Four weeks later he is diagnosed with bacterial meningitis, leaving him with severe epilepsy and cerebral palsy. Doctors at the hospital tell you that he will never be able to see properly, talk, walk or even crawl. Your son then begins to have random and scary, hour and a half long seizures at all times of the day and you are making trips to the hospital almost daily. There is nothing the doctors can do but to wait. All medications prescribed by the hospital staff either had minor or no effect on his condition. The only thing that will help your son would be Cannibas oil. What would you do in this situation? Would you be willing to break the law to save your son? This is the question Cassie Batten and Rhett Wallace continuously ask themselves. This situation is their day-to-day life with their son Cooper. Cassie gives her son a small dose of Cannibas oil mixed with his milk almost four times daily and the results were almost instantaneous, after 15 minutes they started seeing a massive improvement. During a broadcast on …show more content…
Thus, it is not wrong on those grounds. Yet, shouldn’t something be said about the autonomy of the client. We must recall that, when mishandled, marijuana can prompt addiction, some psychological/cognitive harm and memory loss. Those outcomes would fairly affect the autonomy of a client. In this way, there are some Kantian reasons against it. Similarly, abusing alcohol, or eating an excess of sugar or cheeseburgers might genuinely compel someone’s autonomy. Along these lines, we would have Kantian reasons against misusing those things. This is not to say that the same reasons apply to utilising them. We ought to be likewise worries about around a likelihood that an individual misuses marijuana, maybe develops an addiction and starts doing hurtful things to themselves and
Hy5 is known as the industry's leader in flood damage repair in Ulverston, using top ranking techniques and flood specialists who are well trained in operating modern equipment and effective cleaning products.
Many people could be affected if staff did not ffollow regulations, an outbreak of food poisoning could occur and this would affect the service, people we support, staff and visitors and they could become very ill with diagnoses of sickness, diarrhea, which could lead to being admitted to hospital and have further complications as well as be less able to fight off infections, or be vulnerable due to their age/lifestyle/circumstances. This could also affect people in an emotional way. For example stress and worry. Some staff may want to stay off work as they would be worried they will catch an illness and this would affect the service staffing levels. Family and friends would be angry, worried and may not be able to visit. Reputation of the
I will now talk about each patient needs as they all differ from each other. Nusrat Patel is 19 years old and has learning disability. This means Nusrat has difficulties in keeping knowledge and skills to the expected level of those the same age as her. Nusrat also has epilepsy which is neurological brain disorder when someone has epilepsy, it means they tend to have epileptic seizures, a seizure is a sudden attack of illness. Nusrat has left residential school to receive full time carer from her mum who has stopped working to care for Nusrat. At times this can be stressful so Nusrat attends the community centre on Tuesday and Thursday which allows Nusrat mother to have a break. Maria montanelli is 34 years primary school teacher who is much like Nusrat mother and takes care of her 96 years old mother who has dementia. Dementia is memory loss and difficulties with cognitive development. Being a primary care for her mother Maria feels she not performing at her best ability because of her lack of sleep which occurs when she assists her mother to the toilet several times. The last patient I would like to mention is Alice Fernandez she is 74 years old who recently lost her husband who had lung cancer. Alice doesn't use her pension the right way as she purchases many drinks as an alcoholic and has increased since her husband passed away. She has been prescribed antidepressant tablet by her G.P but made her lethargic this means she's become slow and sluggish.
For this assignment, I interviewed a parent of a child who does not have an IEP or receive special education services. Through this interview I was able to learn how parents of children with no special needs are aware of the inclusion classrooms.
The patient is a transgender and has HIV. Our society has not fully accepted transgender as a societal norm, because of their gender identity and expressions are different to societal expectations of gender. The patient hardly has family support, which can possibly cause poor adherence due to isolation. HIV
What happens if a member of staff phones in sick but they are later seen out at the shopping centre or down at the pub? Does that mean their skiving?
This problem question is about claiming for damages due to psychiatric harm. It involves questions regarding primary victims, secondary victims, and special duties problems.
Over the last century health and social care has changed and developed immensely with the implementation of the NHS and becoming a welfare state. Prior to this health care was only available to a minority of people, those who could afford it. In 1815 the old poor law was passed, it stated that each parish must look after its own poor and those who could not work were provided enough money to help them survive. By 1830 the poor law cost around £7 million, which came from taxing the middle and upper class, causing a sense of resentment towards lower class, unemployed people. In 1834 the new poor law was passed, its aim was to reduce the cost of looking after the poor. Workhouses helped with this, they provided clothes, food and healthcare in return for manual labour. Despite
On 4/21/17 at 0715 hrs, I was dispatched to 6154 110th Ave N, in reference to an emotional crisis. Upon my arrival, I made contact with the Charles Hollen, at the front door of the residence. Hollen advised he wants to go to the hospital to receive help.
There are many things which can affect access to complementary therapies. The ones I will be explaining are:
Reporting of Injuries,Diseases and dangerous occurrences regulations of 1995 requires the reporting of work-related accidents, diseases and dangerous occurrences. The Act applies to all work related activities, but not to all work related incidents. The objective of the regulations is to enable the enforcing authorities to identify where and how risks arise and to investigate serious accidents so as to prevent them from occurring in the future and thus providing a safer work environment. The enforcing authorities can then help and advise you on preventive action to reduce injury, ill health and accidental loss,the main points of our own policy that relate to this are:
No Secrets – Guidance published by the Department of Health, builds upon the governments respects for human rights and highlights the need to protect vulnerable adults through effective multi-agency work.
This is 31 year old white male. Patient is here with several complaints as listed. Patietn was seen at UAB ED yeaterday for the same conditions and discharged without any treatment; "They don't like me there, UAB, because I have a long history of drug use and frequent use of their ER." Patient denies chest pain, SOB, N/V/ D. Patient is a current tobacco user with 20 apck year hisotyr. No substance abuse for the past 3 months. Current pain
53 year old female complaining of pain underneath her R-breast close to the rib cage area. Pt described pain as being constant. She is unable to sleep has pain when she takes a deep breath, pt also complaining of dizziness.
Charlotte and her twin sister, Chase, were born on October 18, 2006. At first, everything was fantastic for the Figi family. Their lives took a drastic change three months later when Charlotte had her first seizure. This first seizure lasted about thirty minutes. Her parents rushed her to the hospital where her parents were told that every test they did came back normal. This happened a few more times, with each seizure getting worse. Finally they got an answer, however, it wasn’t a good one. Charlotte was diagnosed with Dravet Syndrome. As Charlotte got to about the age of 2, she was on several different medications for this horrible diagnosis. There is no cure for Dravet Syndrome. The Figi’s tried everything for their daughter from barbiturates and benzodiazepines to specialized diets for epileptic patients that didn’t respond to normal treatments. Running out of treatments and out of time, Charlotte’s father was scouring the internet while overseas with the military. He came across a story of a little boy with Dravet Syndrome being treated with cannabis oils. It worked for this child! Charlotte’s parents, who were very against marijuana use, didn’t know what else to try. By this time Charlotte had lost the ability to eat, walk, talk, and even really function. She had went into cardiac arrest several times. Her parents were so afraid of losing her, they were willing to try anything. After a lot of hardship trying to find a doctor willing to prescribe a five year old medical cannabis, they finally got the break they were looking for. The next hurdle to jump through was finding a dispensary that would sell her the much needed marijuana. Finally, Charlotte’s mother found two ounces of low THC- high CBD marijuana at a store, and bought all that she could. This cost her eight hundred dollars. She had a friend who knew how to extract the oils from the marijuana. She