HunterKeldans Sacral Agenesis Fund

My 3 Year Old Son HunterKeldan Has Been Dianosed With A Rare Genectic Disorder Called Sacral  Agenesis. ( Caudal Regression).  It Is Difficult For Him To Walk And Move Around As He Has Pain In His Leg's And Back. He Also Has Bowel Issues Due To Anorectal Abnormalities From This Disease.  This Is A Degenerative Disease Of The Spine. Which Affects His Movement, Nerve Ending's, Neurological Development, And Physical Development. He Has A  Long Road Ahead Of Him With Many Upcoming Treatment's With Specialist's, Urologist's, Neuorologist's, Physical Therapist's, Surgeon's, Etc.... Just To Name A Few. My Day's And Night's Are Long  And  Extremely... Busy. HunterKeldan  Goes Thru Approximitely 3-5 Pamper's Per Hour At Time's Due To His Bowel Deformity. And I Have To Spend A Good Portion Of My Day Having To Carry Him Around Because He Is Unable To Walk, His Leg's Hurt And He Is Tired. And Then I Have To Do The Same With His Baby Sister MiaBella Whom Is Not Walking Yet Do To The Possibility That She May Be Suffering From The Same Genectic Disorder. Testing For Her Is Underway. HunterKeldan Is Also Small From His Disorder. He Is 3 Year's Old And Can Fit Into Size 6 Month's Old Clothe' s In Waist And Width In Pants. His Length Is 18 Month's. We Already Have Medical Bill's In Excess Of 47,000. My 17 Month Old Daughter Is Also In The Process Of Possibly Being Diagnosed With The Same Genectic Disorder. Which We Pray That She Does Not. We Are Asking For Any Amount Of Donations To Help With Any Costs Of Medical, And Medical Related Expenses. And For Needs To Help HunterKeldan Be More  Comfortable On A Daily Basis. So Please..... Prayers Are Needed Along With Whatever Donation's That You Can Make. Every Dollar Help's. This Is Going To Be A Long Journey All Around For Me And My Children. We Thank All Of You For Taking Your Time To Read This And For Your Support. 
Michaela Nolan And Family