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…6 min read·Sep 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…6 min read·Sep 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…5 min read·Jun 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…4 min read·Dec 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…3 min read·Nov 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…5 min read·Jul 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…5 min read·Jul 5, 2015--2--2
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…4 min read·May 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:3 min read·Mar 29, 2015----
