About Me

Hi! And welcome to my page! I have been posting on this blog since 2010, six years of my life! I started my blog back when I was first diagnosed with Rheumatoid Arthritis and Lupus because I wanted to show that despite having these invisible illnesses, you could still live a life!

Since 2010, I have earned a master’s and a doctoral program. In those years, I wanted to share my life as a student, full-time employee, and wife. I wore many hats but through the years in school, my determination to succeed only grew. I graduated in May 2015 as Dr. Joanna Tucker. One of the biggest and best accomplishments of my life.

Since 2015 I have started my own Mary Kay business, which I love. I originally started my business to possibly start working from home. And then I succeeded in recieving access to the Publis Student Loan Forgiveness (PSLF) program. I will continue to work in public higher education for the next 9 years, and my loans after that time will be forgiven! I am so grateful because I do love what I do.

My Mary Kay business is a fabulous side business, I have some pretty amazing customers and I love getting my own products at a discount. I also enjoy growing in a new unit. My goals for this upcoming seminar year are to continue to grow to 100 customers.

I’ve debated for several months whether to keep this blog going since I’m not longer in school, I wasn’t sure what else I could offer. But then I realized, I miss this blog. I miss sharing my life and feelings to the great void. So I will continue to share my life, my thoughts, my dreams, my travels and my passions. I hope that someone out there enjoys it. My goal remains to share that despite having an invisible illness, you too can live a great life!

Dr. Joanna Tucker

34 thoughts on “About Me

  1. Hi 🙂 Totally love your point of view… I try hard to be positive with my illness ( I have Psoriatic Arthrtist and also have not been found to have a Rheumatoid factor in my blood. But My disease is so obvious (me knees swell up larger than canteloupes) and I’ve had it since I was 14 so I’ve been in the system for a while now despite having no official blood test stating I have RA or PA.

    I have been on methotrexate for 5 years and am adding on Arava starting this Monday since the methotrexate alone has completley failed me in recent months. Can you tell me a bit more about your first few weeks on arava … My wedding is in less than a month…but I want to start the meds so I will be at least on my feet during the festivities… will I have my hair? or should I start wig shopping? lol

  2. Thanks 🙂 I like the posh haircut… though she could do to smile a bit more 🙂 Unfortunately I already have very fine hair… so not a huge fan of the idea of it thinning! But like you said… gotta make the best of it! Thanks for giving me some insight… I’m starting it Monday … so here goes nothing!

  3. I want to say two things. One, I love your blog. I don’t have the same problem as you, I suffer from Fibromyalgia, Migraines, Depression, Panic Disorder, blah, blah , blah. Two, thank you for reading my blog and nominating me for a Sunshine Award. I am thrilled since I just started blogging and did not know if anyone would read my blog. Oh, three! I am not sure that this is ‘done’, but I nominated you. I know you have 2 already and so you don’t have to go through all those questions and answers again. I just hope to help others find your blog. Have a wonderful day!

    • Hey! I love your blog, definitely keep it up! I’m glad you like mine, I started just like you a little over a year ago! Fibro alone is a major battle to live with, we share that battle! And together we will fight it l, day by day!

      • Yes, it is a day by day thing. I had a good day yesterday and I’m having a good day today. I like to read about others’ thoughts on this disease as well as how they are continuing to live their lives as best they can.

  4. Hi!

    I am starting a directory of Bloggers who educate, support, enlighten, inform, inspire and motivate people about and with Fibromyalgia.

    I would really like to include you and your blog.

    Please have a look at the information for Bloggers on my site: http://fibromodem.wordpress.com/fck-directory/for-bloggers/; and, if you would like to be included, please follow the directions and then email me at fibromodem@hotmail.com.

    I hope you choose to be part of this new project.

    Regards,
    Fibromodem

  5. Pingback: Tomorrow is Rheumatoid Awareness Day. | Fibro Feist

  6. Hello! This post could not be written any better! Reading through this post reminds me of my previous room mate!
    He always kept talking about this. I will forward
    this write-up to him. Fairly certain he will have a good read.
    Thank you for sharing!

  7. I simply want to say I’m newbie to blogging and site-building and actually savored this web page. More than likely I’m going to bookmark your blog post . You definitely have impressive writings. Cheers for sharing with us your blog site.

  8. So appreciate what you’ve shared. I was diagnosed with RA 12 years ago, have had ups and downs, and now live med free. I’ve recently started blogging in the hope that I can help others as I share my healing journey with RA. Blessings!

  9. I have fibromyalgia. In reading your opening paragraph i had to chuckle. I have never heard of people with RA being called “squeakers” and people with fibro being called “spoonies”. Where did you come up with these “nick-names”? On another note, my goodness… you got a triple whammy! Since the symptoms of all three are similar how did your doctors figure out that they were separate?

    • 🙂 thanks! There is a great RA group called “squeaky joints” so the nick name became squeakers. And the spoonies came from the “Spoon Theory.” A great help for people with invisible diseases. Google it if you haven’t heard about it.

      In all honesty my rheumatologist hasn’t really figured out where the lines are. I started with RA and then when mtx didn’t work she did more blood work. That’s when she believed lupus come in, she switched me to a drug that worked for both lupus and RA and I began to improve. Six months later I was still in pain but it wasn’t in my joints. That’s when she started me on Lyrica for Fibro. And it helped so she has continued the treatment.

      Now she has me on everything she can for sjorgens disease. My eyes are the worst, but the Biotene and Bioten are helping.

      🙂 thanks for checking in! I love hearing from readers! 🙂

  10. Congratulations! I’ve nominated you for the Liebster Award! The Liebster Award is also known as the “favorite blog award”. And since your blog totally rocks my world, that’s why I chose yours. Check out my post to find out the steps to graciously accept your award, and keep up the great blogging! 🙂 Jenn xx

  11. Pingback: Unique leaves award | Fibro... Dealing and coping through laughter and tears

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s