some languages it means Our Lady of Sorrows. It seemed so appropriate.

Lola is my third handmade sad doll. I made her with real hair this time instead of yarn. I really like the look. Lola is in my personal collection and sits where I can see her each day.

Some have described her eyes as knowing and with a story to tell. I just think they look wide and sad, much like my eyes as a child.

I made Lola a little sister named Victoria aka Victory. She’s not a sad doll. As a matter of fact, she’s a doll that is at peace. She’s not grinning but she is full of life and innocent. Victory is also in my private collection.

Victory

Now comes Grace. Grace was to be the 4th sad doll but she ended up not looking so sad. I like little Grace.

Grace

I like her wine colored dress and the bow in her hair (not shown in the photo). She’s wearing a second-hand Gloria Vanderbilt dress. I couldn’t believe I found that little tiny dress. It’s just adorable. I added a small heart button and put the tiniest, little gold details on it, not much though. The dress is simple which is what I like about it. I added a small piece of gold hair jewelry to her long, braided, yarn hair. Little Grace will be going home with my new nurse’s aide next week.

So while I deal with some sadness and depression right now, I’m out here making dolls and doing my best to manage life.

Faith