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The Mitochondrial/Motility Journey
#MitochondrialAwarenessMonth Sept 22 our online/ offline awareness day! How do I tell you about my mito? The easiest way is to describe how your organ systems behave when you age. Yet in a mito malabsorption dx my bones were 86 yrs old but I was approximately 40 (when this began.) my hearing & eyesight declined. I had cataract implants way earlier than you would anticipate. My GI issues … at…
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Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
Second Place - What It Could Mean
Second Place – What It Could Mean
Stand tall
All is not lost
There will be a record keeping
All is kept in its place
A close second is not an embarrassment to our tomorrow
It is a marker for Justice
She will come
Ever so slow, it may seem
Like Josephus
back in his day
accounting His days
There is always a close second
Like in “The Social Network”
The movie about Facebook
All may seem like it’s wonderful, in dollars and cents, but…
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Our World Today
I feel at a loss, not as a chronic warrior of incurable illnesses, nor with my advocacy over adversity from day to day in prayer to keep my mind and thoughts in a peaceful strength of optimism and positivity. No, while challenging, I feel secure within my warrior journey. I may lack energy or health, but I am optimistic and positive about my day, hour, minute, moment. I am at a loss to understand…
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Thank you to all who posted & acted in #advocacy yesterday’s #Green4GP to #CureGP I truly appreciate each and every act of advocacy! We created change with every single post! I believe every time we post a video, a photo, poster, meme, etc we turn up the volume on our advocacy! Thank y’all so very much! Now we continue our advocacy journey! On Day 26 of our #Gastroparesis advocacy month! As our #warriors know our journey is 365/24/7 so we are here every #SpoonieSunday when our spoons allow! Does any one else like the movie #DangerousMinds? The teacher played by Michelle Pfieffer @gorgeouspfeiffer tells the students they all have A’s and it is up to them to them whether they lose their A’s. I love this approach as an optimistic positive perspective!!! It is us! We have already succeeded in our campaigns and events because one or more voice or action speaking that would have not otherwise been speaking is absolutely a success! We, you, all of us are a success in every advocacy step we make! So I hope this provides you with a bit of encouragement, motivation, on this day going forward may your day be blessed with comfort and strength 🧤🙏🏼🧤💚💙🙏🏼🙏🏼🙏🏼💚💙🚣🏼♂️🚣🏼♂️🚣🏼♂️ @gimotility @digestivehealthmatters @aprilgqg @bundytr5 @melissaadamsvanhouten @mcbanecarolyn @nkotbangelwingz @steventrotter @walton_raven @dr.mamina @cherylraudebaugh @chronically.christina @docevans1972 @christinemiserandino @umdf @mitoaction @us_pain_foundation @medivizorteam @wegohealth @hesaonlineorg @monitakespics @itskimmyjo @mo_2013_ @crystalephillips @daisymariebonilla @laurenglowss @fredasteve1 @gastroparesisgoofball @legalizeitlala @kark4news @wmcactionnews5 @angel_dunlop @csaltrelli @y._e._s._s._i._e @gpwarrior
#Green4GP to #CureGP #Gastroparesis #Advocacy over #Adversity We each have a unique voice to be heard, expressed, shown, as #Advocates #Warriors #GPReporters #OnlyYou can add your #Special #Greenness While we share #Motility diagnoses #CIP #SIBO #ColonicInertia #Crohns #Barretts & many more.We express our variations in our own unique way! Seeing & showing these variations helps others who think they are alone because their symptoms do seem to fit the “pattern.” When there isn’t a fixed pattern nor is there a fixed treatment (at this time there are no successful treatments for Motility diagnoses like Gastroparesis) protocol because what works for one may not work for another patient. The longer we seem to walk in our chronic journey the higher our drug sensitivity seems to be. What I once was not allergic to I am suddenly having a reaction to it isn’t because we are weak, but because our body’s resistance is changing the longer we live in a chronic body with malnutrition and dehydration. Our body’s ability to fight infection or resist viral, viruses seem to evolve.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
August 25th #Green4GP to #CureGP 2nd Annual #TheEvent
August 25th #Green4GP to #CureGP 2nd Annual #TheEvent
We are each #TheEvent in advocacy over adversity 365/24/7 living lives with chronic illnesses. You are warriors on every level of your lives in various ways in multiple chronic communities, many of us overcome multiple diagnoses on a daily basis. Choosing to focus on our truth before our diagnosis while accepting our growth in how the diagnosis/es have stretched us in numerous ways. Over the…
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#Green4GP to #CureGP #Green4Mito to #CureMito #Cures #Advocacy confronting #Adversity impacts us all! Creating change #StrongerTogether #Gastroparesis #Motility #Incurable2Curable #Invisible2Visible via @RiplApp please note, the diagnosis and treatment manual was a textbook used in 1969 to teach physicians on the pathway to be a physician in 1969. It was my Dad’s .. I noticed it years ago while looking for something else. I had originally kept the book because it was one of my Dad’s books. He passed away when I was 15 and it had a connection to what we what we now know was a Motility/Digestive Disease issue. I look at the world from a perspective of no coincidences. It is not surprising our community is provided insight into the source of how this problem was addressed. Why is it still riding a wave of resurgence in Motility community? Perhaps it is the frustration of lack of answers? Perhaps it is an inherent gender bias in our culture? Whatever it is I believe our compassionate, empathetic, advocate Voices will be our solution to this issue. If we are calmly, consistently dedicated to standing up together for each other.. we will baby step our way forward. It will not be fast enough. I will not lie. Yet we will get there! Yesterday wasn’t fast enough, but inaction without applying our vast amount of unique talents, skills, spoons, passion, would be an unanswerable question of endless speculation. Why ask it when we know what our possibilities are when we all speak up & out? It is like hearing a Hallelujah Choir! When advocates from many Chronic Communities join in as one it is an amazing sight! #WeSeeYou #WeHearYou #WeFeelYou #WeAreYou @gimotility @tippedmug @cecielro @aprilgqg @mcbanecarolyn @bundytr5 @gpwarrior @melissaadamsvanhouten @umdf @mitoaction @us_pain_foundation @walton_raven @cnn @dazzle4rare @monitakespics @spinalcsfleak @laurenglowss @steventrotter @andersoncooper @aliciakeys @tonyscruggs
#TheEvent #Green4GP to #CureGP #Green4Mito to #CureMito
#TheEvent #Green4GP to #CureGP #Green4Mito to #CureMito
#TheEvent #Green4GP to #CureGP
#Green4Mito to #CureMito
It is my pleasure to announce the dates for the second annual #TheEvent #Green4GP to #CureGP on August 25, 2018
With -> September!
#Green4Mito to #CureMito Sept 22, 2018 as an Awareness Campaign online & offline!
Please be as loud & lively as your spoons allow!
No stressing just blessings for awareness, encouragement, empowerment,…
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