August is Psoriasis Action Month and it should come as no surprise that I have been living with psoriasis for about 20 years and share all about my journey, the highs and lows on Instagram and Instagram stories. But the main thing is to make sure we are taking action every day/week/month to do manage your psoriatic disease.
Ways To Take Action
AC*TION // the fact or process of doing something, typically to achieve an aim
the fact or process of doing something, typically to achieve an aim
For Psoriasis Action, the National Psoriasis Foundation wants YOU to take action to manage your disease. Whether it be going to the appropriate doctor, evaluating whether or not a treatment is working, or gaining more knowledge about psoriasis – take action today.
Here are some ways to take action when living with psoriasis. Also, even if you don’t have psoriasis, these are some really cool ways to learn more about those of us living with psoriasis. Because chances are that you know someone who does live with psoriasis.
Facebook and Twitter
It’s Psoriasis Action Month. Did you know that psoriasis impacts more than 8 million Americans? Good thing there are many safe and effective treatment options available. Do you know what’s available to help you? Find out with this quiz from the @National.Psoriasis.Foundation. http://bit.ly/PsO-Action-Month
Instagram + Instagram Giveaway
Make sure to follow the National Psoriasis Foundation on Instagram because for the month of August they are running a contest where you can win some REALLY COOL PRIZES! They also have a quiz on Facebook and Twitter for people to lear more about treating their psoriasis.
More About Psoriasis from the National Psoriasis Foundation
Psoriasis is a debilitating disease that impacts more than 8 million Americans and 125 million people worldwide. The good news is that today there are more safe and effective treatment options than ever before.
But what works for one person may not work for another and once you find a treatment that works, it may lose effectiveness over time. That’s why it’s important to stay up-to-date on the latest treatment information.
The National Psoriasis Foundation helps educate people with psoriasis and encourages them to assess their treatment options and discover what’s possible through the right treatment.
I also have a Psoriasis Highlights on my Instagram that you can follow along my journey with some product highlights, fashion tips, my medication, and much more.
Thanks for stopping by! If you have psoriasis let me know below so we can connect, I’m always interested in meeting new people so we can do this psoriasis journey together! If you don’t have psoriasis and you’re here, leave a comment below as to how you found me 🙂
11 Comments
Elena tabler
October 12, 2019 at 4:32 amHi there I ran across your blog about psoriasis, I am afraid to say I am affected by this immune deficiency also. It started on one knee a patch went away and came back with a vengeance. Now its everywhere and I do mean everywhere the lotions sink in my skin and dont work I’m constantly applying stuff its itchy it has affected me by not letting me enjoy my life with anyone no intimacy at all…it pokes me at times on the back of my legs while I’m driving I get to finally see a doctor on October 25th. I cant wear cute clothes I just bought a tanning canopy but afraid I might over do it.. please give me tips I will accept just a minute of your time if it means I dont feel so alone in this fighting lifelong journey
SabrinaDSkiles
December 3, 2019 at 4:22 pmHi Elena – I’m glad you found me! I’ll send you an email. Please always feel free to reach out to me via email as well at homegrownhoustonblog@gmail.com
SabrinaDSkiles
March 3, 2020 at 5:59 pmI’m glad you found me, I just sent you an email!
Kim Martin
January 29, 2020 at 6:36 pmMy first outbreak was in May 2018 and it has been a nightmare ever since. For most of the time it has been isolated to my scalp, ear and forehead. It has been so bad over the past 5 months that I have lost a ton of hair…A concerning amount of hair actually. It has now progressed to my breasts, my forearms and a few small patches on my legs.
I have tried a ton of topical medications, natural remedies, stress reduction and it has not helped. This has taken such a huge toll on my mental health as well. My insurance recently approved Otezla and I started it 6 days ago. The side effects suck but I’m hoping it will help. Any suggestions would be welcome! I’m just happy to connect with others who are having a hard time with this chronic condition.
SabrinaDSkiles
February 10, 2020 at 5:11 pmI’m glad you found me! Please send me an email at skiles.sabrina@gmail.com and I’d love to talk to you so more!
Joseph Hooser
February 26, 2020 at 1:17 amHe I’ve had psoriasis for 25yrs I’ve been through multiple treatments from methotrexate to humara to otezla, not including the thousands of topicals I’ve tried n naturals! Nothing seems to ever work I’m tired of fighting it any suggestions would be greatly appreciated thanks
SabrinaDSkiles
March 3, 2020 at 6:04 pmI am literally right there with you. I have tried everything you mentioned too. Unfortunately, psoriasis is a chronic condition, meaning “life-long”. There still is no cure for it, so right now we can learn how to manage symptoms. Combination therapy (a combination of different medications) might be an option for you. Talk to your derm and see what they say. Email me if you need anything else, it’s homegrownhoustonblog@gmail.com. I’m so glad you found me!
Shahib
February 29, 2020 at 6:14 pmHi I have psoriasis, been living with it since I was around 5years old, well that’s what my mum and dad tell me, I’m 33 yrs old now, need help, advice and guidance, just had my 1st flare up. HELP!!!!!
SabrinaDSkiles
March 3, 2020 at 6:02 pmLet me know what I can help you with, I just sent you an email!
Kristi Thomson
March 20, 2020 at 8:41 amSo glad I found your blog. I am 69 years old and have had psoriasis for about 10 years. I am just now learning about the fact that arthritis can accompany psoriasis. Can you guide me to good sites about psoiriatic arthritis? Thanks!
SabrinaDSkiles
March 20, 2020 at 5:21 pmHi Kristi, glad you’re here! Make sure to check out the National Psoriasis Foundation, they have a lot of great resources. Also check out Julie Cerrone of It’s Just A Bad Day, Not Life. She has been living with PSA for a long time, is the WEGO Health Patient Advocate Director and has her own blog talking about her PSA journey. I hope this is helpful! Feel free to email me at homegrownhoustonblog@gmail.com