Inclusion is Bliss

Inclusion is Bliss Inclusion is Bliss motivates you to live your best life, no matter your ability.

πŸŽ‰πŸŽ‰It’s Friday Friyay, y’all!πŸŽ‰πŸŽ‰Today I challenge you to get out of your own head. So many times we focus on all the thing...
09/19/2025

πŸŽ‰πŸŽ‰It’s Friday Friyay, y’all!πŸŽ‰πŸŽ‰

Today I challenge you to get out of your own head.

So many times we focus on all the things we are not or on all the things we cannot do.

Shift your focus to the positive. Think about all the things you are and all the things you can do!

Don’t ever forget, YOU were fearfully and wonderfully made.

Go out today and spread your wonderful-ness around to all those you encounter.

πŸ’šπŸ’šπŸ’šMuscular Dystrophy Awareness MonthSometimes the greatest gift you can give someone is to simply include them.While at...
09/11/2025

πŸ’šπŸ’šπŸ’š
Muscular Dystrophy Awareness Month

Sometimes the greatest gift you can give someone is to simply include them.

While at first glance that might look like a simple statement but to someone with a disability who has been left out, not invited, and turned away, that statement is precious.

People with disabilities are just people and they long to be included in all aspects of life.

If you have a friend with a disability don’t assume what they can and cannot do! Ask them. I promise they will appreciate you taking the time to ask.

Even though I have been left out over the years because of my disability there were countless times my friends and family would think outside the box to make things work.

I have been piggy backed in houses and then pushed around in an office chair.

I have been carried on boats to enjoy the summertime fun.

I have driven my wheelchair up four wheeler ramps because that’s what worked at the time.

I was whisked up a flight of stairs in New York City by a complete stranger to make sure I didn’t miss my dinner reservations.

I have been carried to the beach just so I could put my feet in the sand, hear the ocean, and feel the sun on my face.

There are so many wonderful memories I have because I was included.

Today, I encourage you to simply include someone with a disability.

πŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šSeptember is Muscular Dystrophy MonthThe side effects of LGMD2B are vast and never ending.I became an advo...
09/10/2025

πŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’š
September is Muscular Dystrophy Month

The side effects of LGMD2B are vast and never ending.

I became an advocate as a teenager without even realizing it. During the few years I was misdiagnosed with Polymyositis, there were several different drug therapies that I tried without success (of course because I was misdiagnosed).

At one point I was on 100 mg of prednisone a day. Prednisone at such high doses has many terrible side effects and I think I experienced them all. After gaining 60+ lbs and needing a wheelchair because of steroid induced myopathy, I told my doctor I was coming off the prednisone. We could do it my way (quitting cold turkey) or his way (a gradual tapering) off the medication. Thankfully I had a wonderful doctor and he agreed that the prednisone was doing more harm than good.

That was one of the first times I can remember advocating for myself and what I felt was best for me. Over the years there have been countless times I needed to advocate for myself. No one knows me or how LGMD2B affects me better than ME.

Today I encourage YOU to use your voice.

Finding and using my voice has been life changing! I promise it will be the same for you!

Started the morning at Tennessee Tuesday and had the pleasure of meeting Sen. Marsha Blackburn and Senator Bill HagertyI...
09/09/2025

Started the morning at Tennessee Tuesday and had the pleasure of meeting Sen. Marsha Blackburn and Senator Bill Hagerty

I'd say we are off to a great start here in DC!

09/09/2025

21K Followers, 110 Following, 1,573 Posts

Say a prayer and send good thoughts our way please. Tomorrow the LGMD community will flood the halls of the Capitol in D...
09/09/2025

Say a prayer and send good thoughts our way please.

Tomorrow the LGMD community will flood the halls of the Capitol in DC!

I’m excited to share this experience with my girl. We have meetings scheduled with our Congress leaders all day long!

Thank you to The Speak Foundation for providing this advocacy opportunity!

Throw it around like confetti!!
09/08/2025

Throw it around like confetti!!

09/08/2025

All ADA hotel rooms are not the same!!

It’s a good thing lime green goes so well with PINK. 😜 πŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šSeptember is Muscular Dystrophy Awareness Month Lim...
09/07/2025

It’s a good thing lime green goes so well with PINK. 😜

πŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’šπŸ’š
September is Muscular Dystrophy Awareness Month

Lime green is the ribbon color that represents LGMDs.

09/06/2025

It’s bath time!

09/05/2025

Day 4 LGMD Awareness

Address

Chattanooga, TN
37421

Alerts

Be the first to know and let us send you an email when Inclusion is Bliss posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Business

Send a message to Inclusion is Bliss:

Share