MS'ed With the Wrong Girl
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- Опубліковано 10 вер 2024
- Exhausted but never tired, a feisty woman living with MS pushes from one activity to another wondering daily if life can ever be normal.
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Great video Patrycia. You are such a great spokesperson and a unbelievable fundraiser for MS! I've been visiting the MS clinic in Edmonton as well since my diagnosis in 2013. I'm so thankful for the MS clinic and the advances in research we've helped fundraise for by riding MS Bike Leduc to Camrose (I've been riding it as well since 2015). I'm thankful for the advances and choices in disease modifying drugs (dmd) that we have available to us now. Fortunately I had 10 years with very few MS symptoms on my 2nd dmd. I'll be switching to my 3rd MS dmd at the end of this month and hoping that will put an end to this current disease progression/activity and give me another 10 years without further advances.
Thank you for doing this inspiring documentary! I was diagnosed a year and a half ago and it's terrifying to think of what can happen in the future, that is why I try very hard to not think about it often and keep living my life the best way I know how to...One day at a time! Thx again and God bless!
Since my diagnosis in 2011 I too share in a similar rollercoaster of life with MS. Thanks for sharing your story. I chose to start copaxone, a disease modifying therapy, once I was having yearly relapses which kept taking my vision. Luckily I've been relapse free for near 4 year now though do face some lingering visual disability. I think there is def a use case for their [medications] inclusion as treatment, just as their is for exercise. No shame or wrong choices in taking medication or prescription s (which now includes exercise) that have been tested and proven to be effective in reducing the damage MS trys to pull on us. Keep fighting!
i was diag. at age 35,now 70. my motto YESTERDAY IS HISTORY, TOMORROW A MYSTERY, TODAY A GIFT,THAT IS WHY WE CALL IT THE PRESENT.. NEVER wasted time on WHY ME just take the M.S.PUNCHES a day at a time.
Hi I was diagnosed at age 25 I am now 56 and you sound like you have had a MS for about the same amount of time. How are you doing now. You have a great attitude contact me anytime at 780-512-5108 thanks
You are such an inspiration to so many and your optimism speaks volumes. You will beat this !!! Many people suffer with MS and should be as positive as you. together we will find a cure !! And thank you Kelly for doing this story....just another amazing video!!!! Congratulations
Patrycia - you are an inspiration. Your story has helped me through the pain of my father's death from MS and has encouraged me through years of Bike Tours in the rain and wind, just knowing the strength of your commitment and love. Thank you for this...
Thank you for sharing this
Thank you for your story. Patrycia is one gutsy and feisty lady. I'm so happy to know her.
Thank you! My symptoms just started around June 23rd and have progressed rapidly. My onset is a bit older in my mid-40's but this can happen to anyone.... Still waiting for antibody test results from Calgary but I will learn & fight this! Great documentary!!
Thank you for sharing your story! 💛
Well done story - thanks for sharing your story Patrycia ;)
i’m curious as to why she doesn’t want to get any treatments such as infusions or pills to decrease lesions and relapses. exercise is wonderful too but could be used in tandem with other disease modifying therapies.
Excellent!
Keep up the fight!!!