Matthew Harty Camper Fund Scholarship Application 2025 Matthew Harty Camper Fund Scholarship Application Sponsored by MitoAction "*" indicates required fields Name of Applicant* First Name Last Name Applicant Address* Address Line 1 Address Line 2 City AlabamaAlaskaAmerican SamoaArizonaArkansasCaliforniaColoradoConnecticutDelawareDistrict of ColumbiaFloridaGeorgiaGuamHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaNorthern Mariana IslandsOhioOklahomaOregonPennsylvaniaPuerto RicoRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahU.S. Virgin IslandsVermontVirginiaWashingtonWest VirginiaWisconsinWyomingArmed Forces AmericasArmed Forces EuropeArmed Forces Pacific State Zip Code EthnicityCaucasianAfrican AmericanLatino or HispanicAsianSoutheast AsianNative AmericanNative Hawaiian or Pacific IslanderTwo or MoreOther/UnknownPrefer not to statePrimary LanguageArabicEnglishSpanishBengaliBhojpuriChinese- MandarinChinese – Wu or ShanghaineseChinese – Yue or CantoneseFrenchGermanGujaratiHausaHindiIgboItalianJapaneseKoreanMarathiPersian IranianPortuguesePunjabiRussianTagalogTamilTeluguTurkishUkrainianUrduVietnameseOtherPronounhe/him/hisshe/her/hersthey/them/theirve/ver/visxe/xem/xyrze/zieApplicant Phone*Applicant Email* Applicant Birth Date*Please use the following format: XX/XX/XXXXApplicant Gender*MaleFemaleGender DiverseWhat is your mito diagnosis?* Alpers’ Disease ACAD9 Deficiency Autosomal Dominante Optic Atrophy (ADOA) Barth SyndromeA rare, genetic disorder of lipid metabolism that primarily affects males. CACT Deficiency CPEO Complex I Deficiency Complex II Deficiency Complex III Deficiency Complex IV Deficiency Complex V Deficiency CoQ10 Deficiency CPT I Deficiency CPT II Deficiency Creatine Deficiency Syndrome CUD/Primary Carnitine Deficiency Friedreich’s AtaxiaFriedreichs Ataxia GAII/MADD Deficiency Kearns-Sayre Syndrome (KSS) Lactic Acidosis LCHAD Deficiency Leigh Syndrome Leukodystrophy LHON LHON Plus Luft Disease MCAD Deficiency MCKAT Deficiency MELAS MEPAN MERRF MIRAS MitochondrialRelated to the mitochondria. Cytophy Mitochondrial DNA Depletion Mitochondrial Encencephalopathy Mitochondrial Myopathy MNGIE M/SCHAD Deficiency MMDS NARP Pearson SyndromeA rare disease that targets the bone marrow and pancreas. Through dysfunction of cells in the bone marrow that produce white and red bloods cells along with platelets. POLG Mutationsgenetic variant, genetic change POLG 2 Primary Mitochondrial Myopathy Pyruvate Carboxylase Deficiency Pyruvate Dehydrogenase Deficiency PDCD SCAD Deficiency Thymidine Kinase 2 Deficiency (TK2) VLCAD Deficiency Undiagnosed Other High School Name*High School Location* City AlabamaAlaskaAmerican SamoaArizonaArkansasCaliforniaColoradoConnecticutDelawareDistrict of ColumbiaFloridaGeorgiaGuamHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaNorthern Mariana IslandsOhioOklahomaOregonPennsylvaniaPuerto RicoRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahU.S. Virgin IslandsVermontVirginiaWashingtonWest VirginiaWisconsinWyomingArmed Forces AmericasArmed Forces EuropeArmed Forces Pacific State SAT or ACT Score*GPA*Please use your most recent GPACollege Name*College Location* City AlabamaAlaskaAmerican SamoaArizonaArkansasCaliforniaColoradoConnecticutDelawareDistrict of ColumbiaFloridaGeorgiaGuamHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaNorthern Mariana IslandsOhioOklahomaOregonPennsylvaniaPuerto RicoRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahU.S. Virgin IslandsVermontVirginiaWashingtonWest VirginiaWisconsinWyomingArmed Forces AmericasArmed Forces EuropeArmed Forces Pacific State Degree & Major to be pursued*Have you previously been awarded the Matthew Harty Scholarship?* Yes No If yes, please list which school year(s) you received the scholarship.*Transcript/Enrollment VerificationIf you have already enrolled for the fall semester, please attach proof of enrollment. This is not required to receive the scholarship, but must be sent before award is issued.Max. file size: 2 GB.Physician LetterIf you have a physician letter already, you may upload it here, otherwise, your physician should email it to scholarship@mitoaction.org or fax to (888) 648-6228.Max. file size: 50 MB.Extracurricular Activities*(sports, music, art, work, hobbies, etc.). You may include this as an attachment if necessary.Extracurricular ActivitiesPlease upload here if needed.Max. file size: 2 GB.Volunteer & Community Service Activities*(especially those that impact children and teens with chronic medical conditions or special needs). You may include this as an attachment if necessary.Volunteer & Community Service ActivitiesPlease upload here if needed.Max. file size: 50 MB.Please include a typed, single-space, one-page essay that addresses the following question:*How will the Matthew Harty scholarship help you to succeed in college and how has mitochondrial disease affected your life and your education in a way that can help you to be a source of inspiration to others struggling with the disease?Max. file size: 2 GB.Please attach a photo of yourself.*Photo will only be used if you are a recipient.Max. file size: 2 GB.CAPTCHANameThis field is for validation purposes and should be left unchanged.