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Helping Others To Freedom Pt10: Revival And Deliverance - The Bigger Picture

In the concluding session of 'Helping Others To Freedom', we look at how the principles of personal healing and deliverance apply to whole regions, and are essentially the same principles that can prepare a region for revival awakening. This is 'Revival And Deliverance - The Bigger Picture' - God sets individuals free in order to heal and deliver the world. This session is available at https://www.preachtheword.com now in MP3 audio format and in HD video on our YouTube Channel (https://youtube.com/PreachTheWord)...



  • Religion & Spirituality

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Jesus' Preparation For Ministry Pt1: From Obscurity To Prominence

There is much of Jesus' early life we don't know about. We know He didn't begin His earthly ministry until around the age of 30. What did He do in those preceding years? Those years in obscurity were a vital part of 'Jesus' Preparation For Ministry'. What lessons can we learn from such obscurity and silent years? Follow Him 'From Obscurity To Prominence', as we consider this question and also the importance of Christ's baptism, holiness, obedience and His empowerment by the Spirit. This message is available at https://www.preachtheword.com now in MP3 audio format and in HD video on our YouTube Channel (https://youtube.com/PreachTheWord)...



  • Religion & Spirituality

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The Prayer Of Jabez

The short but direct 'Prayer Of Jabez' has been a blessing to many who have plumbed its spiritual depths and excavated its potential. Explore with us how God wants to bless us, deliver us from everything holding us in the past, enlarge our Kingdom influence and grant our petitions for His glory. This message is available at https://www.preachtheword.com now in MP3 audio format...



  • Religion & Spirituality

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Questions About Healing, Faith And Unbelief

In this message on Matthew 17:14-21, David addresses some critical questions about healing and what the Bible says. Some may object to any emphasis on healing as a distraction from the gospel's central message. However, the record of the Gospels and the Acts is that healing was intrinsic to Jesus' revelation of the Father to humanity. In this teaching, learn how faith affects healing and how our unbelief can affect our faith. This message is available at https://www.preachtheword.com now in MP3 audio format...



  • Religion & Spirituality

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Don't Fear, Only Believe

In this story of two overlapping healings - the woman with the issue of blood and the raising of Jairus' daughter - we learn some principles of how God heals. Sometimes, we can be confused about how God does His healing work. In this account, Jesus emphasises the importance of saying 'No' to fear and only believing what God has said. Don't fear, only believe! This message is available at https://www.preachtheword.com now in MP3 audio format...



  • Religion & Spirituality

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Which Report Have You Believed?

Whose message are we listening to? Whose report are we believing? The press, social media, medicine, or Gods Word? What voices are we allowing to influence us, and are those voices faith-inducing or faith-reducing? Isaiah 53 is such a well-known scripture about the death of Jesus and the salvation He has purchased for us. But many have neglected that this core prophetic scripture is explicit that healing has been purchased for us at the cross of Jesus. Learn what Isaiah 53 truly teaches and then ask, 'Do you believe this report?' or, whose report are you believing? This message is available at https://www.preachtheword.com now in MP3 audio format...



  • Religion & Spirituality

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Help My Unbelief

Mark's record of this miracle in Mark 9:14-29 is different in some ways to Matthew's account. One very significant difference is how the father of the afflicted boy confessed his faith in Jesus' ability to heal; but he also admitted that he had unbelief in his heart too. There are many lessons to learn in this story concerning what demonic affliction can do to someone, even from childhood, and how Jesus ultimately set the boy free. However, we see one very encouraging truth in particular: though the boy's father's faith was imperfect, Jesus still honoured it and healed the boy. God answers even imperfect faith. This message is available at https://www.preachtheword.com now in MP3 audio format...



  • Religion & Spirituality

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Antonio Resines Recibe el Premio de Honor en el IV Festival Internacional de Cine de Hellín

El IV Festival Internacional de Cine de Hellín (FECHE) se prepara para tomar el centro del escenario cultural del 16 al 22 de noviembre, convirtiéndose en un faro de actividades cinematográficas en la provincia de Albacete. Con una oferta que va más allá de las proyecciones de cine, el festival promete días repletos de cultura […]

Artículo publicado en : Antonio Resines Recibe el Premio de Honor en el IV Festival Internacional de Cine de Hellín




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Globalcaja Destina 250.000 Euros a Familias de Letur y Mira Afectadas por la DANA a través de Servicios Sociales

En un esfuerzo conjunto para mitigar los efectos devastadores de la reciente DANA que golpeó las localidades de Letur en Albacete y Mira en Cuenca, Globalcaja ha destinado un fondo de 250.000 euros que será gestionado por los Servicios Sociales de Atención Primaria de Castilla-La Mancha. Esta ayuda económica será repartida equitativamente entre ambas localidades […]

Artículo publicado en : Globalcaja Destina 250.000 Euros a Familias de Letur y Mira Afectadas por la DANA a través de Servicios Sociales




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Page Propondrá Agenda de Armonización para Mejorar Colaboración Autonómica Tras Emergencia

El presidente de Castilla-La Mancha, Emiliano García-Page, ha manifestado su deseo de proponer al gobierno central una agenda clara destinada a mejorar la colaboración institucional con las comunidades autónomas. Este anuncio se realizó durante la firma de convenios con la Universidad de Castilla-La Mancha y la Universidad de Alcalá, en la que García-Page abordó la […]

Artículo publicado en : Page Propondrá Agenda de Armonización para Mejorar Colaboración Autonómica Tras Emergencia




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Atender a Familias Vulnerables y Recuperar Servicios Esenciales: Prioridades en Mira Tras la DANA

La alcaldesa de Mira, Miriam Lava, ha tomado cartas en el asunto tras la devastación causada por la reciente DANA que afectó gravemente a su municipio. En un esfuerzo por mitigar el impacto sufrido por las familias vulnerables, muchas de ellas de nacionalidad rumana, Lava ha firmado un Protocolo de Colaboración en Emergencia con la […]

Artículo publicado en : Atender a Familias Vulnerables y Recuperar Servicios Esenciales: Prioridades en Mira Tras la DANA




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Transformación Gastronómica: Antiguo Convento de Las Terreras en Ciudad Real Recibe 1,5 Millones en Inversión

El emblemático convento de la Inmaculada Concepción de Ciudad Real, conocido como el convento de las Terreras, se prepara para una transformación significativa que lo convertirá en un centro de interpretación dedicado a la gastronomía manchega. Esta ambiciosa iniciativa, que busca revitalizar el patrimonio cultural de la ciudad, cuenta con una inversión de 1,5 millones […]

Artículo publicado en : Transformación Gastronómica: Antiguo Convento de Las Terreras en Ciudad Real Recibe 1,5 Millones en Inversión




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El Gobierno Regional Paga 22,5 Millones de Euros a Agricultores Conquenses por Ayudas de la PAC

El sector agrícola y ganadero de la provincia de Cuenca ha recibido un significativo respaldo económico por parte del Gobierno regional, que ha procedido al pago del anticipo de los ecorregímenes de la Política Agraria Común (PAC) 2024. El delegado provincial de Agricultura, Ganadería y Desarrollo Rural, Rodrigo Fernández Alcalde, ha anunciado que se han […]

Artículo publicado en : El Gobierno Regional Paga 22,5 Millones de Euros a Agricultores Conquenses por Ayudas de la PAC




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El Gobierno de Castilla-La Mancha Resalta el Legado de Manuel Marín en la Construcción Democrática de Europa

Ciudad Real, 12 de noviembre de 2024.- El Gobierno de Castilla-La Mancha ha rendido homenaje a Manuel Marín, destacando su papel esencial en la construcción de una Europa democrática y cohesionada. Este reconocimiento fue manifestado por Nazaret Rodrigo, directora general de Asuntos Europeos, durante la presentación del libro ‘Raíz y Rama. Un homenaje a Manuel […]

Artículo publicado en : El Gobierno de Castilla-La Mancha Resalta el Legado de Manuel Marín en la Construcción Democrática de Europa




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Ciudad Real Se Prepara Para Implementar La Zona De Bajas Emisiones Que Optimizará El Aire Y La Movilidad

El Ayuntamiento de Ciudad Real está reconsiderando el calendario para la implantación de la zona de bajas emisiones (ZBE) en la ciudad. Esta decisión responde a la necesidad de llevar a cabo un exhaustivo estudio jurídico del borrador de la ordenanza elaborada por la Concejalía de Movilidad. El objetivo es evitar «problemas jurídicos» como los […]

Artículo publicado en : Ciudad Real Se Prepara Para Implementar La Zona De Bajas Emisiones Que Optimizará El Aire Y La Movilidad




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Izquierda Unida C-LM Establece Abril de 2026 Como Fecha Límite para Definir su Estrategia Electoral para los Comicios Autonómicos y Municipales

Izquierda Unida de Castilla-La Mancha ha fijado abril de 2026 como la fecha límite para presentar sus candidaturas para las elecciones autonómicas y regionales de mayo de 2027. Así lo ha anunciado Pedro Mellado, el coordinador general de la formación, en una reciente entrevista. Mellado destacó el compromiso de IU de informar con un año […]

Artículo publicado en : Izquierda Unida C-LM Establece Abril de 2026 Como Fecha Límite para Definir su Estrategia Electoral para los Comicios Autonómicos y Municipales




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Page Celebra la Creación del Alto Comisionado y Exige al Estado Compromiso en la Restauración de los Cauces

El presidente de Castilla-La Mancha, Emiliano García-Page, ha mostrado su satisfacción por la decisión del Gobierno central de crear un Alto Comisionado destinado a agilizar la reconstrucción en las zonas afectadas por la reciente DANA (Depresión Aislada en Niveles Altos). Durante un discurso en Puertollano, García-Page expresó su confianza en que la Administración central no […]

Artículo publicado en : Page Celebra la Creación del Alto Comisionado y Exige al Estado Compromiso en la Restauración de los Cauces




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Invest in Bogota Presenta Agenda de Trabajo en Web Summit de Portugal para Atraer Inversionistas

Este lunes comenzó el Web Summit en Lisboa, Portugal, uno de los congresos de tecnología más destacados a nivel global. Con la participación de más de 3.000 empresas de 160 países y la asistencia de más de 1.000 inversores, el evento se perfila como un epicentro para el sector tecnológico mundial, reuniendo a un público […]

Artículo publicado en : Invest in Bogota Presenta Agenda de Trabajo en Web Summit de Portugal para Atraer Inversionistas




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Twas the Night Before Christmas by Lobotomy Boy

It's Christmas and Lobotomy Boy has a special version of "The Night Before Christmas" for everyone!

Enjoy this special Holiday Edition of Bedtime Stories My Kids Love.



MP3 File - Click Here to Download Podcast




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Adventures of Man in the Can - Ch 14 - The Great Exodus - No One Left Behind



The destruction of the park has begun!! The Man in the Can quickly realizes a family of squirrels is in the mist of the mayhem. Can Yellow Bird and Man in the Can save the family?

Find out in this episode of The Adventures of the Man in the Can.



MP3 File - Click Here to Download Podcast




GREAT DEALS FOR LISTENERS! CLICK BELOW
!


Save 10% on all your pet's needs at PetMeds.com
Up to 20% off on great athletic gear at Eastbay.com
Save 15% on your favorite stuff at Footlocker.com
Save 20% on your flower order with FTD Fluerop.com
Save $10 off your next order from PetCareRX.com





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Where is My Big Toe















The Ghoul is out of the Graveyard and tells a terrifying tale of a missing big toe! Hear this terrifying tale on today's Bedtime Stories My Kids Love.

Enjoy our special October edition of Bedtime Stories My Kids Love.



MP3 File - Click Here to Download Podcast





GREAT DEALS FOR LISTENERS! CLICK BELOW
!




Save 20% on your flower order with FTD Fluerop.com
Save $10 off your next order from PetCareRX.com




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Brothers and Sisters

A friend posted this quote earlier today on Facebook and I had to borrow it.

"To the outside world we all grow old. But not to brothers and sisters. We know each other as we always were. We know each other's hearts. We share private family jokes. We remember family feuds and secrets, family griefs and joys. We live outside the touch of time."
 -Clara Ortega 

Our children are all still young but it made me go back and look at the past 9 years. Here's what I found:






















So very thankful they have each other.








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Baby Seven

Well, I'm bringing the blog back to announce that we are expecting baby seven in October! I think most everyone who reads this blog already knows this, however, since this is mainly a scrapbook for our children, it seemed fitting to write this post. We are thrilled and so thankful for our new little baby. All of the children are so excited and ask daily when we will find out if this baby is a boy or a girl. :) Hopefully, we will find out ON MONDAY! :) I'm having an early ultrasound done and if the baby cooperates, we will know then!

I've mentioned before that the baby's heart rate at 14 weeks has correctly determined the gender of every one of our children. The girls' heart rates were both in the 170s and the boys' were all in the 150s. Well, I had my 14 week appointment today and the heart rate was 138! I'm going to assume that means BOY.
Another interesting predictor for us has been the year in which the baby is born. The girls were both born in even years and the boys were born in odd years. This is an even year so that suggests a GIRL. So, we're back to square one with the predictions. Maybe we will know on Monday. I'll come back with the results then.

Here's a picture of seven at 10 weeks:




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Baby Seven is....

a BOY!!!! We were all able to go to the ultrasound today, which is a first. Normally just Rick and I go but this time everyone tagged along. The room was huge and it had a few toys in in for the children to play with. Jack and Sims played with those toys the entire time. Miles sat with Rick and looked confused, and Kate, Claire, and Henry seemed pretty interested to see what was going on. The tech asked for last minute guesses and all of the kids guessed GIRL. We could tell right away that he was in fact, a HE and everyone was happy - even Kate and Claire. :)
We are thrilled to know and thankful to be having another little boy. That will make 5 boys, 6 and under! How fun will that be?? We will have our own boys' basketball team. It's a good thing I have Kate and Claire - they will help soften up our home. :)
We are praying the Lord will continue to knit him together and that we will be able to meet him in time.




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Where have we been?

Let's see, in the past 3 months, we:

1. Finished soccer season
2. Had 3 ballet recitals
3. Took the kids on a SURPRISE trip in Disney World
4. moved to a new city 50 miles away (4 days after we returned home from Disney)
5. unpacked our new home
6. drove back and forth between new and old home to get old home ready to rent out.
7. paid $$$$$$$$$$$$$ for a new A/C unit at our old home
8. started some of our schoolwork

So, we've been just a little busy. We have now finished our work on the old house so we're hoping things will start to calm down just a bit.

I'm currently 26 weeks and feeling good. I am starting to get heartburn at night occasionally, but it's not that bad yet. I cannot believe it's almost the 3rd trimester-this pregnancy has completely flown by. Hutch 7.0 still is nameless but hopefully not for long. I go back to the doctor the first week of August and then it's every 2 weeks until 35 weeks where I'll go weekly. Time tends to speed up at this point until about 36 weeks when it slows WAY down. I'll be interested to see how these last months go this time.

My next post (hopefully tomorrow) is going to be our new school curriculum/year.


On one of our many trips to Home Depot/Lowes :) Good thing we have a lot of helpers. 
 




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Pictures from the Park - November 2014

We went to the park back in November to enjoy the nice weather and because Rick took the day off of work. This is one of my new favorite pictures of the kids. Little Luke (exactly 1 month old at the time) was in his little car seat. Maybe he can climb on the slide with everyone this summer. :)


Claire - 8, Miles - 22 months, Kate - 9, Sims - 3

Kate and Miles

Jack - 4

Sims, Jack, Henry - 6, Miles, Kate, Luke - 4 weeks, Claire

Claire and Kate




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Breech baby, breech baby

I am nearly 37 weeks now and baby Charlotte is still breech. She has been for as long as I can tell. I feel kicks in totally different places than I normally do and I'm not experiencing some of the late term pains that the others have given me. I think she just likes being up close to my heart. :) I will be admitted to Labor and Delivery early Wednesday morning and my doctors will attempt to manually turn her. Claire was also breech and I had the same procedure preformed with her. Since Charlotte and Claire have the same initials, I'm just assuming she's trying to be like her big sister.


Honestly, the procedure hurts - a lot. Two men stand on either side of you and basically pick the baby up and push to get her in the right position. It hurts - a lot - did I mention that? However, it is fairly quick and they can immediately tell if it is going to work. Either way, we will both be monitored during and after for signs of stress. If need be, an emergency Csection will be done but my doctor has never had to do that. If successful, we will then wait a few more weeks until she is ready to be born. If unsuccessful, we will schedule a Csection for 39 weeks. 

It might be a quick update but I will post again on Wednesday as to whether or not she turned for us. 




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Well, she flipped back.

I just returned home from seeing the doctor and sweet baby girl has flipped again. I guess she just likes being breech. So, we have decided it's best to have a csection. There were many factors I discussed with my doctor before making this decision. He delivered every single one of our kids and I'm so glad it appears that he will also be taking care of Miss Charlotte. We have our date and, Lord willing, she will be here end of next week. Hopefully, the next post will have a picture of our new little one!




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Charlotte's Birth Story

Things to know before reading:

1. Charlotte was breech
2. I had a version preformed to flip her
3. She flipped back


When I last left off, I was waiting on our planned c-section. I had a list of things to do and by the Thursday before her Saturday arrival, nearly everything was finished. All of our school work for the semester was complete and all of the laundry in my house was washed, folded, and put away. The only major family thing I had left to do was packing. I never got around to packing.

Thursday afternoon I noticed I was having about 4 contractions an hour. I paid no attention to these because in my previous pregnancies, I had weeks and weeks of contractions prior to actual labor. This pregnancy, I had NO "practice" contractions. I just assumed it was because she was breech and so there was nothing to get ready for. My cervix was also closed at every appointment in the last weeks which is also not normal for me. I normally am between 3-4 cm before I go into labor. So back to the few contractions, I just assumed these where the ones I had been without for the last 6 weeks.

I started cooking dinner on Thursday night and got about halfway through cooking when I felt the first painful and long contraction. It was at 5:15. From that point on, they were coming every 2-3 mins without stopping and lasting over a minute. They went from 0-60 immediately. I couldn't finish making dinner so I really have no idea what the kids ate that night. Rick walked in the door at 6 and I asked him to take Kate to dance and take all of the other kids with him. He asked if it was "time" and I said, "No, I just need to try and make them stop." I had 2 times with Luke where I had similar contractions prior to labor that lasted 2 hours and then stopped. I was assuming that's what was going on here. So from 5:15-9:15, I walked around my house, laid down in my bed, took 2 baths, but nothing was stopping them. It was the same pattern, 2-3 mins apart and lasting from 1-2 mins. I wasn't getting any relief or downtime in between contractions. At some point during this 4 hour period, Rick picked Kate up from dance, printed and folded the bulletins for Sunday, and took them to the church.

I told myself if they were still going at 9:15 that I would call my doctor. My doctor told me to come on in and get checked out and that they would probably keep me overnight to monitor me and decide what to do early Friday morning. I still wasn't sure if I was in labor or not and really didn't want to go and then get sent home so I was relieved that they were going to keep me and that Charlotte would probably be born the next day when my doctor was on call. (He delivered all 7 of our other kids.)

I texted my sister to come stay with the kids and started packing my bags. I always wondered why people packed their hospital bags early. I thought you would have plenty of time in between contractions to get what you needed. Haha! I ended up at the hospital with 6 shirts and 1 pair of shorts. :) I guess I really was in pain.

The ride to the hospital was horrible. Every bump magnified the pain. The contractions didn't slow down and that was when I finally realized that I was actually in labor. It took us about 45 minutes to get to the hospital. I think we arrived around 11:00pm and I was taken to triage to get things checked out. I had never actually been to triage so that was something new. They monitored me for an hour and I had to lay on my back that entire time. That was horrible. I'm pretty sure you are not meant to lay on your back without pain relief during labor. :) They also did an ultrasound to check her position and she was in fact, still breech.

Around 12:20am, Friday morning,  the doctor on call came in said it was time for Charlotte to be born and that we couldn't wait any longer. My contractions were not stopping and my cervix was opening.  From that point on, everything moved quickly and slowly at the same time. The anesthesiologist came in and said I would be getting a spinal because they couldn't wait for an epidural to work. He told me all of the side effects but I'm not really sure what he said. I had to sign about 20 pages of release forms and they I was wheeled off to the operating room while Rick waited in triage to be called back.

I remember the operating room being very, very bright and there were a lot of people in there - I think 10. I'm used to the quiet dark delivery rooms with just one nurse and the doctor so this was a change. I moved from the triage bed to the operating table and was given my spinal. I do remember the anesthesiologist saying that if the spinal didn't take for some reason that they would immediately knock me out and that when I would wake up I'd have a baby. I was hoping that didn't happen. He poked my arm with some kind of sharp object and then would poke on my stomach to make sure I didn't feel anything. The first 2 times he did it I felt it but by the third time, I couldn't feel anything. At that point Rick was let in the room and they began. They had been prepping and draping me during this time as well. Charlotte was born at 12:50 am. She was born toward the beginning of the surgery and it seemed that the bulk of the time was spent getting stitched back together.

She was immediately shown to me over my drape and then taken to get cleaned up a bit. About 2 minutes later she was brought over to me and placed on my chest and I held her for about 5 mins. She was then taken away (in the same room again) to be weighed, etc and Rick went with her. She was then brought back to me all bundled me for a few kisses and then Rick was able to carry her to the recovery room to wait for me. I was in the recovery room for 2 hours and during that time my parents came up to see her. I was able to nurse her which was great. I was also given a pump for my pain medication. The nurse sacred me because she told me to push the button every 8 mins and to stay on top of the pain. She warned me not to fall asleep because if I did and then woke up an hour later, I would not be able to handle the amount of pain I would be in. It was 2:00 in the morning and I was drugged up on morphine and she was telling me not to fall asleep! I guess it worked because I didn't sleep until later that morning, after the pump was turned off. :)

I was in love with her from the moment I saw her. My main concern with having a c-section, prior to having it, was that I would somehow feel like I missed out on the birthing process. I never felt that way. I carried her for 9 months and she arrived in the safest way possible for both of us. It was perfect. The only thing I was sad about was that my doctor missed delivering her by 5 hours. However, that was the Lord's will too. He was on call all weekend so he checked on me everyday while I was in the hospital. C-section recovery is painful. That's all I want to say about that. I just want to remember the hours and minutes before, during, and after her birth. I am thankful for every moment of it.









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Expose Your Blog.



Many of my readers will have probably first found my blog through the old blog traffic exchanges like Blog Explosion and Blogazoo, they were a good source of traffic for bloggers and increased readership, sadly those sites have all gone now.

But don't despair there is another Blog Only traffic exchange I've found, Expose your blog has a long timer so visitors definitely read your blog. There is currently a weekly referral and surfing contest too (see the sites forum for more details) so sign up now and start recruiting your blog readers.

If you've never heard of a traffic exchange before let me explain, you add your blog and once it's approved you surf "other peoples blogs reading each one for 30 seconds (or more if it grabs your attention) you then click a button to move onto the next blog and earn credits as you surf. The ratio on expose your blog seems tight at first but there are bonus credits that appear as banners and about every 10 pages theres a verification page where you earn bonus credits. If your looking for traffic to your blog it's a good place to start. Also make sure you remember to surf at least 5 blogs to activate your blog when you sign up, I recommend surfing more in fact to gain as many credits as possible.

For more advice on increasing blog traffic see my other post on the subject:

My Tips On Increasing Blog Traffic



  • blog traffic exchange
  • improve blog traffic
  • increase blog traffic
  • more blog hits

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Arthur Of Albion - Book Review



Arthur of Albion is a beautifully illustrated version of the King Arthur Stories for children, an excellent book for older boys (or girls) interested in Knights. Published by the wonderful Barefoot Books company.

It is set out as a sequence of stories told each night at the round table, as King Arthur requires one of his Knights to tell a tale of valor and adventure every knight before dinner.

It is written by John Matthews illustrated by painter Pavel Tatarnikov and is truly breathtaking, the hardcover edition comes with a map folded up in the back showing the lands of Albion (or the UK as we know it now) in the days these stories were first told.

It would make a fantastic gift for children who are confident readers or to be read aloud to younger children, The way the stories are told makes it an excellent book for reading aloud one story a night for example.

Arthur Of Albion Available on Amazon.


 




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Email Your local MP telling them to stop Cuts to support for disabled people.

38 Degrees appear to have finally started a campaign to put pressure on the government to stop cuts to support for disabled people. Click here to email Andrew Turner (or whoever your local MP is) it only takes a minute you just need to provide your postcode and fill in your address. MP's do respond to emails too I've had several letters from the house of commons in response to emails I've sent.




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Should We Blame ATOS?

Today I have read a blog post where the author basically suggests disability campaign groups are wrong to go after ATOS to the extent that they are, and that ATOS are only the IT company in charge of a system put in place by the DWP and they are the ones we should really be targetting. I've also seen several leading disability campaigners openly support this view, and even not support DPAC's protests at the Paralympics (which are being sponsored by ATOS).

I do agree with this argument to an extent, we do need to clearly target the people behind this assessment process, and not just ATOS. I thought we had been from day one though? We have constantly lobbied the government and named the ministers responsible for this crisis as well as targeting ATOS.

But the defense "we are only doing what the government/DWP is telling us to do" is an empty one in my view. Wasn't it also the defense many NAZI's also used when being tried after WW2 was over? "we were only obeying orders"? Recent documentaries that used secret filming have shown us that ATOS assessors are having crisis's of conscience over the process, they cope by blaming it on "the decision maker" (which sounds incredibly Orwellian to me). I think these individuals need to be made to take responsibility for their own actions, they could speak out even if it is anonymously, or they could quit their jobs and find another one. At least the NAZI's had the defense that they would have been executed if they disobeyed Hitler's orders, no one is going to shoot an ATOS assessor for walking out and saying "I can't do this anymore".

When a disabled person goes to one of these assessments their life and quality of life is in this persons hands, the decision maker makes their decision based on what box these people tick. In my case after examining the criteria I can clearly see 3 places my assessor should have awarded me points and failed to, and I appealing their decision. All I wanted was to be put in the work related activity group where I would receive the help and support I need to get back into work after 10 years of unemployment. Just one year to give me a fighting chance of finding a job I can reliably do with enough hours to support myself and some kind of support system that ensures I do not lose my job if I become ill again for a short period, and I would stick my middle finger up to the DWP and never claim again. But they did not give me that, they only awarded me 6 points, and I was lucky to get that by all accounts. I have the support to be able to make an appeal which I am confident I will win, but many others don't. Many people will not be able to act when they receive that dreadful letter saying they have been turned down for ESA, they will just sink into despair and lose everything, end up homeless and destitute. Some will harm themselves or even kill themselves alone, they may not be found for days or even months.

So I'm sorry but I say YES we should and must blame ATOS, we must blame everyone responsible for this horrific mess. If anything we need to focus more of our attention on the organ grinders and not the monkeys, but we must not give in and let up in our campaigns against ATOS to gain sympathy from the right wingers. We must continue to target every one of them, and not rest until they ALL are bought to justice.

 



  • ATOS
  • work capability assessment

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Ed Miliband's reply To Sonia Poulton.

I'm reading that lot of people seem to have taken a lot of negative things from Ed Miliband's reply to Sonia Poulton's letter regarding welfare reform and the new Work Capability Assessment that was signed by thousands of people including myself. I'm actually quite surprised by this as I thought for a letter from a Politician it was very positive and actually addressed what it said in the original letter directly, which is quite rare. Lets look at it again for a moment.

Dear Ms Poulton,
Thank you for your correspondence regarding the Work Capability Assessment, and my apologies for the delay in replying. Disabled people need support and compassion, and the Labour Party believes in a welfare state that fulfils this principle. The previous Conservative Government took the opposite approach and left many disabled people on Incapacity Benefit with little support to return to work where possible. It is also important to separate out ill health and disability from the decision not to work, which is taken by a distinct minority. For these reasons, the previous Labour Government introduced the Work Capability Assessment, and I am supportive of the principles behind this test.
However, I share some of the concerns that have been expressed about the test by you, along with many charities, disability groups and healthcare professionals.
These concerns, the high percentage of appeals, and Professor Malcolm Harrington’s expert reviews have shown that the test must be improved. The Government needs to listen to Professor Harrington’s advice, especially when his third review for 2012 comes out. 
We have also forced a vote in Parliament on the need to reduce the human cost of the wrong decisions that result from the WCA in its current form. Given the importance of this issue, I am keen that you discuss this further with the Labour Party and share with us some of the experiences of people going through the WCA that you have collected. Anne McGuire, my Shadow Minister for Disabled People, would be happy to arrange a meeting in order to do so. Please contact her on ********** to arrange a convenient time.
Thank you again for taking the time to get in touch on this issue.
Yours sincerely, Rt Hon Ed Miliband MP
I can see it's going to have been the first paragraph that has angered people so much, he is stating what the new WCA was meant to achieve there. I agree with the points he makes, there was little or no support for people wanting to return to work from incapacity benefit under the old system. I have always wanted to work and said that in every medical I ever had under the old system. The problem is that I have to have a job I can reliably do, and mental illness prevents me doing a lot of jobs.

The new system was supposed to support me to get back into work which I was pleased to hear, but when I finally had my assessment I was horrified to find they were trying to deny me ESA altogether. I was confident I would get into the work related activity group where I would still receive ESA for 1 year and attend groups and activities designed to help get back into work. I am now having to go through the stressful and uncertain process of appealing their decision, and I daily read about people who have severe physical disabilities or are even dying being declared fit to work.

If we lived in a Utopian society where every employer would pay for adaptations and carers for disabled people from their own profits to enable them to work, and every employer was trained in mental health issues and was sympathetic towards employees who suffer from them. If businesses could afford to employ people who may be absent because they are receiving medical treatment  or just too ill that day to show up, then it would work. Every disabled and mentally ill person would have a job and we'd all stand in a big circle with the able bodied and mentally well holding hands and sing "I'd like to teach the world to sing".

But here's the problem Ed, society is not like that, hate crimes against the disabled are being committed every day, employers can't afford to adapt buildings and employ carers without any funding available. And where are all these jobs we are supposed to be applying for anyway? There aren't even jobs for the able bodied who have just been made unemployed, let alone jobs for a woman like me who hasn't worked for 10 years because I'm mentally ill and prone to nervous breakdowns. And all the thousands of others who have even more severe metal illness's and physical disabilities, who is going to employ them Ed?

Even if I do make it to the Work Related Activity group, what will the people there actually be able to do for me to remedy these problems? Are the department for work and pensions even the best people to be in charge of such a thing? How are we going to change society enough in the one year I have to get me a job? There are thousands like me, nothing the DWP alone will be able to do will find us all suitable jobs. Money needs to be available to employers to enable them to employ us, and they need to be educated in the many and complicated needs of people who have mental illness and disabilities. More jobs need to be created to meet the demand for them, as we want to work Ed we really do, this minority of people who don't want to work are non existent Ed. Only someone who's never had to live on benefits would say something like that, it is a soul destroying experience and everything rests on the words of an anonymous decision maker who you will never meet.

So that's the bit that makes us angry fair enough, but he does go on to talk about the human cost of what is happening, so he's admitting things aren't right there in a veiled way. And he says that he has concerns about the high number of appeals, that's all we can really hope for, he's a politician after all. He's never going to turn around and just say "sorry everyone it's not working like it should have, we didn't think it through we'll go back to the drawing board", Politicians just don't do that. But there is hope that behind closed doors they are frantically reassessing what they've done and realising it is going horribly wrong. Bills have gone through parliament now though and thousands of people are suffering, if they admit they were wrong they will have to compensate everyone who has suffered, I can't see that ever happening. It will take years to undo the damage that has been done, the human cost has already been too great and will only get worse is the horrible truth.

It's not only the benefits system that has to change for this to work it's the very nature of employment and societies attitude to disabled people that has to change too, and that will take more than a year.   




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Condems, Bringing 19th Century Values to 21st Century Britain.

Captioned Photo Kindly provided by Christos Palmer

I was reading "A Christmas Carol" by Charles Dickens yesterday, a book written in 1843, and I'd like to share this excerpt from the first chapter.

Two men enter Scrooges office on Christmas eve asking for charity for the poor.

.... "at this festive season of the year Mr Scrooge," said the gentlemen, taking up a pen "it is more than usually desirable that we should make some light provision for the poor and destitute, who suffer greatly at the present time. Many thousands are in want of common comforts sir."

"Are there no prisons?" asked Scrooge.

"Plenty of prisons" said the gentlemen. Laying down the pen again.

"And the union work houses?" demanded Scrooge. "Are they still in operation?"

"They are still" returned the gentleman "I wish I could say they were not"

"The treadmill and the poor law are in full vigour then?" said Scrooge.

"Both very busy sir"

"Oh! I was  afraid from what you said at first, that something had occurred to stop them in their Useful course", said Scrooge "I'm very glad to hear it".

"Under the impression that they scarcely furnish Christian cheer of mind or body in the multitude" returned the gentlemen "  few of us are endeavouring to raise a fund to buy the poor some meat drink, and means of warmth. We choose this time, because of all others, when want is keenly felt, and abundance rejoices. What shall I put you down for?"

"Nothing!" Scrooge replied

"You wish to be anonymous?"

"I wish to be left alone" said Scrooge "since you ask me what I wish, gentlemen that is my answer. I don't make merry myself and I can't afford to make idle people merry. I help to support the establishments I have mentioned - they cost enough; and those who are badly off must go there."

"Many can't go there; and many would rather die"

"If they would rather die" said Scrooge "they had better do it, and decrease the surplus population. Besides - excuse me but I do not know that"

"But you might know it" observed the gentlemen.

"It is not my business" Scrooge returned "it is enough for a man to understand his own business, and not to intrude with other peoples. Mine occupies me constantly. Good afternoon gentlemen."

Seeing Clearly that it would be useless to pursue their point, the gentlemen withdrew. Scrooge resumed his labours with an improved opinion of himself, and an even more facitious temper than was usual with him...


As you can see the attitude towards the poor and destitute in Britain is becoming chillingly close to that of 19th century Britain. The current government is bringing values from that century that even the Victorians were ashamed of  and sought to bring to public attention the hypocrisy and barbarism of as early as 1843 to this century.

So before you harshly judge a benefit claimant as workshy or a scrounger remember, the welfare state was bought in to put a stop to the inhumane methods of dealing with the poor used before it's creation. The benefit claimants of today are no different to the poor and destitute of the Victorian era. Do not let the government drag us back to the 19th century with their propaganda about "benefit dependency" and "tough love".

The only thing that will end benefit dependency and help the long term unemployed and sick and disabled back to work is job creation, and a more sympathetic and helpful attitude towards them, that enables them to get work and remain employed. Labeling, hounding and cutting off benefits will not help anyone except the government in their endeavours to save money, caused by a crisis they created with their relentless pursuit of profit over humanity. 




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Atos Are The Number One Provder of Occupatuional Health Services In The UK.


Last night I was furious to discover that giant multinational IT company Atos is not only responsible for administering the government's hellish Work Capability Assessment, they have also been providing occupational health services in this country for years too, in 2010 they even won an award for it.

So they are declaring the sick capable of work, then if you are lucky enough to get a job (if your not one of more than half the people declared fit for work who end up destitute) you will still probably have to put up with them telling you how much time you can have off when your illness returns. As none of these people being declared fit for work have actually got better, they are just expected to work around their disability, so there is no escape from the bastards it seems.

Yesterday I learned that Co-Op uses their occupational health services, so much for ethics eh? They have posted a statement saying they can't just close the contract but will consider not renewing it. So DPAC are encouraging people to boycott them and go and inform them of this on their facebook page, at least until they issue a statement saying they definitely won't renew the contract.

I did some digging last night and found that:
 
And two county councils I found also use them

Since they are apparently the number one provider of Occupational health services in the UK there must be many more companies and councils using them too, and I saw lots of job vacancies for them posted all over the country.

This post informs you of much money they are raking in with double digit growth in the UK this year, as lives are daily ruined and even ended by the software they own the copyright to. And I'm also learning that this huge multinational company owns oil companies (including Shell and Esso), electronics manufacturers and many more highly profitable companies, more on that to come as I collect the evidence.




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Guest Post By Lynn AKA "Sign And Save Lives"

Guest post by Lynn

My name is Lynn, I’m 60 years old and I’d like to share my son’s illness with you all to try and help you understand the predicament thousands of others like my son are faced with next year, regarding DWP Benefit Reform for the sick and disabled.

My youngest son aged 40 has suffered from Paranoid Schizophrenia and emotional instability Personality Disorder since the age of 18. I have lived the illness with my son, the highs, the lows, and numerous hospital admissions over the years. My son had another very bad psychotic breakdown in August 2010, which resulted in a section 3 of the Mental Health Act and he has been in hospital care for 2 years this time.

Although my son is nearly 40 years old, mentally he is only 15, he is immature and extremely vulnerable and easily exploited. Therefore needs much support and care when living in the community.

My son, like thousands like him, who suffer from a Severe and Enduring mental health problem, has no voice when it comes to the DWP or ATOS, he like others wouldn’t be able cope with being interviewed next year 2013 when the Disability Living Allowance changes to Personal Independence Payment and he has to be assessed by DWP.  He, again like many others, who suffer severe mental illness, doesn’t believe he is ill, and just wants to be left alone.

The severely mentally ill will be hugely disadvantaged by the GOV/DWP/ATOS putting them through this ridiculous assessment in 2013, particularly people who don’t believe they are mentally ill, who to anyone who doesn’t know them, or, their background, can come across as fine, strong, healthy people, and may not appear ill at all, or, that they need help and support in their day to day lives, keeping them and others safe in the community, they won’t see the risks for the mentally ill, and many won’t have family or support to go with them to the assessments!

My son would tell an assessor he wasn’t ill, and say he just wanted to be left alone to get on with his life, which would see him losing his DLA/PIP for sure. Yet in reality, my son cannot get on a bus or use any public transport due to his paranoia that people are staring at him. He would get upset and get angry, probably end up getting in to trouble, because his self-esteem is low as is his confidence, and he thinks the world and his mate are against him.

To avoid this kind of stress and a way of coping, he needs taxis to anywhere he has to go, shopping, to any appointments he has. It is the only way he can cope with going out, and without his DLA/PIP he would be housebound and have no quality of life at what so ever.

If mental health sufferers lose their DLA/PIP benefit, (same as all disabled), it will place a huge extra burden on family, carers and friends emotionally and financially to provide the care and support and finance they need, which most of us couldn’t afford! All to often family/friends who are carers, as in our own case, are ill, worn down.

I was diagnosed 2 years ago with Moderate to Severe ME/CFS and told by my consultant it was due to being a carer for 22 years. My husband is 76 years old, in bad health, tired, it catches up with us and having to provide even more care to our loved ones should they lose their benefit, will put carers at more risk mentally and physically.

Because I understand the plight of the severely mentally ill, and have insight to the wider implications of what the GOV/DWP actions will cause for the sufferer and family, and carers, I have started this e-petition asking the Government to Exclude all severely mental ill from the 2013 DLA/PIP assessments, because what the GOV/DWP are doing is the biggest travesty and betrayal to our sick and disabled who in most cases have already proved their illness/disability with medical evidence and assessments they have already had to go through to get their DLA in the first place, and many like my son, were awarded DLA for an Indefinite period because they have provided proof their illness/disability is a life long one!

There are a number of e-petitions about Benefit Reform, I have signed them all which everyone should do to try and help protect all disabled, however, this petition is specifically to try and get the severely mentally ill EXCLUDED from the assessments because they do not have a strong enough voice and they will be hugely disadvantaged as I said before.

As a mum of a severely mentally ill son, and on behalf of all other sufferers like him, I know these assessments will cause SUICIDES in our most vulnerable, and cause huge hardship all round, please may I respectfully appeal to your good hearts and souls to support this e-petition and sign it, to share it with family & friends, on twitter/face book accounts, groups you may belong to, as I need 100,000 signatures to stand any chance of getting the House Of Commons to debate this, and at the moment I only have 2,456 signatures,  we only have until March to get the 100K!

Thank you all for taking the time to read this my plea, and I very much hope you will feel able to sign this petition.
http://epetitions.direct.gov.uk/petitions/35092

Kind Regards

Lynn
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You can follow Lynn on Twitter  > @SignSaveLives




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High Court rules Work Capability Assessment arguably unlawful

This is a press release from earlier this year about the judicial review that is due to be heard at the Royal Courts Of Justice on the 15th, 16th and 18th of January 2013. Lets pray it goes in our favour as it will open the floodgates for legal action over the WCA if it does. 

Thursday, July 26, 2012

The High Court has today granted permission to two disabled people to bring a claim for
judicial review against the Secretary of State for Work and Pensions to challenge the
operation of the Work Capability Assessment (WCA).
WCAs are face to face interviews carried out by healthcare professionals (HCPs)
employed by Atos Healthcare (a private contractor), to assess disabled people’s
entitlement to Employment and Support Allowance (a sickness benefit that has replaced
the old Incapacity Benefit). Each existing recipient of Incapacity Benefit is now being
assessed for eligibility for ESA, at the rate of some 11,000 people per week. WCAs have
been the subject of serious criticism by all relevant stakeholders in civil society including
doctors and NGOs working on behalf of disabled people.
The present case concerns some of the problems with the system as experienced by
people with mental health problems. Although medically trained, Atos HCPs typically
have very limited knowledge of mental health. The interviews are often hurried, and rely
on applicants to explain the limitations on their ability to work.
This is a serious problem for people with mental health conditions who lack insight into
their conditions, whose conditions fluctuate in seriousness, or who cannot easily talk
about their disability. Such people are placed at a substantial disadvantage in navigating
the system. Even if they appreciate the need to get expert medical evidence for
themselves, they are often less able to navigate the system successfully and to obtain
the medical report that they need. The Equality Act 2010 requires the DWP to make
reasonable adjustments to avoid such disadvantage.
The reasonable adjustment to the process that the claimants seek is for medical
evidence to be sought by the Atos HCP and the DWP at the very outset of the claim.
This would ensure that very sick people for whom having to go through a WCA would be
extremely distressing are exempted from the process, and for those that do attend a
WCA, the assessment of fitness to work takes place in the correct medical context, so
that dangers associated with forcing people back to work are correctly identified.
At present, the DWP do not routinely ask for expert medical report from an applicant’s
community-based doctor. The judge has held that it is arguable that this failure is a
breach of the duty to make reasonable adjustments, and is therefore unlawful.
In granting permission to apply for judicial review, the judge stated:
“I consider that it is reasonably arguable that the reasonable adjustments
required by the [Equality Act 2010] include the early obtaining of independent
medical evidence where the documents submitted with the claim show that the
claimant suffers from mental health problems and that this has not been done, or
at least not done on a sufficiently widespread basis”.
The claimants, known as MM and DM, were granted anonymity by the court. Their
solicitor, Ravi Low-Beer of the Public Law Project said:
“The present system results in many thousands of unnecessary appeals at great
public expense, with a high success rate. What is not counted is the cost in
human misery for those people who should never have had to go through the
appeals process in the first place. This could be avoided if doctors were involved
in the assessments at the outset. The Government’s policy of by-passing doctors
is inefficient, unfair, and inhumane. We gain heart from the court’s finding that as
a matter of law, it is arguable that something has to change.”
For further information contact Ravi Low-Beer on
r.lowbeer@publiclawproject.org.uk/0845 543 5944
or Adrian Lukes on
a.lukes@publiclawproject.org.uk/0845 543 5946.
Public Law Project (PLP)
PLP is an independent, national legal charity which aims to improve access to justice for
those whose access is restricted by poverty, discrimination or other similar barriers. To
fulfil its objectives PLP undertakes research, policy initiatives, casework and training
across the range of public law remedies.
For more information on our work, events and publications: www.publiclawproject.org.uk




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Paint Your Red Nose Black In Protest 2013


This year I and others are painting our red noses black and intend to boycott the television shows we'd like you to join us, and I'm sure you'd like to know why? We are not against Comic Relief or the good work it does and encourage you to buy a red nose if you can afford it. But this year Comic Relief saw fit to include clips of David Cameron in the music video to One directions charity song. We feel including the Prime minister in this video is a slap in the face to the millions of people he has plunged into poverty in this country with his misguided austerity measures.
There are currently 3.6 million children in the UK living in poverty according to barnardos 58% of them are in a family where someone works.
Yet the Coalition have pushed through measures to ensure benefits even those for disabled people and people in work, like tax credits only go up by 1%. Further punishing children who will be forced further into poverty as their parents incomes are reduced even more compared to inflation.
These cuts risk putting the UK in breach of the UN Economic and social rights convention we are signed up to. Food poverty has risen so sharply that there has been a massive rise in emergency food banks already.
The cuts to housing benefit for many people living in social housing deemed to be over occupying their properties dubbed “The Bedroom Tax” Will see people expected to move to a smaller property or pay a charge for their extra room, even though there is a huge shortage of suitable smaller properties for them to move to. This will further increase the poverty people are suffering in the UK as they are forced to make up shortfalls in their rent or face eviction and homelessness.
The coalition also rolled out across the country a new and untested Work Capability Assessment when they came into power in 2010. Between January and November 2011 10,600 disabled people who clearly wrongly had their benefits stopped died within 6 weeks of losing benefit. (a sharp rise in the statistics compared to the year before).
Yet despite all these alarming statistics David Cameron's ministers continue to claim these cuts are fair and needed. Though they have made no cuts to their own wages, continue to claim massive expenses, and have not sufficiently cracked down on tax evasion by large multinational companies. But apparently we are “all in this together”.
We presented all this information to comic relief and they have ignored our requests to remove David Cameron from the video, and have even promoted pictures of David Cameron's wife Samantha baking in her tax payer funded kitchen at Number 10 with her children. Making cakes she will apparently sell to downing street staff to raise money for the event. Well it's alright for some isn't it?
Join us by liking the facebook page where there is a list of actions you can take and by tweeting your disgust at this flawed decision by comic relief using the hashtag #blacknoseday.




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Atos monlogues "Internet Survey number 2" for art action week project.

Picture by Stewart
If we're going to do any of the Atos monologues I'm going to need a lot of volunteers who can record themselves and somehow send the video, because of the amount of time we have I think we can only do a small part. Mainly because we don't have time to send larger videos which would probably have to be sent by post on a disc. There are a lot of lines in this part, and the resulting videos will hopefully be short enough to email or send over facebook. If you just upload them to the art action group I can download them from there.
I've moved this post onto the blog as it's easier to share a link to it, and I can strike through the lines that are already taken.  If you want to take part chose the line you want to read from the list below, record it and you can send it to me through facebook. If you don't use facebook leave a comment and we'll find another way for you to send me the video. And if the line you wanted has a line through it sorry someone has already taken that one.
Here is the full Atos Monologues 2 script: 

http://www.scribd.com/doc/105841602/The-Atos-Monologues2
The part we are doing is on page 13
 

We can't see Post traumatic stress disorder and we've never heard of a hippocampus.
You do not meet my limited definition of being disabled
You drive an Audi. How would you afford it? It would be too difficult for a disabled person to get in.
You can text a friend
You can tweet
You watch TV and soaps and can sit comfortably for half an hour.  
I saw you stand up!
'You're too young'
You can pick up a £1 coin
"You seem alright to me"
"You're smiling"
You look butch. Can't be anything wrong with you.
You could fill in the form.
You brushed your hair this morning and you’re wearing a nice coat
You answered questions that was asked
You traveled by bus
You don’t soil yourself every day.
You could fill in the form
You’re still breathing
You can spell your name backwards
You're not a dribbling, disheveled lunatic howling at the moon and threatening to axe people to death
You hold eye contact
You don’t look disabled enough to me
You brushed your teeth this morning.
You’re faking it.
You can’t have Post traumatic stress disorder because "you've never been in a war zone"
You’re at university.
You have a girl friend.
You don’t look autistic
You can talk
I cannot see anything wrong with you
You moved your leg.
You can lift an empty box up to waist height.
You’re so pretty.
PAUSE
You can’t be disabled because of Tory ideology




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List Of Brands Available In The UK That Use Monsanto Products.

   
Complete list of UK Brands that use Monsanto products, so these companies products probably contain Genetically Modified ingredients. Boycott all these companies for the good of your health!  This site is very useful too called "How To Avoid GM Foods". And also check out "GM Watch"
And if you are in the USA watch the video at the bottom of the post for a full list of products you should be boycotting too.
Betty Crocker
Cadbury
Campbells
Capri Sun
Carnation
Coca Cola
Quakers
Green Giant
Heinz
Hellmanns
Nestle
Spam
Kellogs
Knorr
Kraft
Lipton
Minute Maid
Ritz Crackers
Ocean Spray
Pepsi
Pilsbury
Power Bar
Pringles
Proctor and gamble
Quaker
Ragu
Weight Watchers
Schweppes
Uncle Bens
Unilever




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More Propaganda Broadcast "Don't Worry Disabled People Are Fine, Go Back To Sleep..."

Just been listening to BBC Radio Four, they were discussing disability and finances and how disabled people have more of a hard time getting loans. they also went into how it costs more day to day if you are disabled, how this is worse in the current economic climate, and mentioned welfare reform and bedroom tax, giving an example of one woman who has to now pay £20 a week she can ill afford. The report quite good and balanced up until that point, then they read out the government response.
They said that they are "Committed to helping disabled people" still spend 58 billion on disabled people, and that a number of disabled adults and children are actually getting more money under welfare reforms. Then went on to say something about some scheme to help disabled people say no to dodgy loans and expanding credit unions.
I couldn't believe it, I only know one disabled person who is in fact getting more money as a result of welfare reforms. I know many people who have lost money and are afraid they will lose more money when PIP comes in. Nearly every one of my friends who has mental illness has lost ESA on appeal, including myself, the mentally ill are always the first to be screwed over when there are cuts after all.
They completely ignored all the negative impact their reforms have had in their response and as usual didn't apologise one bit or admit welfare reform had gone wrong, it was a disaster, and they were sorry, let alone tell us they were working on putting it right.  They just gave this reassuring response that practically said "go back to sleep, disabled people are fine..." even though the show had just given an example of a person who was suffering.
And to add insult injury those of us who campaign to raise awareness of what is actually happening are now labelled extremists. I just hope the general public aren't falling for all this rubbish, though lets face it they probably are...




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I've moved the blog!

You can find all my old articles and new posts here

http://nancyscrazyadventures.wordpress.com/

Goodbye google




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Ijsgang verhinderd uitvaren reddingsboot Ameland

Door de ijsgang kan de reddingsboot, van het planerende type, van Ameland niet uitvaren







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Le roi d’Arabie saoudite gracie la jeune femme condamnée après un viol

La jeune femme avait été condamnée à six mois de prison et 200 coups de fouet après avoir été victime d’un viol collectif. Le roi Abdallah d’Arabie saoudite a accordé sa grâce à une jeune femme qui avait été condamnée à six mois de prison et 200 coups...




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Bolufer et son pied-à-terre

Le directeur de cabinet de Christine Boutin, actuelle ministre du Logement, loue depuis 1981 un appartement à loyer modéré propriété de la RIVP (la régie immobilière de la ville de Paris). Selon le Canard enchaîné, qui révèle l’information, Jean-Paul...




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Le ''droit au logement opposable'', cette fausse bonne idée, par Jérôme Dubus

Depuis une décennie, hiver après hiver, l'histoire bégaye : la France fait mine de découvrir la grave crise du logement à laquelle elle est confrontée. « SDF » qui nous renvoient le miroir de nos propres insuffisances ; « mal-logés » qui se réfugient...