Christ follower, lucky wife of @bga090199, #NBCT teacher, rare disease warrior- #spinocerebellarataxia2, Go Hogs 🐗, #BLM 🖤, Just Love!!

Joined February 2015
75 Photos and videos
I’m 1 proud aunt! Andrew, you showed the world your heart today. Mom surprises teen son with a power wheelchair. His reaction will bring you to tears today.com/parents/family/mom… via @TODAYshow @DuchenneXchange @DuchenneNow @CoalitionDMD @RareDiseases
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I’m curious. I have Spinocerebellar Ataxia Type 2 and my nephew has Duchenne Muscular Dystrophy. How common is is for 1 family to have 2 separate rare diseases? @RareDiseases @NAF_Ataxia @DuchenneXchange @TheMightySite @hopeforataxia
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Oh, and my granddaughter has CP!
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1st ride of the summer. I’m so out of shape but I’ll get it back! I have to find a way to continue riding during the school year.
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I’ll never forget this night. Miss Arkansas Hall of Fame induction. I share, not to receive praise, but to motivate people with disabilities to never stop.
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I had fun in Vegas last night. But what you don’t see is the 2 hour nap I had to take after walking the strip during the day just to make sure I could last at night. This is #spinocerebellarataxia Do what you can, when you can! @NAF_Ataxia
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Did you know not all handicapped tags are equal? You are only allowed to park in Van Accessible spots IF you have this decal on your license plate or hanging placard! Please don’t take up these parking spots from people who really need them. #ada @RareDiseases @NAF_Ataxia
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Christie Alexander retweeted
Looking for a 9-12 English teacher in Sheridan, Arkansas if you know anyone.
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Me after my inaugural bike ride this morning. I think my dad (who has had his @Catrike for 10 years) tried to kill me. I can’t wait to do it again! #dontlimitme @RareDiseases @NAF_Ataxia @AtaxiaCentreUCL
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I finally got my new @Catrike (the Trail model)!!! I haven’t been able to ride a bike in years! Freedom! @NAF_Ataxia @hopeforataxia
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Good morning to the 2-3 people who actually read my posts. 😄 I hope you have a great day! Remember, love all!!
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Fan girl much? When I meet Rachel Lindsey from @BacheloretteABC - YES! #gyto2022 @kaitlynbristowe
I try to live my best life even though I have a rare disease. Sometimes it’s hard but easier when you have friends to help when you get tired! Ok #gyto2022 let’s go! @burgessdave I’ll see you tomorrow! @NAF_Ataxia @TheMightySite @RareDiseases @RickJetter
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Arkansas, you made HERstory this weekend! Just look at your new Miss Arkansas and Miss Arkansas Outstanding Teen!! How many little girls will look up at the both of you and have their lives changed? 🖤❤️🖤 @MissAmerica @ebonymitchell00
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I love @Starbucks They are a great company. That is all.
This is a video I made to show what it’s like living with a rare disease. It’s called-So I’m actually not living with OPCA. I have Spinocerebellar Ataxia Type... youtu.be/6ZL5VD4YP4c via @YouTube @NAF_Ataxia @TheMightySite

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I forgot to tag @pcssdschools 😳 Sorry!! You need to know of the great things happening in your schools. 😉 #pcssdproud
Our class was recorded today by the department of education to help other teachers. It also goes to show that people with disabilities can do anything they put their mind to! @bethhill2829 @mr_hayes @NAF_Ataxia @RickJetter
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Our class was recorded today by the department of education to help other teachers. It also goes to show that people with disabilities can do anything they put their mind to! @bethhill2829 @mr_hayes @NAF_Ataxia @RickJetter
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My class was learning “Q.” I said that I was a queen and had a crown but kept forgetting it. 1 girl wouldn’t give up😄so my mom brought it. I let them try it on and said hi to King or Queen.. Thanks @MissAmerica for letting me make a diff. with children 23 years later! ❤️👑
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I wish you could have seen their sweet faces. They were in awe. I hope it was a memorable day for them.
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