Loving Our Parkinson's Body

Loving Our Parkinson"s Body...even for healthy people loving ourselves can be hard. How do we love our Parkinson's Body if it makes us feel embarrassed or ashamed, or doesn't do what we want it to do. This is a short meditation on loving ourselves Parkinson's and all!

[@alittlebitshaky]

Being confident and comfortable with yourself can be a battle. And adding PD to the mix is challenging.

[@MikeMercury]

accepting the way we are is real important

[@Longshanks1956]

Sending you much love.❤

[@andyfletcher3150]

For some people social nudity is a great way to learn about body acceptance and loving the skin you're in. Through nudism you learn that without our clothes we are all the same no matter what shape. This is expecially true for those with Parkinson's. Accept your body as it is.

[@leonardgebhart2064]

Thanks so much for this 🤗🥰

[@davidhughes5998]

You are inspiring and brave, thanks again.

[@MikeMercury]

so brave lady .....merci for sharing

[@clicgear100]

You are so brave, and such a good outlook. God bless you.

[@ericzeidman9845]

God Bless you, you are wonderful

[@SDWP]

I love this! We have to treat ourselves like we'd treat others....with respect and love. You're absolutely right...we all have something amazing to offer. Love the way you did this video....very cool.

[@LifewithParkinsons]

Hi Jennifer thank you for those positive thoughts and excellent reminders❤🎉😊

[@bonnieschwartz8087]

You said it perfectly... once again. A reminder we all need at some point in life, and at whatever point we are in this PD process. 💜

[@meganransmeier]

This is beautiful! Thank you for sharing so vulnerably with this community.

[@JeremyMcdonald]

What a fantastic perspective! We all need to hear this, Jennifer! Thx for being so vulnerable 😎

[@jimmcconnell7328]

Your wriggling seems so much worse. Is this due to the meds wearing off or the condition itself? I’m a senior and I feel my body is starting to let me down a little more each year that passes. My morning stiffness is worse and so is my balance issues. I’ve been trying out B1 and it does help with the fatigue. There is always the concern about depression coming into the picture. I can’t take antidepressants due to advancing kidney disease. How are you doing ? How do you keep your spirits up?

[@sharoncribbs7516]

Jennifer, you are very brave to show this side of PD. When is your dyskinesia the worst, when your meds are running out? I am going into my 3rd year. I havent had the dyskinesia but i do have restless legs. What you are going thru in this video seems to be similar but your whole body is involved. I can only imagine how uncomfortable that is. Do you feel it is a side effect of meds or progression of the disease? Thank you for sharing your life with pd with all of us. ❤ 🙏

[@robcleminson7062]

Thanks for sharing. I can identify with this Dyskinesia and experience it both when I’m wearing off and when I’m coming back on. The on sensation is so nice and I often tell my wife “here it comes” as I’m jerking all over 😀

[@MikeMercury]

youre still a lovely person

[@nickmaffei5123]

Go Girl! You are. Still attractive.

[@viproo6302]

❤‍🩹❤❤‍🩹