Sweet Nectar Society

 

PHOTOGRAPHY WITH A PURPOSE

Sabrina Ellis :: Multiple Myeloma

Sabrina Reneé Ellis, a 47-year-old mother to four and grandmother to five, was nominated for a photography session from Sweet Nectar Society through the women’s support group HOW (Helping One Woman at a time).  Sabrina received a diagnosis of multiple myeloma, a type of bone marrow cancer, on July 7th of 2011.

Sabrina is a longtime resident of Tulare County; she was born in Pixley and moved to Tulare at age 22.  She has worked as a corrections officer for the State of California for 21 years.  Sabrina enjoys attending church and spending time with her family, including her two sons, Travis (24) and Dyllon (19), and her two daughters, Daviél (26) and Antonia (16).

After receiving her initial diagnosis of multiple myeloma, Sabrina underwent three months of chemotherapy and radiation treatments before receiving a stem cell transplant in late October of 2011.  Her cancer was in remission for two months, until January 17th of 2012, when it was confirmed that the multiple myeloma had returned and was more aggressive than noted in her initial diagnosis.  She continues to receive chemotherapy as a comfort measure.

Sabrina expresses deep love and thankfulness for her kids and everything they have done for her.  She appreciates that all of her children, including her adult children who do not live or work in town, dropped everything they were doing to come home and “take care of mamma,” and she values every day she gets to spend with them.  Sweet Nectar Society is honored to be able to give the gift of photography to this amazing family to commemorate Sabrina’s beautiful life, filled with courage and love.

 

Michael+Mac=Brothers :: Duchenne Muscular Dystrophy

Mac was diagnosed with Duchenne Muscular Dystrophy on January 6, 2012.  Up to the point of his diagnosis with DMD Mac went through numerous blood draws- but he was a brave little boy and never cried during the process. His extremely elevated CK (liver) enzymes made it clear to the doctors that something was going on with his muscles. A liver biopsy was done, followed by DNA testing, It was at this time Mac was diagnosed with Duchenne Muscular Dystrophy.

DMD is a non-curable and fatal, genetic disease. Mac’s loved ones hold onto the hope that a cure will become available in the near future, but in the meantime, their ultimate priority is to get Mac the best care available, in order to give him the best quality of life possible.

Dr. Brenda Wong has dedicated her life to researching and developing treatment for Duchenne Muscular Dystrophy patients. Mac’s family hopes to meet with Dr. Wong in Cincinnati, Ohio this summer to learn more of his disease. Before this can be made possible they will need to raise $4,500 to cover costs.

Please consider opening your hearts to help make a life changing difference for Mac. Donations can be made to Sweet Nectar Society for Mac.

Photography by Brittany Wilbur
Clothing by Espi's Kids
Music: Third Day, Love Song

Alena :: Acute Undifferentiated Leukemia

Alena was Diagnosed with ACUTE UNDIFFERENTIATED LEUKEMIA in 2011.

Alena celebrated her second birthday on March 5, 2012 with gifts, a homemade cake, her mom, and the nurses at Valley Children’s Hospital.  This sweet little girl from Merced, California is currently undergoing chemotherapy and awaiting a bone marrow transplant to treat her acute undifferentiated leukemia.  Alena was diagnosed in May of 2011, and after undergoing chemotherapy, was placed in remission in October of last year;  two months later, the leukemia was back.  Now she lives at Valley Children’s with her mother, as she finishes her chemo and awaits the results of a bone marrow biopsy, and ultimately for her name to reach the top of the transplant list.

Alena is such a fun, spirited, playful toddler! She loves to play on the swing set, read Silly Sally, and clean with her toy vacuum.  Barney and Elmo are her favorite characters, and she loves to eat rice and noodles.  Alena’s mom and dad hope to take Alena, along with her two older brothers and one older sister, to visit Disneyland once Alena is in remission again and back home.  They also hope to have a new home to live in once the transplant has taken place, complete with Alena’s very own swing set in the backyard.  What a precious, beautiful, courageous little girl.

Photography by Brittany Wilbur

Bio by Alex Smith

Clothing provided by Espies Kids

Jaden :: Rhabdomysarcoma

Jaden was diagnosed with Rhabdomysarcoma on March 12, 2011.

On March 9, 2011, five year old Jaden was admitted to Children’s Hospital for what was believed to be compacted bowels.  There they found a tumor the size of a small cantaloupe in her stomach/pelvic area. On March 12th, her family received the news that it was cancer.  In just a matter of days, Jaden began the first of 54 weeks of chemotherapy and 5 weeks of radiation. To the doctors amazement, during her 5 weeks of radiation treatment, Jaden managed to lie perfectly still without being sedated.

After completion of radiation, the tumor had shrunk down to the size of a ping pong ball and was successfully removed on September 6th, 2011. Miraculously, the tumor was not attached to anything in her abdomen. Jaden is currently in week 39 of her treatment and will finish up in May.  She doesn’t mind her chemo treatments and lack of hair, because she knows it’s helping her get better. She’s just happy to not have that pain in her tummy anymore!

After treatment she looks forward to getting back to the things she loves, like ballet class, soccer, and Bible class. But right now, she’s content to help mom around the house with her brand new baby sister, paint everyone’s nails, dance along to her favorite Wii game, play with Barbies, and play dress up. Jaden truly is an inspiration.

Photography by Brittany Wilbur

Bio by Kimberly Dodson

Clothing provided by Ga Ga Chic

Abigail :: Acute Lymphoblastic Leukemia

Abigail was diagnosed with Acute Lymphoblastic Leukemia in the summer of 2011.

“It all started with what they thought was a swollen lymph node, then turned to 104 degree fever for 8 days with a diagnosis of Salmonella in her blood. Her blood levels never returned back to normal after treating her initial diagnosis, which concerned the doctors. They eventually found out through bone marrow biopsies, bone scans, CT scans, lots of poke-y things, etc. that her small little body had rapidly growing blast cells, leading them to the sad and scary diagnosis of ALL.

Abigail started chemo the day after her diagnosis… a combination of 3 different chemos placed in her spinal tap. She is on a rigorous treatment for the first 6 weeks, with chemotherapy treatment lasting for the next two years.” Abigail’s Auntie, Katrina Bartel shares on Abigail’s Bling for Balding Beauties fan page.

I feel so blessed to have had the opportunity to photograph Abigail for the second time this morning. She is absolutely adorable and all girl. She loves her nail polish, lip gloss, and most of all BUBBLES. I look forward to more shoots with this sweet girl!

Photography by Brittany Wilbur

Clothing provided by Espies Kids

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Session Info

SWEETIE SESSION

•A free photography session

•A digital gallery of images

•A keepsake book

•A platform to raise awareness

•Story shared for support

PATIENT SPOTLIGHT SESSION

Provides documentary type photography session to patients currently admitted to the hospital.

•A digital gallery of images

•A keepsake photo

FOCUS SESSION

Portrait session events designed to raise awareness to a specific diagnosis, build community, and celebrate Sweeties.

•A digital gallery of images

•A keepsake photo

(559)408.5969 | info@sweetnectarsociety.org

Sweetly rooted in California