Robert “Bobby” Reese #dermatomyositis #raredisease

 ** Great news from the specialist today!! Disease is controlled. Infusions down to every 4 weeks with some changes to meds. He gave the okay (based on strength tests)for Bobby to drive locally. Dr. Bhai and his nurse (who cries at everything with me♥️) both said it made their day to see us and are amazed at his progress. Big picture is another 12 months of treatments and for Bobby to stay healthy and not injure himself GOD IS GREAT !! Please continue to pray for Bobby’s improvement and for labs to stay in normal ranges. He is determined to beat this. #dermatomyositis #rarediseaseday

On 06/07/22 Bobby went to the ER with severe weakness and fatigue. After weeks of decline, in the hospital, he was finally 

diagnosed with a rare disease called Dermatomyositis. Bobby has been on a

roller coaster of painful days. Prior to being hospitalized, Bobby was a

Self- Employed hard working man. Bobby is the type of man that can fix anything and has always been there to help friends when needed. He would take calls from anyone at anytime of the day and find a way to help them. Unfortunately Bobby

cant fix this and he needs help. While we are hopeful the doctors are able to get his disease under control, he has a long road to recovery.

Any help with donations will be greatly appreciated to help this family, to help ease 

some of the burden of medical expenses and loss of income.  

 

#myositis #raredisease #dermatomyositis #autoimmunedisorders