Queen Fatima was something like destiny for me. After I took home my first Ragdoll Queen – Candy, I kept watching her sister Cosette. She was available for a long time, so I started to think of offering home also to her. But the timing was not ideal. And finally she found her family. Later, there was Demi, who I liked so much, but when the timing was ok already, she was already reserved.

The selection of Queen Fatima

Soon, there were litter E and F at the breeder and both litters were interested for me. I knew, I didn´t want to miss them, too. There was a beautiful girl in E litter who I started watching. Then, ladies from F litter got their names – Fatima and Fanny. Those names…

Fatima was called my puppy from F litter who I kept at home and made 6 working exams with her till the age of 4 months. Freya, her sister got name Fanny in her new home. So, Fatima and Fanny were my own puppies and now – these two Ragdoll sisters were there with the same names…

As both Ragdoll ladies were beautiful, and I liked them more than the E lady, both with other variety, I finally decided to offer home to both of them. I also wanted to see, what characteristics they will pass to offspring from 3 different varieties with the same King Jami.

Character of Queen Fatima

Queen Fatima is unique. She is huge since the first moment and she loves to eat. Yes, all cats love to eat, but this one would eat anything, anytime. I use to shorten her name Fatima to “Fati”. I had to recognized that she is a bit fatty 😀 She is playful, but she is not so active, so that she stays well rounded around her belly. She is clever, communicative and really open to others. Fatima is friendly with other cats, too. She loves cuddling and is purring all the time.

Color

Queen Fatima is blue bicolor (B/B) , dilution (d/d).

Health results of Queen Fatima

Congenital hypothyroidism (CH) – N/N
Cystinuria – N/N
FXII deficiency (1321delC) – N/N
FXII deficiency (1631G>C) – N/N
Hypertrophic Cardiomyopathy (HCM3) Ragdoll – N/N
MDR1 gene variant (MDR) – N/N
Mucopolysaccharidosis type VI (MPS VI) – N/N
Mucopolysaccharidosis type VII (MPS VII) – N/N
Myotonia congenita – N/N
Polydactyly – Hw variant – N/N
Polydactyly – UK1 & UK 2 variant – N/N & N/N
Polycystic kidney disease (PKD) – N/N
Progressive Retinal Atrophy (rdAc-PRA) – N/N
Acrodermatitis enteropathica (AE) – N/N
Alpha-Mannosidosis (AMD) – N/N
Autoimmune lymphoproliferative Syndrome (ALPS) – N/N
Factor XI Deficiency – N/N
Gangliosidosis (GM1) – N/N
GM2-Gangliosidosis – N/N
Gangliosidosis (GM2) – N/N
Glycogen storage disease (GSDIV) – N/N
Head Defect – N/N
Hypertrophic cardiomyopathy (HCM1) Maine Coon – N/N
Hypertrophic cardiomyopathy (HCM4) Sphynx – N/N
Hypokalemia – N/N
Hypotrichosis/Short Life Expectancy – N/N
Congenital myasthenic syndrom (CMS) – N/N
Osteochondrodysplasie – N/N
Primary congenital glaucoma – N/N
Progressive Retinal Atrophy (PRA-b) – N/N
Progressive Retinal Atrophy (pd-PRA) – N/N
Pyruvatkinase Deficiency – N/N
Feline Spinal Muscular Atrophy (SMA) – N/N