We are still collecting submissions for the Artistry of ALS virtual gallery! Any and all types of art are welcomed and encouraged (though we are sticking to artists who are or were living with ALS at this time). Check out last year's gallery for more info: iamals.org/artistry-of-al…

Today, August 11, is my father’s birthday. If he lived he would be 81 today. I promised him before he died no matter how old I am and no matter how many titles I have, I will always remain as his little girl. I am my daddy’s little girl Today and always.

herkesebilimteknoloji.com/yazarlar/hande… Today is the day my mom passed away, But she can never die, for I have her mitochondria in me, in every cell of mine. She may pass away, but I can never let her die.

Yes please let’s reduce drug prices.

The rainbow appeared right in front of me. I hope this will be the sign of good news coming our way.

Everyday I am a scientist. Today I am also an artist at the Evanston ART Festival. ART LOVES SCIENCE FOUNDATION.

On the stage at the Democratic convention a few minutes ago, I AM ALS’s Brian Wallach and Sandra Abrevaya Wallach, whom we interviewed in June regarding their activism for ALS research

Increased drug prices is a big problem. Can you imagine that the price of an SMA treatment was $2.5 million.. Can you imagine.. Lower drug prices, make them affordable so that people do not have to choose between their drug versus bread on the table for the family.

Explore possible reasons for the elevations and what they may mean for ALS: bit.ly/4fS0iE9 #ALS #AmyotrophicLateralSclerosis #ALSDisease #ALSTreatment #ALSResearch

Is there an ALS-friendly diet, and if so, what foods are included? Get the full rundown on all things ALS and nutrition here: bit.ly/4cvI1Kc #ALS #AmyotrophicLateralSclerosis #ALSCommunity #LivingWithALS #ALSAwareness

Patients who received one year of treatment with the oral tablet experienced far better results than those who started six months later. Explore them here: bit.ly/46YoVLv #ALS #AmyotrophicLateralSclerosis #ALSDisease #ALSTreatment #ALSResearch

Therapies approved for ALS work to prevent or slow motor neuron damage. Take a look at the options here: bit.ly/474KNVK #ALS #AmyotrophicLateralSclerosis #ALSCommunity #LivingWithALS #ALSAwareness

Knowledge about the brain’s positioning system may shed light on the mechanism underpinning the devastating spatial memory loss that affects people with Alzheimer’s disease. Learn more: nobelprize.org/prizes/medicin…  #NobelPrize

Register for Cell Symposia #CSMito2024 and join us in Sitges, Spain this October for some inspiring talks, including one from Michal Minczuk Minczuk Lab on the potential of mitochondrial genome engineering hubs.li/Q02Nj5FQ0

The wonderful team at MND Australia opened up their 2024 Research symposium to all impacted by MND and End the Legacy was proud to offer some small support to allow Taryn Hunt to attend in person. Taryn is in a family impacted by genetic ALS.

feinberg.northwestern.edu/sites/alsresea… Have you registered to the 14th Les Turner ALS Symposium? Please register and retweet to inform and invite your friends.

"Liberty, the future, and freedom, everything exists with justice!" – Atatürk

Be like the flower that grows and blooms in water Be who you are no matter where you are.

Something new is cooking in the kitchen. Sleep is very important. Get your sleep, help your brain replenish.

I am happy to share with you that I am an editor at the Somatosensory and Motor Research, published by Taylor and Francis. If your research is related to somatosensory and motor systems with respect to health and disease, please keep the journal in your mind.