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 How to Let Them Go SPMS and My Body Image…
Is Multiple Sclerosis its own worst enemy?
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
Hàbits saludables per viure millor amb EM
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: Alimentació equilibrada Una dieta rica en fruites, verdures, cereals integrals…
Principals tractaments farmacològics per a l’esclerosi múltiple
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 vida de les persones afectades. Enfocament del tractament L’abordatge…
An Attitude of Gratitude: Finding Light Even in the Darkest Moments
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 have, we act as if it’s already here—allowing the universe…
Fallosophy Is Here! My Book About MS.
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 about living with MS. It’s about falling down and getting…
Of Clocks, Kids and Travel
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 it is, the cold, hard truth. This baby is my…
Life with MS: don’t let people steal your identity
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, the feeling of guilt is an experience that many people…
Intubated with pneumonia… Another MS tentacle
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 than a drop in my eyesight, my MS was stable…
Advocacy, MS and Chronic Illness
Time for a quick catch-up with what’s been happening in my MS-y life (MeSsy?). To be honest, I can’t quite … The post Advocacy, MS and Chronic Illness appeared first on . 6 Tips to Keep Working at Your Health Goals – Despite Living with Chronic Illness Living with a Progressive Chronic illness…. Source: trippingthroughtreacle.com