Showing posts from 2012

Our miracle son, cancer, disability, SPD, Love and Family..

Help us someone... Some one please help me, as i am suffocating from the system we have in place, a system in which is breaking me as a person as i am already broken as a mother as my son has cancer, this is such an emotional suffocation of hurt for my son and the wish i could change places with him, the hope, our miracle that is our son, can survive and the maliciousness of humankind that has shown its ugly head at a time our family should be supported, not attacked, could be somehow hidden from our son, so we can protect him from it, but it is him that suffers with us. We should not be investigated or have a child protection conference for a child that is already protected by my husband and i, and his grandparents. I would DIE for my son, i would take a knife, a bullet, anything for my son to be able to live, even if for only a second longer than god has planned, because my son IS my life. He IS our life, and they are all asking us to forget it is happening, put it in the back

Focus on the Positives no matter what life throws at you!

We have moved home to a new property that meets my medical needs and we couldn't be happier here. Our son is blossoming into a little boy and he will be starting nursery next year! *shocked face here* Where! Oh Where! Did the years go? Feeling the same? I know how you feel! We are making new friends, old friends are moving on, and we are just following the path that life is leading us right now, it is not all sunshine and rainbows, we do have obstacles surpassed and more obstacles to conquer, but we prefer to focus on the positives and we find the negatives usually get sorted out when we're face to face with them. So it is nice to focus on the positives and be cheery and chirpy and looking forward to many years to come, growing old together as man and wife, watching our son grow up to be a man and filling our parents shoes when we reach their age and our son has a life of his own.  We all grow, we all move forward, and life is quite short despite it being th


Well, on a very much used Social Networking Site starting with 'face' and ending with 'book', we had yet another of our SPD AWARENESS DAYS! For those that are not aware: SPD AWARENESS DAY was set up by charity Support Pelvic Dysfunction and this blog, to be every FEBRUARY the 1st. (WHY THIS DAY? because that's the day we thought about this fantastic awareness idea that would help many SPD victims find us!) Every FEB 1st people on this networking site set their status to say something along the lines of: "Well it's another SPD awareness day started by Support Pelvic Dysfunction! Please REPOST this as 1 in 3 women develop SPD, approx 20% become disabled with SPD or develop long term SPD. Help is available at Let's raise some awareness today! HAPPY SPD AWARENESS DAY! ♥" Then people who WANT to help click SHARE and post it to their wall or set it as a status. This year it was also shared on anothe

RE: PREVIOUS post regarding disabled being non-equal citizens:

In response to the post i made previously in regards to how disabled people ARE NOT equal citizens unfortunately, i have taken action today and put my thoughts accross to my county council. ALL details and names have been removed to protect identities and to follow the rules of the blog that i established based on morals, but the opinions i have and how i have put them accross has been kept as i said it. Please read on and i will update you in regards to what reply i get, still following legal guidelines and protecting identities. REMEMBER: PLEASE SEE PREVIOUS BLOG POST AND SIGN THE E-PETITION TO NUMBER 10 DOWNING STREET TO CHANGE CARERS ALLOWANCE TO A HIGHER AND MORE DESERVING AMOUNT! TAKES NO TIME AT ALL TO SIGN IT! Complaint below: "HIGH PRIORITY: DISABILITY NEEDS COMPLAINT AND SUGGESTIONS PRIVATE AND CONFIDENTIAL To whom it may concern, I would like to put forward a formal complaint and suggestions regarding disabled tenants. At this moment in time, disabled