Topic

children's rights

234 petitions

Update posted 10 hours ago

Petition to Marco mendoza, Multnomah County Courts, Marco mendoza

Finally this little guy feels safe, secure & loved.Now CPS wants to take it away from him.

My husband, Jerry and I have had little 15 month old, Ivan Fuston for almost 3 months now. We have been caring for him emotionally, financially and physically with limited contact with his mother. When we first got this little guy, he would scream for hours at a time. He did this for attention. He no longer screams, instead he laughs and plays. His vocabulary has expanded so much. His eating and sleeping habits are 100% better. He has learned to show affection properly, as well as bonded not only with us, but our children, our families. He calls them sissies and bubber... He finally feels comfortable and safe enough to relax and be a little boy. He has a schedule that he lives by, we have bought him a new full size crib, and clothes, shoes and toys. A high chair. We have not received any type of assistance or support from any agencies. We love this little boy, he's changed our lives. He calls us momma and Dada. Now cps wants to come take him because his mother is in jail and had an open case in her hometown. She didn't tell us that, only that she had charges she was going to court for. She signed a paper and wrote a letter giving us full temporary custody for one year or until she had a stable job and house of her own. She never had the paper notarized so cps says its not valid. Baby Ivan has been through enough, he's lost everything and now he finally has security, and love from all of us. Dont let them take that all away from him again.

Melissa De Voe
249 supporters
Update posted 10 hours ago

Petition to Tom Wolf, Josh Shapiro, Pennsylvania State Senate

A Safer Tomorrow for Pennsylvania Children & the Safe Child Act

http://nhprojectblog.wordpress.com/ https://www.facebook.com/groups/pennsylvaniastopabusecampaign We need the Safe Child Act and better protection of our children in Pennsylvania Family Court & Custody Crisis: Statistically, in 85% of these specific cases involving claims of abuse, it is the abusive parent who wins custody, while the protective parent, who has committed no crime against society or their child, is left powerless. In many cases there are well documented reports from trauma specialists and medical doctors, and sometimes even the court appointed psychological evaluator confirms the abuse. However, because of an outdated family court protocol dating back to the early 1970s when there wasn’t much research on the effects of domestic abuse, children are routinely put at risk.  The murder of three-year-old Kelly Williams, by her father, in April of this year in York County, PA, after it was ordered that he co parent with Kelly’s mother, is tragic, but not at all surprising to people familiar with custody court and domestic abuse. In Pennsylvania, and across the U.S. children are routinely put into the custody of dangerous parents who have harmed the child or the other parent at a rate of approximately 58,000 a year. in a recent two-year period, Dr. Diane Bartlow found news stories of 175 children murdered by abusive parents involved in child custody disputes. We have had eleven such cases in Pennsylvania since 2009.  In retrospect, it’s easy for any of us to say that Frankie Williams was dangerous; he had abused his partner, and he shouldn’t have had contact with Kelly. But legally, things that cause permanent harm to children, like domestic violence and direct abuse, are given the same weight as lesser things like a lack of health insurance, which was a factor in this case. The death or abuse of any child is tragic, but preventable abuse and deaths even more so. Kelly William’s death was preventable.  As tragic as this case is, it is not an isolated case. We have found eleven children in Pennsylvania who have been murdered during custody matters by a parent. Pennsylvania is now poised to prevent the abuse and deaths of this sector sector of children who find themselves in the family court system with strangers making decisions for them. But the larger picture of child abuse is immeasurable, and everyone can agree that greater protection is needed for the entire scope of child abuse. Protect Children Not Predators!        

Nehemiah Project
119 supporters
Update posted 3 days ago

Petition to Mr. Freddy Roosemont

Aide-nous à sauver la vie du petit Tristan

Version Française/English Version/Nederlandse Versie ---------------------------------    Aide-nous à sauver la vie de Tristan(Version Française)  Objet de la petition:  Obtenir la régularisation du petit  Tristan en Belgique car sa maladie génétique rare lui a presque coûté la vie - Tristan a besoin de soins médicaux et d’un suivi complet appropriés à sa pathologie. Cela n’est pas possible dans son pays d’origine. Synthèse de la pétition:  Tristan souffre du syndrome de Silver-Russell depuis sa naissance; ce syndrome menace son enfance et sa vie. Il est très petit pour son âge et a de multiples problèmes liés à sa maladie: hospitalisation fréquentes liées à des problèmes respiratoires sévères, hypoglycémie totale, faiblesse générale en dépit d’un optimisme contagieux, petite taille et poids, difficulté extrême à se nourrir, asthme  chronique, problème lie à l’urologie, asymétrie corporelle; mauvaise implantation dentaire,la liste est très longue… Disons simplement que ça vie n’est pas du tout facile, et bien différente des autres petits garçons de son âge. Depuis son arrivée en Belgique en 2014, Tristan a été hospitalisé à de nombreuses reprises (intervention d’urgence par ambulance à domicile hypoglycémie majeure, problème respiratoire, alimentation par IV, crises d’asthme, faiblesse générale et opération chirurgicale). En décembre 2015, à 4 ans, quand il s’apprête à aller à l’école Tristan a  fait une crise de convulsion très sévère qui aurait pu lui coûter la vie si elle s’était produite durant son sommeil (selon son endocrinologue de l’hôpital des enfants de Bruxelles (HUDERF). Malheureusement, c’est cela le quotidien du petit Tristan et de son papa. Le  dossier qu’a monté le  papa  de  Tristan,  est  appuyé  par  les  plus  grands  spécialistes mondiaux de la maladie (Dr. Harbison de l’hôpital Sinaï de New York et le Pr. Netchine de l’hôpital Trousseau à Paris, par des médecins belges de renom de l’hôpital des enfants Reine Fabiola de Bruxelles, par le docteur médecin conseil de l’ambassade belge au Rwanda) – les comptes rendus sont disponibles sur demande. Il  a  en  outre  suivi  le  processus  juridique  et  légal  en  Belgique  pour  pouvoir  suivre  les traitements en Belgique et ce de manière continue ; mais l’administration belge se mue dans un silence absolu (aucune suite n’est donnée au recours actuel). Malgré tous ces rapports de docteurs réputés et d’experts qui ont clairement soutenu que «sans traitement adapté  et amélioration de son état nutritionnel,  toute infection banale peut mettre en cause  son pronostic  vital.», l’administration  belge  (l’Office des  Etrangers: OE) et son médecin conseil ne reconnaissent pas la nécessité de séjour sur le territoire belge et  la  régularisation  de  Tristan  en  dépit  de  l’absence  prouvée  de  traitements spécialise (utilisation d’hormone de croissance), et de suivi (équipes multidisciplinaires sachant traiter la maladie) dans son pays d’origine, le Rwanda. Le Papa de Tristan est sûr que bientôt le Rwanda disposera d’infrastructure adapte a traité le syndrome rare de Tristan, mais sa vie est très fragile maintenant et il faut agir !!! Conclusion Partageons la vie avec le petit Tristan !!! Signez  cette  pétition  et  aidez-nous  à  convaincre  l’administration  belge  de  donner  enfin  à Tristan, après des années de combat, l’accès aux traitements qui lui sauveront la vie. Soutenez publiquement Tristan et partagez la petition afin d’obtenir une réponse positive de l’Office des Etrangers sur le dossier en cours, grâce à votre soutien Tristan pourra vivre jusqu’à l’âge adulte comme tous les autres. Tristan garde espoir, nous sommes de tout coeur avec toi! Pour plus d'informations, rejoignez-nous sur Facebook: https://www.facebook.com/Help-Save-Tristan-673781576143041/  Twitter: @SaveTristan-https://twitter.com/SaveTristan #savetristan  ASBL Alice www.alice.be  ---------------------------------------------- Help save Tristan’s life (English Version)  Purpose:   Obtain from the Belgian authorities the right for the little Tristan to remain on treatment in Belgium, since his Syndrome almost cost him his life. Tristan suffers from a very rare genetic condition (Russell Silver Syndrome) that cannot be treated properly in Rwanda, his country of origin. Petition summary: From birth, Tristan suffers from Russell Silver Syndrome. This condition threatens his childhood. He is very small for his age, suffers from multiple complications linked to the disease: body asymmetry, severe asthma with multiple crises, extremely oral and feeding difficulties, failure to grow and thrive, teeth implantation issues, the list is very long... Let's just say life hasn't been easy for Tristan & it's different compared to boys his age. Since his arrival in Belgium in  2014, Tristan has been hospitalized numerous times (emergency care at home and at the hospital linked to major hypoglycemia,  respiratory difficulties, asthma crises, IV feeding, general weakness, and surgeries). In December 2015, when Tristan was 4, and while he was about to head for school a major seizure happened,  this would have been fatal,  may it had happened during his sleep at night (comments from his endocrinologist of HUDERF Hospital Brussels after the ambulance crew saved his life). Tristan’s dad has put up a solid case supported by worldwide recognized experts and doctors: Dr. Harbison: Mount Sinaï Hospital, New York USA; Pr. Netchine from Trousseau hospital Paris, France, Belgian doctors from HUDERF and by Advisor MD of the Belgian embassy in Rwanda. They all have concluded that Tristan's life is at risk!– all records are available on demand In spite of all official comments and reports made by Doctors and specialist previously mentioned, the Belgian authorities and administration “The Belgium Immigration Office” and its medical appointed MD advisor do not understand and accept the necessity for Tristan to remain on treatment in Belgium. The administrative and legal processes in Belgium were made in due time and abiding by the local regulation and official processes. However, the Belgian administration is not following up anymore on the case, leaving Tristan in a real deadlock.  Today, in Rwanda he does not have access to highly specialized medical expertise, hormonal treatment (Growth Hormone notably) and general multidisciplinary care. Tristan's father is optimistic that in the near future Rwanda will surely have the necessary infrastructure to treat Tristan's rare syndrome, but Tristan's life is in danger now & we need to act! Conclusion Let’s share life with Tristan! Sign this petition and help us convince the  Belgian administration  (“Immigration Office”)  to give Tristan, after years of pain and suffering, the official papers to remain on the treatment that will save his life. Support Tristan publicly, share his story to get a  positive answer from the Belgium administration &  thank you in advance for your support. We are behind you, Tristan! For more info  join us on Facebook: https://www.facebook.com/Help-Save-Tristan-673781576143041/  Twitter: @SaveTristan-https://twitter.com/SaveTristan #savetristan  Asbl Alice www.alice.be ------------------------------ Help ons het leven van kleine Tristan te redden(Nederlandse Versie) Onderwerp van de petitie:  De  regularisatie  voor  kleine  Tristan  te  bekomen  want  zijn  zeldzame  genetische  afwijking heeft  hem  bijna  het  leven  gekost  –  Tristan  heeft  een  medische  behandeling  en  volledige opvolging nodig aangepast aan zijn pathologie. Dit is niet mogelijk in zijn land van herkomst. Samenvatting van de petitie Sinds zijn geboorte  lijdt Tristan aan het Silver-Russell syndroom; dit syndroom bedreigt zijn kinderjaren en zijn leven. Hij is zeer klein voor zijn leeftijd en  kampt met vele andere complicaties veroorzaakt door zijn  ziekte:  veelvuldige  hospitalisaties  vanwege  ernstige  ademstoornissen,  totale hypoglycemie, algemene zwakte, een kleine  gestalte en laag  gewicht.  Desondanks blijft  hij toch aanstekelijk optimistisch. Het meest zorgwekkende is echter de moeilijkheid om zich te voeden,  chronische  astma,  urologische  problemen,  lichamelijke  assymmetrie,  slechte gebitinplanting, de lijst is zeer lang… Samengevat  stellen  we  vast  dat  zijn  leven  allesbehalve  eenvoudig  verloopt  en  helemaal anders dan andere kinderen van zijn leeftijd. Sinds  zijn  aankomst  in  België  in  2014  is  Tristan  meermaals  per  ambulance  naar spoedgevallen vervoerd met symptomen van totale hypoglycemie, ademstoornissen, astma-aanvallen en totale uitputting  om  dan  behandeld  te  worden  met  intravenuese voeding  en chirurgische ingrepen. In december 2015, op 4-jarige leeftijd, net voor hij naar school zou gaan, heeft Tristan een ernstige aanval van stuiptrekkingen gehad die hem het leven had kunnen kosten indien dit tijdens zijn slaap zou zijn voorgevallen (volgens zijn endocrinoloog van het Kinderhospitaal te Brussel (UKZKF). Dit is helaas het dagelijks leven van kleine Tristan en zijn vader.  Het  medisch  dossier  dat  de  papa  van  Tristan  heeft  opgesteld  wordt  ondersteund  door  de grootste wereldspecialisten inzake de ziekte (Dr.Harbison, Sinaï-Hospitaal van New York en Dr.Prof.Netchine van  het  Trousseau-Hospitaal van  Parijs ; Belgische dokters  met  naam  van het  Koningin  Fabiola  Hospitaal  te  Brussel,  en  de  adviserende  dokter  van  de  Belgische Ambassade te Rwanda) – de verslagen zijn verkrijgbaar op aanvraag. Hij heeft bovendien de juridische procedure gevolgd om permanente medische behandeling te  kunnen  krijgen  in  België ;  helaas  geeft  de  Belgische  administratie  geen  gehoor  aan  de aanvraag  en  zelfs  een  bevel  tot  verlaten  van  het  Belgisch  grondgebied  gestuurd,  hetgeen momenteel wordt aangevochten sinds 2015, totnogtoe zonder enig antwoord. Ondanks  de  vele  medische  rapporten  opgesteld  door  befaamde  dokters  die  klaar  en duidelijk  hebben  vermeld  dat  « zonder  aangepaste  medische  behandeling  en  opvolging iedere banale infectie kan leiden tot een vitale prognose." De  Belgische  administratie  (Dienst  Vreemdelingenzaken :  DVZ)  en  hun  adviserende  arts erkennen de noodzakelijkheid tot een verblijf in België niet, ondanks afdoende bewijs van een  niet-voorhanden  behandeling  (behandeling  met  groeihormonen),  onvoldoende opvolging  (multidisciplinaire  teams  die  de  ziekte  kunnen  behandelen)  en  ontoereikende sanitaire toestand in zijn land van herkomst, Rwanda.  Conclusie Geef een plaatstje aan kleine Tristan !!! Door deze petitie te tekenen help je de Belgische administratie te overtuigen om eindelijk aan Tristan, na jaren van afzien, toegang te geven tot de behandelingen die hem het leven zullen redden. Ondersteun  Tristan  openlijk  om  een  positief  antwoord  te  krijgen  van  de  Dienst Vreemdelingenzaken ivm het aanhangige dossier. Dankzij uw steun zal Tristan kunnen leven tot op een volwassen leeftijd zoals alle andere kinderen. Help ons het leven van Tristan te redden!  ASBL/VZW Alice www.alice.be

Asbl Alice
3,183 supporters
Update posted 3 days ago

Petition to State Bar of Texas

Stop Attorney Nona Matthews from Harming Children in Our Justice System

En el fondo es en Espanol...   Above you will see a picture of Attorney, Ms. Nona Matthews. Our 12 year old son was the victim of her flagrant abuse and egregious decisions four years ago and he continues to be victimized by Ms. Nona Matthews for flagrant abuse of law.  Texas Attorney, Nona Matthews (Bar Code 00787982), represents school districts in the state of Texas regarding issues arising from the mistreatment of disabled students across the state. IMPORTANT: THE MAJORITY OF THIS ACTIVITY HAPPENED UNDER HEAVY SEAL IN THE LOWER FEDERAL COURT. JUDGE JOHN MCBRYDE DID NOT EVEN ALLOW THE FAMILY (CASE PARTICIPANTS) ACCESS TO THEIR OWN COMPLAINT. IT WASN'T UNTIL WE GOT TO 5TH CIRCUIT THAT WE COULD SEE ALL OF NONA MATTHEWS' ILLEGAL ACTIVITY.  She is well known for being extremely unethical in redacting factual information from records to cover the truth. She is doing this under deception of using the Family Educational Rights and Privacy Act also known as the acronym FERPA. The Act was created to conceal the child's identifiable information and NOT to be used to conceal the actual facts crucial to the knowledge of events in the judicial system. Redacting and covering those facts in records is unethical and does not allow justice to be served. It is deception. Nona also TAMPERS with evidence and changes government documents, blatantly lies and commits subornation of perjury. In Federal Court, she did much of this under heavy seal that even the family (case participants) were not allowed to access her illegal activity until well after the fact. This is all a fun game to NONA MATTHEWS - what's worse is that she intentionally and deliberately did this as a FACT WITNESS and decision maker to a disabled child harming a child permanently.   A good case is fought by the laws that protect the school districts, not by unethical acts Ms. Nona Matthews takes in hiding the truth ultimately harming disabled children and the judicial process further that is to fairly protect all as our legal system was intended to do.  Presently, we have a case in our legal system that she is doing much of the same to the ultimate harm of our minor young son that has continually been harmed by her tactics including making intentionally CRUEL and FALSE allegations in her briefs. It is deplorable and preventing justice from taking place. Ms. Nona Matthews also redacted facts that we took to the Hurst-Euless-Bedford School District School Board Grievance against the school district's Vice Principal Damon Emery for committing perjury in a Texas Education Agency Hearing also known as TEA. Ms. Nona Matthews redacted facts in order that the school board was not able to see what actually took place. Her acts have prevented justice from being served in the legal court system as well and she continues to do these extremely unethical acts to the detriment of many Disabled children across the state of Texas and to the detriment of justice being served. She has done this in legal filings in the court system as well. This is one of many very unethical acts she has taken in the TEA Hearings and the U.S. Court system including intentionally misrepresenting facts as she biasly protects herself for poor decisions she made. A good attorney fights with good caselaw and the laws set up by our country to protect the rights of all people with a fair, ethical, unbiased court proceeding. Harming children with these unethical acts is inexcusable and deplorable. These unethical acts have harmed Autistic children, children with ADHD and other learning disabilities in the schools across the state of Texas.  Additionally, Ms. Nona Matthews has also intervened with the Texas Education Agency Investigation team by asking certain TEA employees not to investigate complaints brought by parents for the safety of their children. She is doing this to protect her own bad decisions as well as unethically intervening with the Texas Education Agency investigations that are to protect children and teachers both. We ask that the process is allowed to go through without Ms. Nona Matthews unethical interventions.  We ask that Ms. Nona Matthews be fully investigated and disbarred for flagrant abuse of the law.  She has made thousands of dollars winning cases illegally. There are many that can attest to this as you will see in the comment section of this petition. Please sign our petition to help have Ms. Nona Matthews removed from the judicial system to prevent her from further harming Texas DISABLED CHILDREN and the legal system from doing the work it was intended to do to bring fair, ethical justice for all.   PETITIONING FOR CHANGE AND PLAYING FOR CHANGE!  Please sign this petition with ONE click on behalf of our son and all children's disability rights...we NEED Change for these children!!   IF YOU ARE NEW TO THIS PETITION, PLEASE READ THROUGH THE UPDATES.    Arriba veran un foto de la abogada Sra. Nona Matthews.  Nuesto hijo de 12 años fue la victica de su flagrante abuso y de sus decisiones atroces de hace cuatro años y el continua siendo victimizado por la Sra. Nona Matthews por su atroz abuso de la ley.  La abogada de Texas, Nona Matthews (numbero de barra de abogados 00787982). IMPORTANTE;  LA MAYORIA DE ESTA ACTIVIDAD SE LLEVO A CABO BAJO CIERRE INTENSIVO (LOS EXPEDIENTES NO ESTAN DISPONIBLES AL PUBLICO) EN LA CORTE BAJA FEDERAL.  EL JUEZ JOHN MCBRYDE NO LE PERMITIO EL ACCESO A LOS EXPEDIENTES NI SIQUIERA A LA FAMILIA.  ESTO ACERCA DE SU (DE LA FAMILIA) PROPIA QUEJA!  NO FUE SINO HASTA QUE LLEGAMOS AL CIRCUITO QUINTO QUE PUDIEMOS VER TODA LA ACTIVIDAD ILEGAL DE NONA MATTHEWS. Ella es muy bien conocida por su falta extrema de etica al redactar informacion objetiva de expedientes que abarquen la verdad.  Ella esta haciendo esto bajo engaño al usar  el Acta de los Derechos Educacionales y de Privacidad tambien conocida for sus siglas en Ingles FERPA.  El acta fue creada para sellar (mantener inaccesible) la informacion identificable del niño y NO para ser usada para sellar (esconder) los propios hecho cruciales para tener conocimiento de los eventos en el sistema judicial.  Redactando y encubriendo esos hecho en los expedientes carece de etica y no permite que se haga justicia.  Es un engaño. Nona tambien altera (falsifica) la evidencia y cambia documentos del gobierno, descaradamente miente e instiga a cometer perjurio.  En la corte federal hizo mucho de esta bajo sello (con expedientes que no son accesibles) que ahun la family (participantes del caso) no se les dio acceso a su actividad ilegal sino hasta mucho despues de los hechos.  Todo esto es un juego divertido para NONA MATTHEWS - lo peor es que ella intencionalmente y a proposito hizo esto siendo un TESTIGO DE LOS HECHOS y siendo una de las personas que tomarian una decision respecto a un niño con una discapacidad, dañando al niño permanentemente. Un buen caso (a favor de un niño) es combatido por las leyes que protegen a los distritos escolares y no deberian ser combatiodos con hechos sin etica de la Sra. Nona Matthews quien oculta la verdad y a final de cuentas daña a niños discapacitados y al proceso judicial cuyo objetivo es proteger justamente a todos.  Hoy en dia, tenemos un caso en nuestro sistema legal al cual ella le esta haciendo mucho de lo mismo lo cual, a final de cuentas, termina dañando a nuestro hijo menor quien ha sido continuamente lastimado por las tacticas de ella, inclyendo haciendo alegatos FALSOS y CRUELES en sus informes.  Esto es deplorable y esta previniendo que se haga justicia. La Sra. Nona Matthews tambien redaca hecho que llevamos a junta de quejas del distrito escolar Hurst-Euless-Bedfors en contra de el vice presidente de la escuela Damon Emery por cometer perjurio en una audiencia de la Agencia de Educacion de Texas tambiien conocida como TEA por sus siglas en Ingles.  La Sra. Nona Matthews redacto los hechos de tal manera que la junta escolar no pudiera ver lo que realmente estaba pasando.  Sus acciones previnieron que se hiciera justicia en el sistema legal de las cortes y ekka tanbueb continua cometiendo estos hechos extremadamente sin etica que perjudican a muchos niños discapacitados por todo el estado de Texas y que no permiten que se haga justicia.  Ella tambien ha echo esto en presentaciones legales en el sistema de cortes.  Este es uno de los muchos hechos con mucha falta de etica que ella ha llevado a audiencias de la TEA en el sistema de cortes de Estados Unidos incluyendo tergiversar hechos para protegerse a si misma, con prejuicio y parcialidad, de las pobres decisiones que ha echo. Una buena abogada pelea con casos de ley y con las leyes que se establecieron en nuestro pais para protejer los derechos de todas las personas con un procedimiento en corte justo, etico e imparcial.  Dañar a los niños con estos actos sin etica es imperdonable y deplorable.  Estos echos sin etica han lastimato a niños autistas, niños con ADHD (THDA, trastorno de hyperactividad con deficit de atencion) y otras discapacidades de aprendizaje en escuelas por todod el estado de Texas.  Adicionalmente, la Sra. Nona Matthews ha intervenido con empleados del equipo de investigacion de la Agencia de Educacion de Texas al pedirles a ciertos empleados que no investiuen quejas que los padres han interpuesto con respecto a la seguridad de sus hijos. Ella hace esto para proteger sus propias malas decisiones y tambien su intervencion sin etica con las investigaciones de la Agencia de Educacion de Texas. Teles investigaciones son para proteger a los niños y a los maestros. Pedimos que el proceso se le permita continuar sin las intervenciones sin etica de la Sra. Nona Matthews Pedimos que la Sra. Nona Matthews sea completamente investigada y sea expulsada de la abogacia for su flagrante abuso de la ley. Ella ha ganado miles de dolares ganando casos ilegalmente. Hay muchas personas que pueden atestiguar sobre esto como veran en la seccion de comentarios de la peticion. Por favor firmen nuestra peticion para ayudar a que remuevan a la Sra. Nona Matthews del sistema judicial y para detenerla de que continue dañando a NIÑOS DISCAPACITADOS en Texas y parar que siga previniendo que el sistema legal funcione en la forma para la que fue diseñado: que haga un trabajo justo, etico y con justicia para todos. HACIENDO UNA PETICION POR UN CAMBIO Y ORANDO POR UN CAMBIO. Por favor firmes la peticion con un 'click' de parte de nuestro hijo y todod los derechos de niños con dicapacidades...NECESITAMOS un cambio para esto niños. SI ESTA PETICION ES NUEVA PARA TI POR FAVOR PONTE AL DIA LEYENDO TODAS LA ACTUALIZACIONES (UPDATES).                             Esta peticion sera entregada a: La Barra de Abogados de Texas

Kristie Cripps
126 supporters