Amazon have dropped a new sale on select Pokemon Squishmallows, knocking over 60% off so you can grab one for as low as $6.06 ...

Pokemon plushies come in all shapes and sizes, but sometimes, regular-sized versions just don't cut it. That's where jumbo ...

The rare condition occurs when one has high blood pressure and excess protein in their urine shortly after giving birth, and can cause seizures and other life-threatening complications if left ...

An expert keeper displays a critically endangered Lord Howe Island stick insect, nicknamed "tree lobster," at the zoo in Prague, Czech Republic, Tuesday, April 8, 2025. (AP Photo/Petr David Josek ...

Zevra was granted the PRV in September 2024 by the FDA, in connection with the FDA’s approval of MIPLYFFA, the first U.S. approved treatment for the ultra-rare neurodegenerative disease ...

With the annual cost estimated to be about ₹1 crore for each child requiring treatment for ultra-rare diseases, the Medical Education Department has sought corporate support to meet the expenses.

Got back from the Tinley reptile show and wow did we bring some cool animals back to California with us... SUBSCRIBE for more ... ‘Damage Done’: New Poll Reveals Trump’s Approval Rating Here ...

After a stop-start-stop opening to Masters week, the Augusta National Golf Club is offering patrons who held tickets for Monday's practice round a double bonus that is a change in past club policy.

While she started with a Build-A-Bear, Fowler said she has about 300 Jellycats, the ultra-soft plushies taking over TikTok, while the rest are brands like Squishmallows, animal-shaped pillows with ...

AN ULTRA-rare coin has sold for a price 500 times its original face value - and the reason behind its inflated cost is bound to entice any collector. The 50p "true gem" of a coin is a "must-have ...

While she started with a Build-A-Bear, Fowler said she has about 300 Jellycats, the ultra-soft plushies taking over TikTok, while the rest are brands like Squishmallows, animal-shaped pillows with ...

According to Joe Katakowski, director of Research at the RTW Foundation, parents of children with rare diseases are the driving force behind the development of treatments for ultra-rare diseases.