Thursday, March 26, 2020

Coronavirus Escape: Burnside Island for Guilford Park Pre-school and social distancing ART WALK in New Irving Park

Hey guys,
I don't know about you, but I'm getting a little stir-crazy at home. This weekend (Saturday, March 28) from 10 a.m.- 12 p.m., we are having a neighborhood Art Walk in New Irving Park. If you live here, come on outside and walk around to see if you can spot the artists who make this place our home!  Check the New Irving Park neighborhood Facebook page for details. We are going to set up art in our driveways and you're welcome to take a peek. Kids can join by making their own art to display- really anyone who wants to display can jump in the game!  Please do! The more the merrier.  This is intended to be a fun distraction from the Coronavirus pandemic. Feel free to say hi and chat with us- but let's keep that social distancing in place for everyone's safety.

You can see this painting (and several others) in person and make a bid once the Guilford Park Pre-School silent auction website is up and running.  Check it out! I'll share the bidding website once it's available (definitely by April 1st).

Check out my time-lapse video of how I painted this piece earlier in March.

Stay safe and remember- we're all in it together.
socially distant xoxo's

Thursday, August 8, 2019

Fall Art Lessons 2019

Hi Parents! I have options for both elementary and middle school students this fall on Thursday afternoons. Here are the sessions.  If you'd like to join, just message me and you can reserve a spot for your student. Space is limited, so please let me know as soon as you can. I'll send you the details. Thank you!

Elementary School (2nd- 5th grade) Thursday 2:45-3:45 p.m.

ART SHOES! You bring a pair of canvas shoes- any style or brand (in your size) and we will plan, design and paint your very own wearable art! Think  about watermelon sneaks, flower power or even your version of Van Gogh's Starry Night if you're up for a challenge. 
Sept 19 
Sept. 26
Oct. 3
Oct. 10

Holiday Art:  Gingerbread and Mooseltoes!  Would you rather have a holly garland or some snazzy ornaments on your moose? Either way, he will be ready for the holidays! Paint two beautiful creations with me for some holiday fun.
Nov. 7. 
Nov. 14 
Nov. 21 
Dec. 5. 

Middle School (6th-8th grade) Thursday 4-5 p.m.

Art SHOES! You bring a pair of canvas shoes- any style or brand (in your size) and we will plan, design and paint your very own wearable art! Think  about watermelon sneaks, flower power or even your version of Van Gogh's Starry Night if you're up for a challenge. 
Oct 3. 
Oct. 10 
Oct. 17 
Oct. 24 

Holiday Art: German sparkly Putz house.  Do you know what a Putz house is?  It’s a beautiful tiny home made from cardboard, paint, glue and of course- glitter. We are going to create miniature masterpieces that will sparkle all the way into the new year!
Nov. 7. 
Nov. 14 
Nov. 21 
Dec. 5. 

Monday, May 6, 2019

Greensboro's First Walk for FPIES

Super Moon over Bald Head Island
2019, oil on canvas, 30 x 40 inches

Drawing:  For a chance to win this painting, please click the link above and make a $5 donation.  In the comments section, please leave me your phone number and I'll contact the winner after the walk. You do not need to be present to win, but you do need to be able to pick up the painting or cover shipping costs. Thank you so much and good luck!

Who: Help us help my daughter and other families with FPIES
What: A Benefit for I-FPIES (a nonprofit that supports medical research for FPIES) 
Where: Greensboro, N.C., Country Park
When: Sunday, July 28, 3-5 p.m.
Cost: A suggested donation of $25 is requested to fund medical research for FPIES 

The event will include a 1.5 mile walk on a paved path (great for strollers), as well as a drawing for the painting above.  Families are welcome!

Sweet Georgia's Story: 
I need your help. It’s hard for me to say that because I don’t like to ask anyone for anything.  But you see, my daughter has a rare disease and I can’t cure it alone. Together we might be able to make some real progress.  If you know me at all, you know this disease has turned my world upside down. Trying to figure out the puzzle of how to nourish my child has baffled me, consumed me and made my soul both shrink and swell. It has given me a purpose like you wouldn’t believe. I never thought I’d be the mother of a child with a rare disease, much less a disease that precluded her from eating healthy food or most any food for that matter. I was afraid of many other things while I was pregnant. What blindsided me was the diagnosis that came months later. I had no idea that a disease like this existed, but what still tears me apart the most is that there is little to no science to help me navigate this nightmare. We can change that together. We can change that today. 

You’re probably curious about it. I am, and I’m happy to talk about it. It’s truly mindblowing. It’s awful, but there’s a strange glimmer of hope because maybe she will outgrow it. 

 “I think it’s FPIES” our pediatrician said at the 6-month wellness visit. He asked me how solid food was going and I just replied “It’s not,” and laughed nervously.  We had been through the wringer with a difficult pregnancy marked with lots of vomiting, strange problems and an infancy that was riddled with colic, non-existent sleep and profuse foul diapers. I just thought everyone’s experience was like that.  At two months old, I took our daughter in to the pediatrician again because she screamed for three hours straight. She was covered in eczema. She was spitting up 5 or 6 times after every two- hour feeding. She couldn’t fall asleep (obviously) and I know what you’re thinking. You’re thinking what everyone was thinking. Babies are always hard. Babies never sleep. Babies spit up a lot. Babies have weird diapers. Babies cry. Yes, all that is true, but this was different and exponential in the nature of difficulty. I now have a name for it. It’s called FPIES. You pronounce it Eff Pies. The name is amusingly appropriate.  

Around the 2-month mark, Georgia had several seizure-like events that I now know are called Sandifer’s syndrome. My husband called me home the first time I left the house to get a break. I was having dinner with friends and I still remember the panic in his voice and the painful cries of my daughter in the background. This was the hardest time, until the next time it was the hardest time, and the next after that. Sandifer’s syndrome is caused from excessive reflux that is so painful it makes infants writhe and jerk their heads back in seizure like movements. She was allergic to foods that I consumed and my breastmilk left her in pain. Around the same time,  her stomach became grotesquely bloated and her belly button went from an innie to an outie almost overnight. That was an umbilical hernia, but  it was protruding because of inflammation in her gastrointestinal tract. Terrified, I took her to the pediatrician and all I could say was “I know there’s something wrong, but I don’t know what it is.”Luckily he believed me the first time. Other FPIES families don’t always have the same luck.  

We were initially diagnosed with cow’s milk protein allergy and I was instructed to cut dairy and soy out of my diet. After a few days with no improvement, I was radically in need of some help, so I switched her to Nutramigen formula and that worked wonders within 24 hours. Later we would lose this formula too, but at the time it was a life-saver. Some FPIES mothers drastically alter their diet to continue to nurse their babies. They lose so much weight that their own physicians worry about their health. Because any food can be an FPIES trigger and we have to eat multiple times every day the experience is like tiptoeing through a mine-field. I’m glad I tried the formula. I never would have been able to cut out all her trigger foods from my diet while breastfeeding. It took me over a year to find out that she could only eat eggs, broccoli, olive oil and salt, and the broccoli was an addition that came months after the other safe foods.  

We wouldn’t hear about FPIES or have a true diagnosis for several more months. Some families don’t get a diagnosis for years. I felt strange when I first heard it. Eff pies? Hmm that sounds funny.  It stands for Food Protein Induced Enterocolitis Syndrome.  But to me, it stands for Food Poison is In Everything, Sweetheart.  

My Georgia can’t eat most foods.  You can’t tell by looking at her. People find out and the first thing they say is, “But she doesn’t look sick!” Yes, I know. She’s not malnourished. She’s smart, beautiful, kind, mischievous, compassionate, silly, defiant, delightful, wild and she’s perfect because she’s ours. We love her and her brother beyond measure. She looks healthy because I have figured out what doctors could not tell me. I have figured out her safes, as we like to say. I use the word I because my husband has been working hard at his job so we can afford her formula among other things. I handle the food trials and the doctor appointments. I keep the food diary. I shop for food- searching- always searching- for single ingredient items that might work for her. I rarely find them, and even when I do, she reacts and we clean up vomit for days. I research this FPIES mess. I read posts on an FPIES support group via social media where other brilliant men and women from all kinds of careers are also desperately trying to find their way through this diagnosis. I attempt to find medical journal articles and scour them for clues. I learn about non-western medicine ideas that might help. I am skeptical, but I am desperate. What I want so desperately are peer-reviewed research papers and clinical trials with FDA approved medications and other medical tests that might help us navigate this, or know when and if it will end. Instead I make pancakes from broccoli. I stand up straight and I go scramble another egg and make another bottle. My daughter is two, for crying out loud. I have cut eggs into bunnies and flowers and made as many things as I can think of with the ingredients we have. I FPIES mom so hard. You know it. I’m proud of it too, because there is never a break. There is never a time when I can just order some take-out and relax. But I am strong. I am an FPIES parent. It’s a title I never wanted, but I have earned my stripes with blood, sweat, lots of dirty spatulas and tears. As an FPIES parent you quickly learn that YOU are the ONLY ONE who can keep your child safe, or advocate appropriately for your child’s medical needs. It’s both a burden and a superpower, but it is always earned the hard way. 

We purchase copious amounts of a special elemental formula for which our insurance company denied coverage “because it isn’t administered through a feeding tube.”Let me assure you, that formula is medically necessary for our daughter’s life and health. It costs us thousands of dollars a year and I am grateful that we can afford to buy it for her without going into debt. I am angry that our insurance has failed us in that manner. Having a disease should not dictate whether or not you can properly save for college, prepare for retirement or afford quality childcare. But it does for many families. We are lucky we can make it work as well as we can.  

Usually the next question we get is a disbelief of “How did you know?” It wasn’t easy, but every time we fed our daughter, she got sick—really sick. She got so sick that she was vomiting and dry heaving for DAYS. My super active giggly mischievous baby would lay on the carpet in our bedroom lethargic with her face down on the Fisher Price playmat. “It’s just a virus,” they told us at the pediatrician’s office when we brought her in three times one week. “It’s probably not over yet. I can hear gurgling noises with the stethoscope.” 

It wasn’t over by a long shot. I told the doctor (who was not our regular pediatrician) that I thought it was sweet potatoes or oatmeal cereal because it happened when we fed her. “No, an allergic reaction to food doesn’t look like that,” this doctor said. My mama instinct knew better. I stopped all food. I offered her the hypoallergenic formula and poof, my child stopped dry heaving and vomiting. Her rash cleared too. I had to test my hypothesis. Reluctantly, I gave her a single miniscule bite of oatmeal cereal and within 24 hours, she was projectile vomiting again and we were changing diapers, cleaning the floor and doing mountains of laundry for days. Life was so heavy I felt like I couldn’t breathe, much less get out of the house without tremendous effort. “Is motherhood really this hard?” I wondered. 

It’s a cruel diagnosis attached to a strange tiny glimmer of hope that may or may not magically happen for my daughter. I cling to that hope with all that I have because like any parent I want a life for my children that is free from the burden of a chronic disease. I want a fairytale ending to this tragedy. I want to buy my girl a Starbucks drink of her choice one day when she’s old enough for coffee and look back and think to myself. “Thank God that’s over.”  For now, I bury most of our troubles deep in my heart and repeat this script fairly frequently: “It’s okay. We’re doing okay. I have learned how to navigate this and maybe she will outgrow it.” These words are true, and our lives are good and full of joy much of the time. But things could be a lot easier. I say those words to people I meet who have offered something like a lollipop or a popsicle to my child that I now have to turn down for her safety.  

When I explain her diagnosis lots of people say “Well she’s so little, maybe she doesn’t know any better. Maybe she won’t remember it.”Trust me. My child knows. Every single day my sweet, smart daughter watches her whole family sit down with plates of food that have the colors of the rainbow- red bell peppers on a green salad, yummy macaroni and cheese, plump purple grapes and juicy blueberries. Sometimes birthday cake. Sometimes chocolate Easter eggs wrapped in shiny pastel foil. Holidays are hard. My child knows

She looks at her plate with eggs and broccoli and she lowers her pretty little toddler eyelashes. Her body sinks into her high-chair. She knows. Then she points to food she can’t enjoy as she perks back up and says gently “Miles eat dat.” She is happy that her brother can have it, even when she is denied much of the pleasure of everyday life. My word, she is generous. This isn’t right. This is terrible. This isn’t the life I want for her. I hold it together and try to keep the focus off the food and distract her with conversation and silliness when all I want to do is give it all to her- Let her taste it- Or cry. This just isn’t right. There is no end in sight. It feels like we are drowning. “It’s okay,” I tell myself.  Maybe she will outgrow it. 

My heart aches every day with a strange pain that I can’t describe very well. Then I feel tremendous guilt because yes, it could always be worse and “maybe she will outgrow it.” I have lightly comforted strangers with my words and my smile when my soul was cringing because my child is sick and nobody can help me figure out how to make it better or even keep her safe. Somewhere I read another FPIES mother’s account of what life was like at this phase. She said “It is hard to put into words how difficult it is to have a child who is allergic to most food.” I agree with her. I have done the research. I have read everything I could get my hands on. I know many children outgrow FPIES—In fact most outgrow this. But more than anyone else, I also know that there are children that do not outgrow this disease. I know this because I hear their stories too. My daughter has a severe case of FPIES illustrated by the fact that at age two, she can only eat four ingredients. I want so badly for us to be in that percentage that outgrows it, but our case doesn’t always look like the other cases and I worry constantly.  

Who wouldn’t? Even after people started to realize that I wasn’t just an overreacting mama bear--even after they started to believe that my child couldn’t tolerate my breastmilk or baby cereal or compounded Tylenol for teething or antibiotics or even a fraction of a cooked spinach leaf pureed and scrambled into her eggsEven after they started to believe me at the doctor’s offices- I still realize that the science to help my child does not exist. 

I want my daughter to enjoy the simple pleasure of a North Carolina tomato sandwich on kid-friendly Sunbeam bread with the crusts cut off. I want her to know it tastes even better by a swimming pool and magnitudes better when you call it by its true name, ‘mater sandwich.  I want to offer her a taste of the creamy pimento cheese that her grandparents sold at their grocery store for 35 years before she was born. Never mind that she might call it “yucky.”  Even that would bring me joy.  I want the luxury of being able to offer her food from my dinner plate or to go out to eat and have her order off the menu. You mean to tell me some people get to go out to eat and don’t have to pack special food for their children? I want that. I want her to be able to bite a juicy red strawberry from Rudd farm out on Hicone Road. I want to host a cookie decorating party like my mother did for the neighborhood posse of children. I want to give her a popsicle that isn’t just plain ice, again.

I would have LOVED to pass her a handful of toddler puffs, Cheerios or quartered grapes to entertain her as she sat in the highchair while I cooked a healthy family supper. Instead I entertained her in other ways, mostly by holding her while I did all the things. 

I had to keep her away from the dried bean sensory bin I made for our son before I understood the wrath of FPIES. I had to hold her, wiggling and squirming, all the time to keep her away from the crumbs on the floor at playdates and the broken goldfish on the ground at the park that might poison her body. My daughter did not want to be held.  She wanted freedom to play. She fought me from holding her all the time. I could never let my guard down because those insignificant crumbs littered by other innocent toddlers really could hurt her.  

Speaking of crumbs, I’d really love to be able to make some kind of bread for her. Do you know the cloud bread recipe floating around Pinterest? Yes, I’d like to cook that, or maybe something with almond flour or quinoa. We failed those foods too. In my wildest dreams I’d like to be able to feed my child a birthday cake. I’m not even talking about a cake with all normal ingredients like butter, flour and Dixie Crystal sugar. That might be too much to hope for. A homemade slightly lopsided cake I make with alternative flours, some kind of sweetener and coconut icing would flip my joy scales and hers to the max. Is that too much to ask? Maybe she will outgrow it. 

Instead, for her birthday cake I painted a hat box and put a plastic toy inside. She loved it, but she also watched her older brother eat cake. You see, this diagnosis means that most food gives my daughter a delayed allergic reaction that doesn’t look like the allergic reactions we are used to. It might take 2 hours or a month for the trigger food to start inflaming her intestinal tract. By a month in I mistakenly thought many foods were safe. Our pediatric allergist and immunologist who works with a significant population of FPIES patients advised me to try a food for 4 days and if she seemed fine, the food was probably safe. That wasn’t true for us. Physicians don’t have the information they need because this disease hasn’t even been characterized to understand the full spectrum of the disorder. 

If I don’t find and stop the poison masquerading as my homemade apple sauce, Georgia could vomit to shock with repeat exposure.  For us, repeat exposures escalate in severity. Every single time I try an ingredient, it gets worse and worse with each exposure. Some FPIES specialists tell parents to push through symptoms. Some don’t even believe in the existence of this disease or in the various presentations of it. Believe me, it’s real. We have tried over 40 foods in the past year and a half. There are 52 weeks in a year. You do the math. FPIES looks like a stomach virus that spans years, not weeks. Years. None of our food trials were safe for her except eggs, salt, olive oil, and broccoli. Following the advice of our specialists made my child sicker. I can’t blame them. They are genuinely working to the best of their abilities with the information they have. They don’t know how to help either. The science doesn’t exist yet. 

The foods I have trialed are healthy and simple. They are foods like apples, grapes, quinoa, coconut, avocado, banana, corn, rice, potato, pear, spinach, cauliflower, strawberries, watermelon, cantaloupe, green beans, carrots, rice, mangoes, and broccolini. I have not found a single grain or fruit she can enjoy. We get excited. We try a food. She loves it. Her symptoms begin. We try to keep going. We fail. We clean up. We rest. She begs for the food we can’t give her. We do it all again. Now I am just tired and frustrated. What I wouldn’t give for a medical test to identify a few more ingredients to feed my baby.My God I have tried so hard. 

One time I used pink Himalayan salt on her food instead of the regular corn-free salt that I purchased. I did it intentionally because her salt is non-iodized and I know iodine is essential for health in trace amounts. I worry about her nutrition all the time, so this is a normal thought for me. I sprinkled some pink Himalayan salt on her eggs. The vomiting started that night. Did she get something by accident? Did I use a different brand of eggs? Does that matter? Did she eat a crumb off the floor? Did I use the bagged frozen broccoli instead of the fresh broccoli today? Does that matter? Did she get a piece of cat food again? (Yes, this happens) I figured it out. The vomiting stopped. Another time I bought the wrong brand of olive oil in a pinch at the grocery store. It was blended with a cheaper kind of oil. Vomiting. You can’t fool my girl. She’s more sensitive than the princess and the pea. 

Last year we took the minivan to Hanging Rock, Tweetsie Railroad, and the beach. They’re joyful times. I post happy pictures. We legitimately have a blast. But every time we eat in the car, I hand my son a chicken nugget and I forget to clean my hands thoroughly. Then I touch my daughter’s food without thinking, handing it back to her in the car-seat. Two hours later she projectile vomits in the car. The only reason I know what triggers this is because it happened to us so many times that I finally put the pieces together.  Now here comes the fun part for FPIES parents. Was it the flour, the chicken, the oil it was fried in? Was it some additive? Welcome to the FPIES game! The only way to know what triggered it is to eventually pick one of these things, feed it to her and wait. No thank you.  

Now we use a fork to feed her in the car. She pulls the food off the fork and throws it on the floor. It is another kind of game. Over and over I throw away the food we carefully make for her because she contaminates it. We make more safe food. She eats some of it but she is tired of eggs and broccoli. My house smells like broccoli and hard-boiled eggs all the time. Yummy. My daughter likes to smear the egg yolks onto things. Things like carpet and upholstery. I get frustrated. I clean it up. Again. Why is it so hard? I wish I could give her some Cheerios. This is what an FPIES diagnosis looks like.

So why am I revealing our struggles? After all, there are much worse things than FPIES and sincerely, I know it. My life is wonderful and I am content. Do I want pity or attention? No.  Do I need encouragement?  No, but I am seriously grateful for all the help and kindness we have received in relation to this diagnosis. I am intensely proud of how we have handled this hard thing. I was strong before I became a mother, but now I know the depths of what I will do to care for my children. I bet you know those depths too because you have your own struggles.  

This post is about sharing our story in the hopes that we can make it better for those that come after us on this slog through an FPIES diagnosis. The words that I have both loathed and clung to over the past two years are “Maybe she will outgrow it.”  But now I am tired of hearing that because it means that  nobody knows how to help us. Coming from physicians, it means there’s hope but there’s nothing else we can do for you at this time. That’s not good enough for my Georgia or any of these children. 

If the resources don’t exist, let’s build them. Hope is a powerful thing, but actions speak louder than words and I am ready to act.  Please help mePlease help us unravel this mysterious disease. 
Come walk with us. Please donate. Your contribution can have a direct impact right now. Let me explain. FPIES research is scarce. We can make a difference simply with targeted funding and awareness. Here are my goals for the first Greensboro Walk for FPIES: 

Fund research to:
Create an affordable and accessible test to identify safe foods and trigger foods. 
Identify the root cause of FPIES. Is it genetic? Is it environmental? Is it both? 
Characterize the disease in its entirety so that physicians may have a set of solid guidelines to help patients navigate food trials. 

Raise awareness by:
Educating physicians so that they know how to identify FPIES before months or years have gone by without answers.
Ensuring that future families with FPIES don’t feel so helpless and alone in this journey. 
Helping local and regional FPIES families find each other because we desperately need each other to feel whole and sane. 

I believe we will continue to see this disease grow in scope. Just this year, the International FPIES Association announced findings that FPIES is no longer as rare as we previously thought. A large national allergy study found an FPIES diagnosis in 0.5% of the population. This research places the estimate of U.S. people living with FPIES at one million. ONE MILLION!

I believe many more cases of FPIES are undiagnosed because FPIES has a spectrum of severity and is often outgrown before identification. Let me explain. My son suffered from this disease too, but was never diagnosed. As a first-time mom, I thought everyone’s child was just hard. Looking back now I see striking strange similarities between our son and our daughter. Our son had constant reflux, vomiting, gagging and trouble sleeping. He also couldn’t eat random foods and took eons longer to tolerate normal food than other children his age. Take peaches for example. They made him vomit, so we just avoided peaches.  One time I made homemade veggie soup and pureed it for him to have in a pouch. I felt like a champion mother! Right? Wrong- He vomited. We all just thought he was getting sick and we made some jokes about my cooking, but he was fine the next day. I know that he reacted to something in the soup. It wasn’t my cooking. It was FPIES. He outgrew it around 1 and a half, but is occasionally sent home from preschool for unexplained vomiting that has not always been related to a stomach virus. How did we know? Nobody else ever got the virus, including children in his classroom. Even though he has largely outgrown this disease he still has strange stomach pains and symptoms that no one can explain-including an irrational fear of food.  

The most reputable organization that is supporting FPIES research the International FPIES Association. I am raising money for them because their work directly supports medical research to advance our understanding of FPIES. 

On Sunday, July 28, from 3-5pm my family and I are hosting a fundraiser walk at Country Park in Greensboro, N.C. We invite everyone to come rally around our children and other FPIES families to raise money to fight this disease. 

To join the walk, we have a suggested donation of $25 per person but any donation amount is greatly appreciated. If all you can donate is a hug, you are most welcome too. Wear teal to show your support of children with FPIES, or better yet, purchase an FPIES t-shirt for the event. I’ll share links as soon as the design is finalized. 

I will have a drawing for one of my oil paintings and donate the money to the cause as well. Drawing tickets are $5 each. You do not have to be present to win, but you do need to be able to pick up the painting within a week after the event. 

“Maybe she will grow out of it” just isn’t good enough for these children. Let’s do something about that. Let’s fund the research right now.

Monday, February 18, 2019

Summer Art Camp 2019

Come have some summer fun with me! To register your child or for any questions, text me or call at 912-704-3637. You may also email me at Please give your child's name and grade, plus your cell phone number and email address so that I can send reminders. I also need to know about any allergies. Class sizes are limited. Full payment reserves your child’s spot in art camp. Checks may be made to Katie Podracky. All camps are held at my home on Wednesday and Thursday mornings and all art supplies are included.

Up your Colored Pencil Game July 10 & 11 (rising 3rd grade and up)
9 a.m.-12 p.m.
Would you like to know how to make your drawings pop with color? Join me and use my Prismacolor stash to learn how to shade and layer with the softest prettiest colored pencils around. Subject matter is up to you, but I will have examples to choose from. This class focuses on shading and color theory.

Under the Sea Paper Collage July 31 and Aug. 1 (rising 2nd grade and up)
9:30 a.m.-12:30 p.m.  (time is different for this camp due to my childcare)
Baby SHARK DO DO DO DO DO DOOO. First we channel our inner sailor while painting splashy watercolor techniques on paper. (and tempera, oil pastel & acrylic paint too) Then we will use the paper to collage an underwater seascape complete with sharks, sunken ships, coral reefs, clown fish, sea turtles, anemones, mermaids, Davie Jones and anything else campers fancy. This is one of my favorite camps.

Paint the Eiffel Tower (or a Parisian portrait of your pet- I'm serious!) August 7 & 8 (rising 2nd grade and up)
9 a.m.-12 p.m.
Let’s pretend we’re in the city of light while we paint bistros, flower markets, French bulldogs carrying baguettes and the Eiffel tower! Of course we will have to nosh on French macaroons…and coffee- well maybe just for the teacher. (wink)

Crepe Paper Flower Bouquets August 14 & 15 (rising 4th grade and up)
9 a.m.-12 p.m.
Sculpting paper flowers takes patience and love, but boy are they beautiful when you’re finished. They’re also the perfect gift for mamas everywhere (and they last). We will create one bouquet per student for a really special summertime memento. This is not an easy peasy project. Determination and attention span are a must, but if you’ve got those, come on over and work on that hand-eye coordination with me to make a one of a kind bouquet.

Wednesday, November 28, 2018

Society 6

My whimsical watercolors are finally available for purchase in all kinds of products. Think phone cases, art prints, book bags, stainless steel tumblers, throw pillows, canvas bags, totes and even side tables. Here are some images showing the detail and quality of a few pieces. I'm really happy that I went with Society 6 to produce these-- they are quality. The awesome photographs were taken by my friends at Blue House Photography. (Thanks Al and Rachel!)

Check it out here at Society 6 and be sure to search for "katiewallart" if you have any trouble finding me.

Friday, August 24, 2018

Art Lessons with Katie Podracky Fall 2018

All art lessons are Thursdays from 2:45-3:45 at my home. (message me for the address please)

To pay in advance, it will be $165 for 11 lessons Sept-Dec, due at the time of your first class. If you know you won’t be able to make a certain date, please go ahead and subtract $15 from the payment and let me know when your child will miss. Feel free to share this information with any other students who would like to join us. I have a limit of 10 students, and many of the spots are already spoken for.

Thursdays 2:45-3:45p.m. $15/class 

Hot Air Balloon session
Sept. 13- Begin hot air balloon watercolor paintings with collage
Sept. 20- Continue hot air balloons (make background)
Sept. 27- Continue hot air balloons (collage)
Oct. 4 Finish up hot air balloons and do mini project as time permits

Fall Ceramic Plates and Halloween session
Oct. 11 Begin thankful plates (Design, draw and glaze fall themed ceramic plates that will be ready for Thanksgiving.)
Oct. 18 Continue glazing plates
Oct. 25 Halloween mini project and finish plates if necessary

Holiday Clay and Paint session
Nov. 1 Clay Day! Sculpt Ceramic Christmas Trees with a coil method
Nov. 29 Begin holiday painting (The Nutcracker theme)
Dec. 6 Continue holiday painting and glaze Christmas Trees
Dec. 13 Finish holiday paintings and take home Christmas tree

Thursday, March 15, 2018

Summer Art Camps 2018

It's time for summer art camps again!  Here they are. To register your child, contact me by text, phone or email.  If you're new and don't have my contact information, leave me a message via my website ( or find me on Facebook and I'll be glad to add your little one! Please give your child's name and grade, plus your cell phone number and email address so that I can send reminders.  I also need to know about any allergies. Class sizes are limited and first come, first serve. Full payment reserves your child’s spot in art camp. Checks may be made to Katie Podracky.

Clay Days
July 11 & 12 AND a glazing day (Aug 1 or 2) (rising 2nd-6th) 9 a.m.-12 p.m.
During the first two days of camp, we will experiment with slab building techniques and campers can choose to work on animal pinch pots, coil pots or their own clay idea creations. The pottery wheel will be available for experimentation as well. All clay pieces will be fired and campers return for one glazing day (9-12 am), on a day that fits their schedule. (August 1or 2 are scheduled glaze day options, but I can open some days in late July to meet everyone’s needs too).

Watercolor Seascapes  
August 8 & 9  (rising 2nd-6th) 9 a.m.-12 p.m.
Back by popular demand, this project features beautiful splashy watercolor techniques on paper. We use the paper to collage a seascape complete with boats, corals, mermaids and anything else campers fancy. The art will be frame worthy! This is one of my favorite camps.

Paint a Saltwater Marsh
August 15 & 16  (rising 3nd-7th) 9 a.m.-12 p.m.
I’ll teach some of my favorite underpainting methods and show you how to make your very own saltwater marsh scene with layers of paint and LOTS of color. This is the “fine art” version of summer camps where we paint on canvas like professional artists.  Please wear old clothes that can get stained.

Batik Scarf
August 22 & 23 (rising 3nd-7th) 9 a.m.-12 p.m.
In this camp, we will create a beautiful scarf using methods of batik wax resist and fabric dyeing. Scarves can be worn, of course, or they can be used to wrap a special gift, to frame as art, or as a fun part of your next interpretive dance routine!

September 13th:  Small group art lessons begin on Thursdays from 2:45-3:45 p.m. (rising 2nd-5th grades)

$15/ class. Limit of 10 students