Priscilla Cunza-MarinMS in the Time of CoronaIt has now been 7 years since my partner Chris and I were diagnosed with Multiple Sclerosis (him more than me). It has also been about a…Sep 21, 2020Sep 21, 2020
Priscilla Cunza-MarinWe Have MS: Self Care for the CaregiverEven the title of this post has me feeling a twinge of anxiety and a prickle of embarrassment crawling up my neck. My partner Chris has…Sep 29, 2018Sep 29, 2018
Priscilla Cunza-MarinThe Cruelty and Kindness of Life with MSThere is nothing good about living with Multiple Sclerosis. However many good things happen while you are living with Multiple Sclerosis…Jun 23, 2017Jun 23, 2017
Priscilla Cunza-MarinWe Have MS: Year FourJust over 3 years ago, when my partner Chris and I were diagnosed with Multiple Sclerosis (him more than me,) we were feeling all the…Dec 27, 2016Dec 27, 2016
Priscilla Cunza-MarinA Relapse and a New ApproachAt the 2 mile mark from his initial MS diagnosis, my partner Chris could sense something was off. His left arm hurt more often. He was…Nov 29, 2015Nov 29, 2015
Priscilla Cunza-MarinIn Defense of Medical Marijuana, and Ostensibly, of Our ChoicesWhile I don’t want to belabor the point, I also feel I haven’t clearly or honestly described the effects and aftermath of disclosing to our…Jul 19, 2015Jul 19, 2015
Priscilla Cunza-MarinMultiple Sclerosis, and the Dangers of ComplacencyWe’d officially had Multiple Sclerosis for almost 18 months late in 2014. Not long enough to become experts, have tons of great insight, be…Jul 5, 20152Jul 5, 20152
Priscilla Cunza-MarinGood MS Days, Bad MS Days, Terrible MS DaysMy partner Chris has RRMS (Relapsing Remitting Multiple Sclerosis.) So far his neurologist is fairly certain of this, based on his response…May 29, 2015May 29, 2015
Priscilla Cunza-MarinPlease Remember, You Have MS!The following is a list of things my partner Chris playfully tries to get out of doing by using his Multiple Sclerosis diagnosis:Mar 29, 2015Mar 29, 2015