Categories
It's Just A Bad Day Pregnancy PsA

4 Pregnancies With Psoriatic Arthritis

I specifically remember at the height of my disability leave, laying in bed thinking to myself, “will I ever have a family?”. I remember thinking, my body can barely function on its own right now – how could it ever support growing life and then take care of it?

This moment is one I think of alot – especially when laying in bed at night after I put the kids down for bed.

As I’m in the home stretch of my FOURTH pregnancy now, it’s surreal to me what my body has done. It has grown life four times and not only sustained me, but helped me flourish myself.

Over the years my psoriatic arthritis has had ups and downs. Of course, I’ve had flare-ups here and there. But when I look back over the last 5-6 years (my “pregnancy era”) I have to say that it’s been fairly well controlled.

When I reflect on what I’ve learned over the years, a few things stand out:

Know Your Triggers AND Your Boundaries

Prior to becoming pregnant my first time, I did A LOT (I mean, A LOT) of work to identify my specific triggers for my arthritis. I found out that many foods that I was eating contributed to inflammation and fatigue in my body. I realized many of the products (soaps, beauty products, candles, etc) I was using also contributed to symptoms. I went through an entire exercise of revamping my diet and lifestyle – and every ounce of it was worth it.

I kept a SUPER strict diet. I stayed away from every single trigger I could and refused to budge. BUT, once I started having kids I realized what I had created was unsustainable for a busy mom.

So I started exploring my boundaries with my triggers. For instance, grains are something that cause me fatigue. Before I became a mom, I avoided them at all costs. I never ate them. BUT, once I became pregnant and started throwing up 3-4 times a day, I realized I needed rice and other non-gluten-free grains to keep me going throughout the day. I will admit there were MANY times that I ate it too much and then paid the consequences (achy joints, fatigue, etc). But I didn’t necessarily have a choice. I HAD to eat SOMETHING.

Over the years I’ve incorporated a little bit of these things back into my diet- but I’ve come to realize how much I can eat and where my limit is.

Have Patience With Yourself

You can’t do it all, nor should you. And you can’t do it alone.

Before, when I was not pregnant, it was hard enough to manage my psoriatic arthritis. But now, add in a growing baby and it makes it even harder.

If your body tells you to rest. REST.

If you need help, ask for help.

You’re not only just taking care of you now, but your baby.

Every Pregnancy is Different

Through my years of talking about psoriatic arthritis online, I’ve encountered countless women who have gone through pregnancy as well. And what I can tell you is that everybody has a different experience. And even every person can have a different experience pregnancy to pregnancy.

Each of my pregnancies has been totally different.

For my first, I broke out in the most psoriasis I’ve ever had. With my second, my joints ached a lot (but I went into that pregnancy with my symptoms flaring more than the others).

And with my 3rd and 4th, the only times I’ve had problems was when I ate trigger foods that I know always bother me.

The only thing I can gleam from my experience is I think it depended on how well controlled my PsA was going into the pregnancy. Like I mentioned about, with my second going into it I was having a lot of symptoms. And that seemed to be the pregnancy that I had the most joint pain. Coincidence? Maybe? It was also 2020, so there were LOTS of emotions running wild there. I’ll probably never know, but the thing I can take away is that each one was definitely different in their own ways.

There Are Medication Options Out There

When I was pregnant with my first, I wrestled a lot with what if I needed to be on medication while I was pregnant or breastfeeding. I remember worrying SO much about it. Probably worrying too much.

But now, 6 years later from my first pregnancy- I can’t tell you the countless friends I know who have been on medications through their pregnancies or postpartum and have had totally healthy babies.

With my second, I had a tremendously productive conversation with a maternal fetal medicine doctor about the risks vs rewards of taking medication during pregnancy. I ultimately didn’t end up taking any medications during any of my pregnancies, but the conversation I had with him made me feel so hopeful that if I DID need to I had someone on my side who would help me make the right choice.

When I was pregnant with my 1st, I was on Otezla at the time. It honestly was only helping me about 50% so I decided to stop it (of course with consult from my doctor). But, since I had been taking it in the beginning, I did sign up for a Mother to Baby study to share my data with others. I’m so glad I did that because it made me feel like I at least contributed to helping some other mother in the future find piece of mind.

I know it can be unnerving, but absolutely talk to your doctor about your situation and what might be out there for you! There are lots of options.

Trust Your Body

And last, but certainly not least, might be the hardest one for someone with an autoimmune condition.

Trust. Trust your body.

With an unpredictable condition like psoriatic arthritis, it can be really hard to trust in our bodies. With the aching joints, flaring skin, debilitating fatigue- many of us start to lose that trust.

But with pregnancy, you have the ability to take someone beautiful and learn how amazing your body CAN be. Despite any hardships you may have encountered with your PsA – your body can grow a human AND birth that human. WHAT?! THAT IS WILD TO ME. I honestly find this so fascinating.

With each of my pregnancies I’ve been super sick through most of it. Throwing up just becomes a way of life that honestly sucks.

BUT, the one thing I know in the back of my mind is – this will end. Pregnancy will end. It will end one way or another. Unlike PsA, when I can be in the thick of it and find it hard to see there is a light at the end of the tunnel.

Pregnancy gives us the chance to reconnect with our bodies and to start to build some trust back with it. And honestly, building that trust through pregnancy and then taking it back into every day life to manage PsA can be transformational. So please don’t discount this opportunity you have during pregnancy.

My One Piece Of Advice

So these are my main takeaways. At the end of the day, we’ll all have different experiences with psoriatic arthritis and pregnancy. If I could offer you one suggestion or one piece of advice, let it be this. . .

If having a family is something you want and you’re currently in the midst of a flare that makes you think you’ll never have that. Don’t give up hope. NEVER in a million years did I think I’d have 4 kids. Especially the version of myself when I was on disability – she NEVER EVER would have believed that. But here I am, 10 years later, 4 pregnancies later, and have a beautiful family that I’m so grateful for.

Just remember – it’s just a bad day, NOT a bad life. Don’t ever let a diagnosis hold you back from living the life you want or deserve. Sure, maybe you have to make some accommodations and modifications along the way – but you can have it all.

Wishing You A Pain Free Day!

Julie Croner, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
It's Just A Bad Day

Find Your Yes: Arthritis Resources

This blog post was created in partnership with The Arthritis Foundation. I was compensated for my time, but I can assure you I wouldn’t pass along this information if I didn’t feel it was valuable to the arthritis community as a whole. 

As an adult, I can look back and think of many times that my parents were right and I was clearly wrong. It’s something that we can joke about now, but in the moment would cause frustration.

Of course, as a teen, I didn’t understand why I couldn’t go to a friend’s house if their parents weren’t home or why I wasn’t allowed to take the car and drive to a different state by myself. 

But one thing that really sticks out in my mind are the fights that I had with my mom about having arthritis.

No Title

No Description

I honestly remember sitting in the bathroom with the door locked, crying my eyes out because my mom told me I had to go get an MRI with contrast the following day. The MRI part wasn’t the part that upset me, it was the contrast part. I knew they’d have to inject me with dye and to a young kid that was going to hurt!

I can’t even imagine how my mom was feeling sitting on the other side of the door hearing me cry and scream about it. 

You see, when I was in middle school a rheumatologist told me they thought I had psoriatic arthritis. But, since there weren’t any specific tests to pinpoint exactly if that’s what it was, the diagnosis wasn’t ever “official” on my medical file.

I wasn’t even through puberty yet, so in my brain, there was NO way I had arthritis. I WASN’T A GRANDMA! 

My knee(s) would flare up, I’d be achy, I’d have some symptoms – and my mom would bring up the arthritis diagnosis and I’d dismiss it. I remember screaming so many times to my Mom (sorry Mom) that I didn’t have arthritis. 

This went on even into my 20’s! I remember being a 26-year-old working on a project for work in Chattanooga, TN. I was sitting in the kitchen at my client’s site, talking to my mom on the phone during lunch. I was calling to tell her that my orthopedist wanted me to go get an MRI on my knee because it was acting up again.

“It’s probably your arthritis!” I remember her saying. And again, I got mad because I wasn’t a Grandma. I COULDN’T POSSIBLY have arthritis.

But guess what – in America, there are 54 MILLION Americans with arthritis. And arthritis isn’t just an “elderly disease.” Two-thirds of people with arthritis are under the age of 65, including 300,000 children.

And I was one of those children. . . even though I didn’t FULLY embrace the psoriatic arthritis “official” diagnosis until I was 27, laying in a hospital bed the week of Christmas in so much pain I didn’t know what to do. 

Candidly, it took me a while to get a grip on what the diagnosis meant and how it would change my life. I spent a good 6 months in bed, depressed, not wanting to move, in denial. 

But then, I had my ‘aha’ moment. It was in connecting with other patients online that I realized I wasn’t alone and I didn’t have to live a life of misery. In fact, I could still live an awesome life DESPITE psoriatic arthritis. 

In 2013, I decided to start my blog and start advocating for my condition. One of the first places I went was to the Arthritis Foundation. Getting involved in the local Pittsburgh chapter of the Arthritis Foundation was so refreshing and inspiring. That first year I joined local patients and caregivers and went to Harrisburg to advocate for change. After that experience, I joined the Advocacy and Mission Committee for Arthritis Foundation and had a blast going to state senator and representatives offices. I volunteered for the Jingle Bell Run and the Walk to Cure Arthritis.

The Arthritis Foundation is the Champion of Yes.

Leading the fight for the arthritis community, the Arthritis Foundation helps conquer everyday battles through life-changing information and resources, access to optimal care, advancements in science, and community connections. Their goal is to chart a winning course, guiding families in developing personalized plans for living a full life – and making each day another stride towards a cure. And that’s what they did for me!

Now I will say, The Arthritis Foundation has changed over the last few years in a GREAT way! When I first started, there weren’t as many resources for psoriatic arthritis. But now, that’s not the case at ALL! 

They’ve also launched their Live Yes! Arthritis Network which provides personalized help and support to adults living with all types of arthritis and rheumatic conditions and parents or guardians of children living with arthritis. Their programs offer opportunities for connection, education and empowerment via Live Yes! Connect Groups, Online Community and conferences.

If you’re looking to get involved I’d suggest you check out one (or all) of the 3 following focuses within the Live Yes! Network:


The Live Yes! INSIGHTS is going to change the future of arthritis forever. By asking those affected by Arthritis to take a 10-minute assessment where they will share their overall arthritis experience – answering questions relating to their symptoms, pain levels and how arthritis affects their function and mobility – the Arthritis Foundation gets a better sense of what people experience on a daily basis.

The data they collect will then show decision-makers the realities of living with arthritis – ultimately paving the way for change by breaking down barriers to care, accelerating research and creating resources that will make a difference in people’s lives. Click here to learn more about Live Yes! Insights. 


The Arthritis Foundation’s in-person, peer-led Live Yes! Connect Groups are not your typical arthritis “support groups.” They are an in-person way (though not in-person right now) to bring adults with all types of arthritis and rheumatic diseases together for fun, social and informative educational events and activities focused on mutual support and positive coping strategies for living well. To learn more and find a group near you, click here.


The Live Yes! Online Community allows adults with all types of arthritis and rheumatic diseases to chat 24/7 about what matters most, including medical issues, frustrations, tips, life hacks and more. To learn more, click here.


I’ve found the Arthritis Foundation resources invaluable and I hope you will too!

If you’re someone who is impacted by autoimmune arthritis, I suggest you check out these tremendous programs. I know they’re a wonderful resource to the community and I hope you all take advantage of the programs they have to offer!

Also, in these times of COVID-19, the Arthritis Foundation has been working to keep the arthritis community safe and up-to-date with reliable and trustworthy information and tips on how to stay healthy, as it’s more important now than ever. For more information, click here.

Wishing You A Pain Free Day!

Julie Cerrone Croner, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune It's Just A Bad Day Pregnancy PsA

Does Psoriatic Arthritis Prepare You For Pregnancy?

Man, it’s crazy how fast a year goes! Last year this time I started having contractions and was thinking my little one would be here any day. Well, let me tell you – February 22nd to March 17th was a LONG ASS TIME. It may have only been a few short weeks, but to me, it seemed like eternity.

Looking back, my pregnancy taught me a lot, but I also had a lot of preparation for my pregnancy that I didn’t even realize!

Because I’ve lived with a chronic illness for several years now, there are certain things that I’ve grown accustomed to. Fatigue, pain, pacing myself, canceling plans, a strict diet — these are all are normal to me.

Little did I know all this would prepare me for one of life’s momentous experiences.

I ended up realizing there were 5 ways that having a chronic condition, like psoriatic arthritis, prepared me to go through the amazing journey of pregnancy!

 

https://www.healthcentral.com/article/does-living-with-chronic-illness-prepare-you-for-pregnancy?ap=423

Check out the article and let me know what you think.

 

Do YOU think chronic illness prepares you for pregnancy?

 

Wishing You A Pain Free Day!

Julie Cerrone Croner, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune Diet It's Just A Bad Day PsA

Managing Weight & Psoriatic Arthritis

When it comes to psoriatic arthritis, managing your weight can have significant impacts on your overall health. As reported by the National Psoriasis Foundation, weight loss in conjunction with certain medications can together help improve your symptoms. Carrying less weight will help lessen the burden on your joints and can potentially give you more energy.

However, managing your weight with psoriatic arthritis is difficult. Your joints are achy and swollen. You’re low on energy. And your whole body is inflamed. Conditions aren’t always conducive for a two-mile jog!

Whenever I have a psoriatic arthritis flare, I find myself gaining weight from lack of activity, side effects from medications, and the inflammation all throughout my body.

While we each may have different reasons we’ve gained the weight, I have detailed out my seven tips on ways to manage weight while thriving with your psoriatic arthritis.

Click to read and make sure to share after reading!

https://www.healthcentral.com/article/tips-for-managing-weight-gain-with-psoriatic-arthritis/?ap=423

Do you have tips? Let me know in the comments below! I’d love to hear them.

 

Wishing You A Pain Free Day!

Julie Cerrone Croner, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune PsA

Getting The Support You Need

Having a chronic condition can be extremely tough. There are ways that you may be hurting that other’s can’t completely understand.

You can try to explain it, but so many times you can’t understand it unless you’re living with it. Which can be so frustrating!

Here are 2 articles that I wrote for you that may help.

This first one would be a great one to share with others. Let them know if certain parts resonate with you! And if there are things you’d add, make sure to tell them!

https://www.healthcentral.com/article/5-ways-im-suffering-and-youd-never-know/?ap=423

 

This next one is a great resource for you to arm yourself with tools to get others to help you. Asking for help is NOT a form a weakness. On the contrary, asking for help is knowing your limits and knowing that you can’t do EVERYTHING yourself.

https://www.healthcentral.com/slideshow/10-tips-to-get-the-support-you-need-with-your-chronic-condition?ap=423

We must learn to educate others and ask for help. This may sound crazy, but the people in our lives can’t read out minds! We must speak up and let them know how we’re feeling and what we need.

I hope these two resources can help you! Do you have any suggestions on getting the support you need for your chronic illness? Let me know in the comments below.

Wishing You A Pain Free Day!

Julie Cerrone, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune Humira It's Just A Bad Day Medication Otezla PsA Treatments

Psoriatic Arthritis And Biologics. What You Should Know.

Back in middle school, my doctors didn’t want to put me on “heavy duty meds” because I hadn’t even gone through puberty. And, come to think of it, it was the mid 90’s so biologics were probably not indicated for juvenile use yet.

In 2012, when I did start on them, I wanted everything and ANYTHING that would help me. I didn’t weigh my options or list the pros and cons. I heard that it could help me and I was like “sign me up”!

But now, I have a much different thought process. YES – they help. YES- they can be life-changing. BUT, do I want to take them?

There’s so much to consider when deciding to go on a biologic. I’ve written a few posts that I’d love to share with you that can help you make an informed decision.

First, I wrote this post about the different types of biologics and biosimilars that are approved for psoriatic arthritis (as of the date of publishing).

https://www.healthcentral.com/article/biologics-and-biosimilars-for-psoriatic-arthritis?ap=423

Second, I’d love to share with you several patient’s thoughts on what they’d wish they’d have known before starting a biologic.

https://www.healthcentral.com/article/what-i-wish-id-known-before-starting-a-biologic?ap=423

And third, I’d like to share 3 success stories with you. Biologics can be life-changing and can really help you manage your conditions. Don’t take my word for it, take these 3 ladies words for it!

 

https://www.healthcentral.com/article/amberlees-psoriatic-arthritis-journey-with-biologics?ap=423

https://www.healthcentral.com/article/michelles-psoriatic-arthritis-biologics-success-story/?ap=423

https://www.healthcentral.com/article/pso-psa-success-story-jen-fisch/?ap=423

I’m currently not on a biologic, but my latest course of treatment was Otezla. If you’re interested in my experience, click here to find posts about it!

I personally find that a 5 step approach to my psoriatic arthritis helps me manage my condition. To learn more about it, check out this post and follow the steps (Elimination DietSupplementsToxinsMeditation & Mindfulness, and Yoga & Movement).

Wishing You A Pain Free Day

Julie Cerrone, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune PsA

Does Psoriatic Arthritis Get Enough Attention?

How I was feeling about my immune system during my psoriatic arthritis flare up | itsjustabadday.com Julie Cerrone Certified holistic health coach, spoonie blogger, autoimmune warrior, yoga instructorNO.

HELL NO.

PSORIATIC ARTHRITIS DOESN’T GET ENOUGH ATTENTION.

AND YES, IT PISSES ME OFF. (HENCE THE ALL CAPS)

Back in middle school when a doctor mentioned it, my family and I had NO idea what it meant.

In 2012, when I was “officially” diagnosed with it…. we still had no idea what it meant. All we knew was that golfer guy had it since we saw him talking about Enbrel on TV all the time.

Sure, you could say – well Julie. Just because you didn’t know about it doesn’t mean it doesn’t get enough attention. And that’s fair. Whenever you’re not thinking about something consistently, you don’t necessarily notice all the places it pops up.

But having been paying attention for a few years now, I can tell you it doesn’t get enough attention. RECENTLY, in the last year or so, there has definitely been a push for more awareness. Before, the Arthritis Foundation rarely mentioned it! Now they have their own PsA publication (which is great!). There was even a commercial on tv JUST for psoriatic arthritis that ran this last year. And more and more pharma commercials are poppin’ up about it as well.

So there is a shift being made. . . but there still needs to be more awareness. And because of this, it drove me to write the following article.

My ask to you is to read it and then share this post so that others realize that we need to bring more attention to this condition. No, it’s not rheumatoid arthritis. No, it’s not just psoriasis. Psoriatic arthritis is it’s own thing and DESERVES attention on it’s own as well.

My Health Story

Ovarian Cancer Prostate Cancer Macular Degeneration High Cholesterol Hair Loss Bipolar Disorder Breast Cancer Psoriatic Arthritis Hepatitis C Hypertension COPD Celebrity Health & Wellness IBS Hypothyroidism Ulcerative Colitis Exocrine Pancreatic Insufficiency Parkinson’s Disease Ankylosing Spondylitis ADHD HIV/AIDS Asthma Psoriasis Heart Failure Anxiety Disorders Stress Migraine Menopause Type 2 Diabetes Rheumatoid Arthritis Lung Cancer Eczema Endometriosis Multiple Sclerosis Weight Loss Atrial Fibrillation Alzheimer’s Disease Crohn’s Disease

What do you think? I’d love to know your comments below!!

Wishing You A Pain Free Day!

Julie Cerrone, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune AVN It's Just A Bad Day Personal Victories PsA Regenexx Travel

5 Take Aways From Conquering Personal Challenges

Traveling has always been one of my favorite things to do.

Ever since I was young, I’ve always enjoyed seeing new places, cultures, and things. From exploring America, laying on the beaches of the Caribbean, safari-ing (is that even a word?) through the African bush, riding camels on a Tunisian beach with Arabic speaking natives, eating my way through Europe or whatever other trips I can find myself on – I’ve always had a wander lustful heart. I always tried to soak up every moment and never knowingly took the situations for granted.

Having my mobility taken away from me for 3.5 years made me look at things in a different light.

When it first all happened, I had panic attacks so bad I didn’t want to travel. Actually, a trip that I took with my family to Florida in the Summer of 2013 ended up being one of the major points during my healing journey – but I didn’t want to go. I just wanted to lay in bed, not leaving my house, and do nothing.

It was during that trip I had the realization that I still could live an awesome life – despite any obstacle that was presented in my way.

Obstacle: Psoriatic arthritis?

Solution: Pacing myself and planning ahead.

 

Obstacle: Avascular Necrosis (aka why I was on crutches)?

Solution: Planning ahead, renting wheelchairs, and asking for help

 

The first few trips I took were sobering. I didn’t have the stamina that I had before (my 2012 flare up + disability leave) and had to rest a lot.

I remember going on a trip with my boyfriend at the time and I so badly wanted to keep up with him and his sister’s family. I was in a lot of pain, tired, and would call it a day fairly early. I had never been like that and it was something I wasn’t used to while traveling. That trip, albeit a great one, was a wake-up call to me that things may never be as they were before.

As the years went on, I got more comfortable with traveling. (I’ve detailed some of those trips – like this one comparing trips to San Fransisco and this one about a trip to NYC)

I had my airport routine down pat. (READ: Traveling with disabilities lesson’s learned)

I’d have someone drop me off, I’d check my bag so I wouldn’t have to worry about it, get a wheelchair and be wheeled straight to my gate. Someone would help me on the flight, they’d pick me up at my destination and then either take me to my next flight or take me to baggage claim to get my bag. Once I had my bag, I’d either get them to help me in a cab or go rent a car.

After a while, this routine seemed perfectly normal. To me, dragging my bag behind my crutches didn’t seem like such a big deal at all! I still didn’t have the stamina to walk around or be as active as I’d like – but at least I was confident in going places myself.

When I went out to Colorado to have my stem cell procedure done, I was so bummed because the atmosphere out there was SO active. I wanted to go hiking or biking or walk up to see beautiful views on the top of mountains. And to an extent, I did! I crutched over little rocks and wiggled my way to the top of more easily accessible viewpoints. And it was beautiful! I told myself that I’d be back and next time I’d be back to do all the active activities.

Since my stem cell procedure, I’ve gone on many trips. Mostly for work or advocacy things, but sneaking in a vacation here or there (like this one). But during my trips, I still paced myself. I didn’t walk as much as I wanted to and made sure to take care of me. It was always at the top of my mind.

But at the end of May/beginning of June 2017, my family went on the trip of a lifetime – 12 days to explore 3 of the 8 Hawaiian islands.

 

We made it to Hawaii 🙂 #FamilyVacation

 

Up to this point, every trip I had gone on I’d have a twinge of fear that I wouldn’t be able to keep up or do the things I wanted to. But to be honest, that thought never crossed my mind going to Hawaii. I was so excited to see everything.

Every day for 2 months prior, I rode my desk bike hoping to build up my stamina to hike and see all the things I wanted to see. I knew I’d have to build myself up and then make sure to take care of myself when I was there.

My sister and I planned to make sure we had the right food to eat, I brought my Deep Blue, extra supplements and I brought pain pills just in case.

In Hawaii, we hiked up Diamond Head on Oahu, we hiked Waipi’o Valley (which is insane fyi), we hiked to see waterfalls, botanical gardens and more on the Big Island and in Maui, we hiked on the Road to Hana.

To a normally active person, these hikes may not have been a big deal.

But to me, they were hugeThis trip was the most active I’ve been in 5 years.

I remember the first time I walked on the beach after my stem cell procedure (read about it here) and to be hiking around Hawaii 2 years later was so amazing.

The significance of what I was doing was never lost on me the entire time we were there.

 

I swear the whole trip I just kept saying thank you, mahalo, thank you, mahalo, over and over and over again in my head.

I tried to soak up every moment that I could.

At the end of the day, there are a few things I’d like to leave my chronically fabulous friends with as takeaways from my health journey (thus far):

 

5 take aways from Conquering personal challenges - itsjustabadday.com Overcoming psoriatic arthritis challenges and obstacles on vacation

1) Just because you can’t do something now, doesn’t mean you won’t ever be able to do it again. 

As life goes on, our plans and goals adjust. The way we’re able to function and do things may need to be altered, but that doesn’t mean we can’t find SOME way to enjoy the things we used to love to do. Maybe it’s not today, but if it’s important to you, you can always find a way. If there’s a will, there’s a way.

 

2) Pace yourself and listen to your body.

I’m extremely fortunate to be able to walk again. I realize that some are not as lucky as I have been. But, just because I can walk doesn’t mean I can do ANYTHING I want. I still have to modify, I still have to pace myself. Sure, I hiked around the island, but I definitely had pain in the evenings. I doubled my turmeric every day and, eventually, I did end up taking pain pills in the evenings towards the end of the trip. It was a way for me to still enjoy everything I wanted to. There were a few times that I wanted to hike further, but I didn’t. (ok, so my parents forced me not too – but they were right and I was being stupid) We can still enjoy things, but need to PACE.

 

3) Plan ahead.

My sister and I always have to be careful of what we eat. So planning ahead, bringing food and knowing where I could go and get diet approved foods was really key for me. It helped me not stress out about it and made me feel comfortable.

 

4) Don’t be afraid to ask for help or support.

If you need help in the airport – ask for it! If you need to park in the handicap spot – don’t feel guilty! If you have to call it a night early, don’t feel bad doing so. You have to take care of you, first. Don’t worry about what others think – they don’t have to live in your body. YOU DO. Ask for help and take it.

 

5) Enjoy every little moment.

We take so much for granted. Things we wish we could do often cloud our minds. Instead, we need to focus on the things we CAN do and the things we’re grateful for. Make sure to remember this and try not to dwell on what’s lost or what can’t be. Focus on the here and now and what you can do. Embrace every moment the best you can.

 

RIP Pill-box 🙁

During the trip, I did leave something behind though that I am a little sad about.

I’ve had the same pill-box for the last 5 years. It’s seen me through some pretty rough times and it’s helped hold my supplements to get me better. The little compartments have been falling apart and I knew I needed to get a new one. Since we were going to be gone for 2 weeks, I knew I had to get another box anyway. I bought a new one, filled them both up and took them both to Hawaii. Once I took all the pills in my old one, I left it behind.

It’s weird, but I felt a little sad doing so because that pill-box has been a part of my health journey. BUT, if I had to leave it behind, it was a great place to do so. In a place that I had the opportunity to be active in!

All in all, this trip was the best trip I’ve ever taken in my life.

Mahalo to my parents, Mahalo to my body, Mahalo to life.

 

 

The amazing sites we saw, the experiences we had and the personal obstacles I overcame . . . this trip will be EXTREMELY hard to beat!

Have you gone on a vacation, or had an experience, where you overcame personal obstacles as well? I’d love to hear about them! Post about it in the comments below👇👇👇

Wishing You A Pain Free Day!

Julie Cerrone, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

 

 

 

 

 

 

 

 

Categories
Autoimmune Otezla PsA

Otezla: Week 3 Starter Pack Recap

Already finished up week 3 and headed into week 4!

Time flies when you’re having fun . . .  BAHAHA I can’t even type that with a straight face.

If you missed Day 0, Week 1 and Week 2 updates – catch up first!

Otherwise, check out my update and peep my lessons learned so far below.

 

One thing I completely forgot to say in the video was that the medicine has really been making me irritable. I can’t believe I forgot that part in there! I feel like I’ve been on edge and my poor family has been getting the brunt of it! haha

Notable for week 3:

  • Less headaches
  • Less stomachaches – with the exception of one bad day
  • Hands REALLY hurting
  • Still very bloated, gassy and going to the bathroom a lot
  • VERY irritable

 

Lessons learned so far:

  • MUST eat a substantial amount of food with the pill. I’ve found that eating and then waiting 30-45 minutes before taking the pill helps ease side effects
  • When I do have a headache, Doterra’s Past Tense helps ease it!
  • If you’re not taking a quality probiotic, you definitely should in order to support your GI tract. I take this one.
  • Celery juice is something I start my day with every day because of my psoriatic arthritis, but it’s especially important when taking this medication because it helps calm your GI tract.

I know that my doctor said being able to see the benefits from the medicine varies from patient to patient. Some realize the benefits right away, while it takes others a longer time to see. I definitely have not seen any relief so far- in fact, my hands have been worse the last week and a half. I don’t think it’s the medication’s fault, I think it’s just not giving me relief yet.

Maybe this week I’ll start to see results? Fingers crossed!

To read my Week 4 update, click here.

 

IMPORTANT NOTE: It is extremely important that if you experience side effects/adverse events from a medication that you report them. Why? Well, if you report them, more patients can be aware, drug companies can manufacture safer products and it can help the FDA do their job more appropriately. If you yourself experience adverse events, please make sure to report them to MedWatch.

 

Wishing You A Pain Free Day!

Julie Cerrone, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com

Categories
Autoimmune Otezla PsA

Otezla: Week 2 Starter Pack Recap

To recap thus far . . .

First, I freaked out and had to come to terms with taking Otezla. (Read: Am I a Failure? A Fraud?)

Then, after dragging my feet for a month, I finally decided to start it. (Peep: Starting Otezla)

Post week 1, I gave you an update on the side effects I was having. (Check out: Otezla: Week 1 Starter Pack Recap)

And now, I’m back with an update on how week 2 went.

Let’s just say week 2 was shitty . . . literally and figuratively.

 

 

I did have a pity party on Wednesday (halfway through the 2nd week) and the following rant ensued on Facebook. I found the comments from other patients very valuable. Definitely click on this post and see what other patients had to say about their Otezla side effects.

And while you’re at it, follow me on Facebook!

And then why not Instagram and Twitter (because they’re my favs and I’m on them the most!)

 

Julie Croner, It’s Just A Bad Day, Not A Bad Life

Sorry… this is definitely an UGH #WhatTheHealthcare rant . . . So I start #Otezla, right? And of course my insurance doesn’t cover it. In the interim, my doctor says to come get some sample packs…

Have you taken Otezla? What has your experience been? Write yours in the comments!

Click here to read my Week 3 recap.

 

IMPORTANT NOTE: It is extremely important that if you experience side effects/adverse events from a medication that you report them. Why? Well, if you report them, more patients can be aware, drug companies can manufacture safer products and it can help the FDA do their job more appropriately. If you yourself experience adverse events, please make sure to report them to MedWatch.

 

Wishing You A Pain Free Day!

Julie Cerrone, Certified Holistic Health Coach, Yoga Instructor, Patient Empowerer, Autoimmune Warrior (Psoriatic Arthritis), Avascular Necrosis, Complex Regional Pain Syndrome | itsjustabadday.com