El proper dissabte 19 d’abril, la música i la solidaritat es donaran la mà en un esdeveniment especial per donar suport a la recerca i la lluita contra l’Esclerosi Múltiple. Es tracta d’un concert solidari de gòspel que comptarà amb la participació del Cor Gospel…
Hi all, I hope that you are all doing well? Yet again, I can’t believe where the time goes – … The post New Meds, New House, New Feelings about My MS… appeared first on . Living with a Progressive Chronic illness…. Expectations – Learning…
MS doesn’t concern itself with how long your bucket list is. It adds unexpected chapters to your story where you didn’t want any, and it’s up to us to fill these pages advocating for our own new normals, even when we feel ill-equipped. Source: irelandms.com
L’esclerosi múltiple (EM) és una malaltia crònica que pot afectar la qualitat de vida. Tanmateix, uns hàbits saludables poden millorar el benestar i afavorir un estil de vida actiu. A continuació, presentem alguns consells que, aplicats diàriament, us poden ajudar a gestionar millor la malaltia:…
Tot i que encara no existeix una cura definitiva per a l’esclerosi múltiple, hi ha diverses opcions terapèutiques que poden ajudar a controlar els símptomes, reduir la progressió de la malaltia i disminuir la freqüència dels brots. Tot plegat contribueix a millorar la qualitat de…
It was May 2024 when I wrote this title. Even then, I knew that gratitude is one of the most powerful emotions for manifesting anything. When we express gratitude, we energetically align with what we wish to attract. Instead of yearning for what we don’t…
It’s official…Fallosophy, my book about MS is finally here! And I’m so glad it got published before I could trip on something new and have to add another chapter. Fallosophy: the elevator pitch (because, let’s face it, I don’t do stairs) Fallosophy is a memoir…
Less MS, more old I am old enough to be this little guy’s grandmother. It might be a leap, but in actuality, I am old enough to be his great grandmother too. When the hell did that happen???? It just doesn’t seem real but there…
The feeling of stigmatization is a real one, especially when you have invisible disabilities when you don’t sit in a wheelchair (yet). It is also why society at large feels it has the right to question your medical status, whether asked for or not. Therefore,…
It’s taken me a while and many attempts to write this post, I’m still carrying trauma from the experience. I know I’ve been very quiet since the birth of my daughter, which was hard in ways I didn’t expect – mentally and physically. However, other…