He lives with me and it’s been 5 months of so much loving, learning and living.
He lives with me and it’s been 5 months of so much loving, learning and living.
I have written extensively on mental health, mental wellbeing and mental illness on my own website, blog and the Gbm Foundation for epilepsy and mental wellbeing of which I am the Country Director; and on numerous national and international media. But, these serious foursome Ss pop up again and again – seems like there will be no meaningful progress until they are squarely addressed.
S1: SPIRITUAL ATTACK
When you are in a very religious country or community, you should realize that religion and spirituality or whichever comes first to the people, plays a very big role in their lives. Indeed, long before ‘white man’ medicine came, people were cured or healed through incantations and other process including drinking various portions and following special protocols. A spiritual attack is when there is a belief that the origin of the attack is mysterious especial when no other logical explanation exists. Truth be told, no logical explanation exists to explain a mental health challenge or disorder, and the first stop when there is a crisis here, is mostly to a Man or Woman of God. Hold up, they are actually competing or on the same line of importance as the traditional doctors when we consider the second S.
Even where it can be ascertained it is a spiritual attack, the source must be rooted out right? Who else but a jealous person or witch/wizard can cause someone to have a mental health problem or illness? The predominant belief in our communities had always been that any sudden illness or death is superstitious and very suspicious. Mental health challenges or illnesses are no exception. Indeed, for these categories of ‘wahala’ (local slang for trouble), it is the norm and can only be cast out or cleansed by the traditional doctor aka Ngambe man (witch doctor) for us. I mean, if neither the spiritual healer nor the herbal healer cannot help, why not just chain up the person and let them waste away and die instead of bringing more embarrassment to all concerned? The next S comes in here.
Stigma is both from without and within. The society and even families stigmatize the patient and their family; and the patient loses all their self-esteem and stigmatize themselves by withdrawing further and further into their own ‘world’. Families get fed up trying to help while navigating all that stigma, and the patient’s ‘supposedly non-compliant attitude’ only makes matters worst. Tie them and lock them up or outside in a barn let them become whatever they want. The patients equally fed up with the treatment and stigma, lookout for ways to live their ‘freedom’ and to ‘communicate their frustration’ in anyway that appeals to their already very distorted cognition. Society notices and sighs in slushed sentences and all stakeholders are at a lost on what to and how to proceed. And then the next S.
Note I write the last two Ss in all caps. My own way of shaming them actually. Shame can make even families with the means to take their patients to the hospital and seek better and alternative treatment protocols not to do so. Shame is the outcome of all the stigma explicit or implied, and we all know how people could sometimes fight to protect their ‘reputation’. We have surely heard of ‘honour killings’ in some countries where families have taken the lives of one of theirs because of the shame this individual was bringing to their name. Some patients out of shame, could also contemplate or commit suicide because the life they now lead is definitely the skeleton what was before they fell ill and they can’t stand the pain, stigma and all any more.
It is therefore my humble submission that we in Cameroon have to address these foursome Ss if we are to really make any progress with any mental health campaign. Our realities are still far different from those of the west, I saw this first hand when I did a two months internship at the lone public psychiatric ward in the city of Douala. Many patients brought in are already so challenged and ill, it’ll take much more than a brief hospitalization to help them. Some even in the hospital don’t open up to get any little help available, they are ashamed or feel stigmatized even by some medical personnel – sad to admit.
Today as we celebrate World Mental Health Day under the impressive theme Young People and Mental Health in a Changing World, I salute the efforts made to raise awareness to the different issues involved surrounding mental health, but I add that we should step up our listening. Sometimes people hurt so bad but there is just no one to listen to you even when you want to trust enough to tell.
Marie Abanga is a phenomenal woman by every account who defines herself simply as a person of passion and a tale of talents. She runs a private psychotherapy practice in the city of Douala – Cameroon and be contacted through her website at https://marieabanga.com.
Engaging in addiction recovery may be the most important challenge you ever undertake. It’s vital to use the best tools available to you. Alternative methods can help you achieve success.
Holistic therapy. There is an increasing awareness of holistic therapies, with some studies showing sixty-five to eighty percent of the population participating in holistic naturopathic medicine as a primary form of health care. Demand is so great, half of all medical schools offer courses in holistic methods. Holistic therapy is defined as treating the mind, body and soul of a person, and typically uses both traditional and alternative methods to address and prevent health conditions. Practitioners aim to treat not only symptoms but causes of issues, they encourage communication with patients, integrate whole-body approaches in their programs, and support not only physical concerns but also mental and spiritual ones throughout treatment.
Some of the alternative methods used in holistic-oriented addiction recovery are as follows:
Acupuncture. Acupuncture is a time-tested therapy using needles to reduce cravings, aching muscles, detoxification symptoms and withdrawal symptoms. According to HealthLine acupuncture works to help to restore the body’s balance.
Biochemical restoration. This treatment examines what imbalances in the body are producing cravings and restores balance through nutrition.
Biofeedback. As The Treehouse explains, with biofeedback, machines monitor brain waves to evaluate what is occurring during an addict’s cravings. By understanding the addict’s thought patterns treatment can be modified to address issues.
Exercise. Some experts note exercise helps improve mood, enhance brain function, and improves strength, flexibility and cardiovascular health. Addicts can enjoy achieving a natural, healthy “high” through the chemicals released in the body by exercise.
Herbs. Symptoms of detoxification can be treated with herbs like valerian, kaya, and ginseng. Some herbs reduce insomnia and anxiety as well.
Hypnosis. By instructing the subconscious mind toward different thought patterns, an addict’s self-esteem can improve and the desire for drugs be eliminated.
NAD. Nicotinamide adenine dinucleotide (NAD) is a derivative of vitamin B3 – also known as niacin. It’s a basic element in all living cells and plays a key role in metabolism. NAD is thought to help reduce cravings and withdrawal symptoms during recovery.
Prayer and meditation. These two therapies are similar, requiring the addict to focus intently and embrace a higher level of understanding.
Yoga. Yoga encourages engaging mind, body and spirit to improve patience and relaxation. Addicts learn to look inward to understand their choices and navigate recovery.
Holistic treatments should be used in conjunction with rehabilitation and lifestyle changes. You should embrace a healthy diet and fitness program, and understand emotional wellness is a key component in recovery. Psychotherapy, mental health and behavioral therapies can help improve emotional health.
Exercises such as journaling benefit many addicts. Journaling provides the opportunity to review patterns and look inward for what drives your personal choices. It also encourages you to stay balanced and maintain a healthier focus on reality and on the present, reducing anxiety and stress.
What alternative methods aren’t. As explained by Psychology Today, alternative methods are not meant to be stand alone treatments. It’s important to participate in an organized recovery program guided by proven treatment practices. Ensure your care provider is using evidence-based therapies and treating your whole person with other proven methods. As some experts explain, everyone is different and your program should be tailored to your needs. Any treatments should be discussed with your therapist and used in conjunction with your entire recovery plan. Engaging in a treatment on your own, especially if it neglects another vital component, can be dangerous. Ensure you participate in a healthy, balanced recovery plan with the guidance of your therapist.
Alternative therapies can help. Addiction recovery is a difficult road, and with alternative therapies you can better navigate the obstacles. Discuss your options with your health professional. With a sound, balanced approach your recovery can be a success!
About the Author
Kimberly Hayes enjoys writing about health and wellness and created PublicHealthAlert.info to help keep the public informed about the latest developments in popular health issues and concerns. In addition to studying to become a crisis intervention counselor, Kimberly is hard at work on her new book, which discusses the ins and outs of alternative addiction treatments.
P.S: I am sincerely very honoured that Kimberly sent me a request to do a guest article on a topic I was embracing after coming in touch with the terrifying reality on the ground. When I did my internship at the lone psychiatric ward in my city of Douala – Cameroun, about 2/3 of the teenagers admitted were for addiction and dis-intoxication. I definitely can’t wait for her book’s release and hope she writes another article for my blog.
Hello World, very honoured to be wrapping up my interviews with authors who have written on mental health, with one I fondly call Granny. I was so delighted to talk with her on phone when I visited the US in 2015, and I was so happy when she liked the memoir I mailed her.
I have done a modest review of Jill’s heart breaking memoir on my blog, and it is my honour to interview her too. I don’t know how a mother handles her only son’s mental illness and survive his loss, I see my mum dwindling between striving and surviving but I am not in her mind. I hope Jill tells us a little how because she is one of those brave mothers!
1) The Profile
Let’s Start with a brief introduction of yourself – your background – and a tiny bit from your life before mental illness struck:
I was born in Bloemfontein, South Africa in 1939 and had an enchanted childhood. I studied teaching in Cape Town where I met and fell madly in love with Alec. We married, and immediately, our relationship was a loving and caring one consisting of give and take. After our baby, Doron was born, we left family and friends to fly off to Israel, the country of our dreams.
(Doron means ‘a gift’ in Hebrew.) The real name of her Son refered to in the memoir as David
About your Memoir, why did you write it all those years later and with many names changed as you say?
Because I had never written before. But, I wrote notes every night on what had occurred each day from the time that Doron became ill which was during his arbitrary military service although in retrospect, there had been some signs previously. It took time but the book called ‘Weep for Them’ was born and published – the hardcover edition in 1998 and the paperback in the same year under my pen-name Sarah Ben-Dor. Neither were translated into English as I simply could not face rehashing that excruciating experience all over again.
Years later, after we’d lost our son, I had so much more to add, that I consulted with my husband and two daughters and asked for their permission to write an updated book in English, using my real name this time. They agreed. But I had to change the children’s names as well as my husband’s while writing because that made the whole process a little less painful for me as I was reliving the 16 years of Doron’s illness all over again.
2) The Soul Journey
What is your take about mental health?
When our Doron was diagnosed with paranoid schizophrenia, I had heard little about the subject and had never met a mentally ill person. Today, I am older, wiser, read whatever I can on new developments but, to date, am not convinced that there is something that could have helped our son who proved to be medication-resistant for so many years. I pray that somewhere, someone will be able to help all those who might be suffering the way Doron did. I never felt guilty about causing his illness as I had read that parents cannot cause schizophrenia.
Did your feel guilty for your son’s deteriorating mental health? If yes what did you think or do, if no please explain some to us.
A few older psychiatrists pointed the finger of blame at me, but fortunately, I had read enough to know that I was innocent of that, at least. I had to do something so, I approached the Israel Mental Health Association ENOSH, and asked for permission to start a support group for parents of mentally ill children in our neighborhood, in English, as Hebrew is not our mother-tongue. They let us use their facilities and offered assistance but frankly, most of us, 22 in all, did not want to hear another professional at that stage. We met regularly twice a month and became like one large family. We could speak openly about anything to do with our ill child, confident that we could trust one another to be honest and not to speak to anyone else about what was said. I felt safe with them, so much so that they became like an extended family.
Parents cannot cause schizophrenia.
Mothers cannot cause schizophrenia. I want every single parent to know this:-
I bet you all part 2 tomorrow is equally soul searching, captivating and near gut wrenching – stay tuned
What is NORMAL Anway?
This was the question I was ‘foolishly’ or maybe ‘highly unrealistically’ expecting to be answered in this all too human and yet piercing memoir.
I began reading this memoir by carefully studying the cover picture. I concluded the two chubby innocent girls on the front cover were Martha Graham-Waldon (MGW) to the left and her dearest sister Kathy Graham (KG) to the right. While MGW looked at the camera, KG looked more closely into the gaze of the pet birds they carried. I noticed her shirt lifted up a little and showed her tummy and yet that wasn’t a problem for the photographer. Yet, some of you may agree with me that in some cultures, keeping birds for pets, or not being properly tucked up be you kids, is simply not NORMAL.
This memoir did more to me than just help me see how another family just like mine had, faced and dealt with their member’s mental illness. MGW may not know to what extent her memoir will impact some, but it has definitely completely shattered this paradigm of ‘NORMAL’ to me.
Was NORMAL to be the absence of a diagnosis mindful of some signs that something was seemingly going on with KG? Was it now their new NORMAL that something was indeed going on with KG but then they had to ’embrace’ that as is, or ‘pretend’ to still fit in with ‘conventional community’? What about it being NORMAL to sympathize with their mum who suffered a stroke, and yet shy away and stigmatize the Grahams for having a ‘mad member’ in their family?
I am not going on any further, I read this memoir with so much attention to everything because I couldn’t really believe another family, far away in the USA, could go through such shattering trauma and deal with stigma too! I really thought such things happened only in Africa, to families like mine, well in a setting where people died more from ignorance than from Negligence. I don’t know what to make of the ‘medication tradition or pattern out there’. What is NORMAL now? Go after the symptoms? Go after the illness as diagnosed? Go after the person and beat the Shit out of them?
And in the process of it, how do you a close sibling deal and heal with it all? I applaud MGW’s vivid narration of their various exotic and adventurous family vacations and existence before ‘Life happened’. This in my firm opinion as an aggrieved sibling like herself, states the strong case that the ‘lunatic’ the world now sees, had a ‘NORMAL’ life before their mental illness. I am glad and actually obliged to MGW for writing this memoir mindful of her pain. I rate the book a 5/5 because of the ‘intensity of the different subjects covered’. If I could recommend only 3 books for your year end, this will definitely be one of them. If you read carefully and in between, you’ll definitely re-evaluate that word NORMAL.
About the Author
Martha Graham-Waldon is a writer, spiritual entrepreneur and armchair activist who resides in the Santa Cruz Mountains of California with her family and a menagerie of pets. Her articles have been published locally, internationally and online. She is a winner of the 2015 Women’s Memoirs contest for a vignette based on her memoir Nothing Like Normal: Surviving a Sibling’s Schizophrenia published by Black Opal Books. A member of the National Association of Memoir Writers, Martha also loves travel, the outdoors, Jazzercise and music.
Hello world, pursuant to P1, here is P2:
…This is actually the setting into which Precious, Victor and Mercy are born to papa Thomas and mami Maria. Papa Thomas is a doubting Christian who has fallen out with the church because he insists on wanting to take a second wife since mami Maria has so far giving him only one child (He refuses to count the first two sick children as his). He has surnamed this third child Mercy and although she is only a girl meaning of not so much value to him, he desperately needs the ancestors or God to have mercy on her and spare her from the ‘badluck’ of her siblings.
The movie takes us through the traumatic ordeal of Precious and Victor, an ordeal which begins at home and ends up in school. They are at first taken by their parents to the traditional healer where they undergo near fatal and highly superstitious practices in a bid to rid them of the ‘curse’ source of the badluck, and when the procedure fails, they are dragged to the church with the hope that the reverend father will exorcise the demons in them.
The movie also brings out the guilt, burden and pain mothers feel and bear throughout such ordeals. In our case, mami Maria the mother of the sick children, bears it all bravely, leaving no stone unturned to get her husband to change his staunch traditional mentality and try out the ‘whiteman’s medication’ for once. It is she who when at her stall sees the NGO’s sensitization posters, pleads desperately with her husband that they go to the mission hospital and attend their presentation to learn some more. She equally plead with the catechist to come talk to her husband mindful of his disapproval of papa Thomas’s penchant for polygamy. The catechist’s visit leads to their being received by the reverend Priest. Reverend Fada as he is calls, seizes the opportunity to dismiss all what has been said at the village square and the traditional healer as false beliefs/practices; nothing more.
The lives of Precious and Victor henceforth take a dramatic turn for the better once reverend Fada refers them to the mission hospital. He knows that help can be found at a hospital because his cook’s child who suffers from what he refers to as epilepsy, gets a lot of help from the hospital in the nearby village.
Precious is almost denied a chance at the ‘whiteman medication’ when her father papa Thomas grumbles that he doesn’t have money to take two children there. He will rather take the boy and leave the girl to end up which ever way. Her dear mother steps in again by bringing out her savings. There is no way mami Maria can let her husband blatantly and viciously discriminate against her two sick children because one is a girl and to him of little value, while the boy a younger sibling deserves all the chances at getting better.
At the hospital, the children are registered for consultation by the neurologist who comes during the medical missions organized by the NGO. This NGO which has been working on the field for barely two years now, has indeed been able to secure the personal support of one of the few neurologists in the region. The Neurologist they are told brings a special machine to test the brains of the selected patients so as to know the exact type of the brain disorder they suffer from, and to be able to prescribe medication which can prevent the fainting or seizures as the attacks are called in the hospital. The God sent NGO has also brought some subsidized medication which thanks to mami Maria’s savings, the family can afford.
All is well that ends well, at last the children can now go to school. Another exciting news is that they don’t have to fear the reaction of their teachers and fellow students if they have a seizure in school because the NGO has also brought handbooks about epilepsy for the teachers. The teachers will be trained and they will in turn teach the students on what to do if a friend is having a seizure. The NGO is even sponsoring the Fon’s Football Cup tournament (among other projects), so that through the sponsorship they can sensitize the entire community on the brain disorder and advocate for a change in mentality towards persons living with epilepsy – thus fighting against stigma. Epilepsy they emphasize is not contagious and so people will stop running away and shaming them when they are having a seizure. Epilepsy they even add can be cured and prevented. All this is so new, it makes the news in the whole village.
In the end, Precious and Victor become heros in their village. Their story is reported in the local newspaper and the NGO tells them they will be taken to the city to share their story. Soon, many other parents stop hiding their sick children at home, they take them to the hospital and write down their names so that they will be selected and called back when the NGO organizes another medical mission….
Stay nearby for P 3 next week and thanks for all the support
Wow, wow, wow – barely 3 days and my brother’s name is high over there on the banner for all to see. No he didn’t die in vain. No my pain was not in vain. And oh yes the gain is worth the lane no matter how winding.
Those banners worth thousands of messages
We at the Gbm-em Foundation have done all in our might and conscious of our plight, to get ready. We are going to walk with our sympathizers purple high.
On Friday already, there will be a one hour program over the CRTV radio, about this maiden and first of its kind solidarity walk for an illness still ‘near taboo’. A pity the world statistics didn’t spare out our ignorance, in fishing out our infamous record. No 1 in prevalence of epilepsy worldwide… Oh cry my beloved country Cameroon!
A big Thank You for your generous donations in cash, kind and goodwill
Isn’t that awesome? Yes we can, Yes we are doing it, Yes will keep walking and marching on in the fight to bring epilepsy out of the shadows.
Dear All, This is a post I did for the Gbm – em blog. Not knowing how to reblog, I copy paste. Thanks for reading:
Hello world, this 10th of October the world celebrates yet another Day dubed Mental Health Day. This year’s theme is ” Dignity in mental health” and this is the focus of our post this week. There may still be more than an entire month to go before the D Day, but the theme is such that we mental health advocates and sympathizers, really need to generate discussions and reflections on this soul searching theme all the time.
The WHO stance
Thousands of people with mental health conditions around the world are deprived of their human rights. They are not only discriminated against, stigmatised and marginalised but are also subject to emotional and physical abuse in both mental health facilities and the community. Poor quality care due to a lack of qualified health professionals and dilapidated facilities leads to further violations.
The theme for this year’s World Mental Health Day, observed on 10 October, is “Dignity in mental health”. This year, WHO will be raising awareness of what can be done to ensure that people with mental health conditions can continue to live with dignity, through human rights oriented policy and law, training of health professionals, respect for informed consent to treatment, inclusion in decision-making processes, and public information campaigns.
A Poignant Public Opinion
We recently came across a blog post by a lady who deplored the ‘indignity’ suffered by her husband who has a mental condition. She makes an arguement that those with a mental health history, are glaringly discriminated upon in hospitals even when they present physical illnesses. She uses a term ‘diagnosis overshadowing’, to explain how the mental illness diagnosis on your chart, overshadows whatever other information is there or could be put there. The medical community seems not to pay the same attention to a patient with a mental health ‘label’ as they would pay to one without. Even if the two came for a similar consultation say of a cardiac problem. This is something we have unfortunately withnessed first hand.
Threats to Dignity in Mental Health
According to an article by the Social Care Institute for Excellence (SCIE),
Research evidence broadly identifies three areas as threats to dignity in mental health care, although there is considerable overlap between them:
We at the Gbm-em Foundation are for a start focusing the bulk of our efforts on contribution our mite to the fight against stigma and discrimination. In our pilot area of the South West Region of Cameroon, these have been brought out by survey to be the main hinderance for any ‘real care’ once a patient or family member starts displaying signs of mental health challenges. There are very few public facilities or medical resources available for such people, there is no mental health policy in place, very limited resources available both to public or private institutions, not to mention the various challenges such families will face in the first place.
Nevertheless, where there is a will, there is a way. For us, it starts with sensitization, advocacy and more outreach. Our campaigns are gradually gaining ground, and our hope is that the more people dare2talkabout it, the more consideration such problems will even attract from the different stakeholders.
I recall receiving this book by mail on the 19th of May 2014, and knew then that it was going to ‘shake me up’. I was still trying to understand what the hell was going on with my brother, and didn’t even know that I was going to understand so much more about my own self too. I had received an amazon coupon from school for a survey I took, and I used it for this and nothing ‘trendy’.
Louise’s story resumed in her words
I was diagnosed with schizophrenia when I was just nineteen. I am forty-three now, and I have recovered – and I use the term ‘recovery’ in its fullest sense. I have been free of medication and free of symptoms for twelve years. I have a husband, a home, and four young children – all things that I never thought would be possible at the age of twenty-five when I was informed of the diagnosis. At that time I accepted what I was told by the medical professionals; that the outlook was bleak in the extreme, that I would get worse as I became older and that I would have to be on medication for the rest of my life.
The Approach of the Medical Community as narrated
I was told that schizophrenia had first been diagnosed when I was nineteen, at the time of the first breakdown, but that it had not been thought appropriate to tell me then. Apparently the condition was confirmed by my second breakdown. Although I was confused at the lack of proof of the illness – there was (and remains) no physical test – I was told that there was no chance of recovery unless I accepted the diagnosis. Then, in a room filled with psychiatrists, psychologists, and mental health nurses, I was told that my life was effectively over. That there was no chance of recovery anyway. They spelled out that I would have to take medication for the rest of my life, and that I would get worse as I got older. The treatment I received in hospital was brutal. Forced medication should in my opinion be outlawed, or saved for the most extreme cases— those who have been violent or suicidal. I was neither. The emphasis in hospital was on containment, not understanding, and this amounted to an inhumane system, notwithstanding the good intentions of some members of staff.
For more on this recap by Louise, read her blog entry shared on Mad In America!!!
What I make of her story
Mental Illness is for real and is sure due to more than one cause. Anyone can be affected and pretending we are fine or stronger than the ‘normal’ person, doesn’t mean we are immune to a meltdown. What begs for reflection is her assertion: “The emphasis in hospital was on containment, not understanding” – aha, is this why stats keep staying so bleak, dark and even dreary? That more and more people get mentally ill and just get worse? And what is the emphasis in society? Who is to blame? Obviously you the sufferer right? You sure brough this embarassment on yourself: Simply put, the Stigma is can definitely keep you really mentally ill. Louise herself admits to smoking cannabis and that is the big cause according to a nurse. Forget about “I was an extremely shy and nervous child. I had a chaotic upbringing – my mother was an alcoholic and my father a gambler. My father was also a very volatile character, and extremely verbally abusive. I found school very difficult – academically I excelled, but socially I was completely at sea…”
Conclusion of this review and introducing it’s sequel
Most of the books I review, are memoirs and I can’t help giving each of them a 5. Five stars to both the Author and the content. The courage, the traumatic experience revisiting all of that, the patience, resilence and all. I just wish such a survival could happen to my dear friend Pammy too. Anyway, stories like these help me just so tremendously in my own healing journey and murdy waters with a sometime frail mental health. I know I am alone in my head and to many, I just not ‘one of them’. Louise Gillett did not just stop at sharing her story, she wrote a sequel to that called Surfacing. She took her daughters to the Mental Hospital and decided to tell them her story herself. I just got a copy of this other memoir of hers, and I’ll be doing another review here in due time.
Louise Gillett can be found via her blog
There are some things which happen and you just don’t think it was sheer coincidence. One of these, was clicking play on a movie called Still Alice. I was on my first flight to the US and didn’t want to sleep on any part of the journey. Movies therefore seemed an interesting option. I watched one called Sideways and then settled next for Alice’s story without paying attention to the synopsis. This is my first review of any movie and I don’t know how I’ll fare. Anyway, am not after a grade, am after sharing with you gentle readers and followers, what I watched and felt with this movie. Let’s start with Alice of course.
Alice the protagonist
She (played by Julianne Moore) is an international linguistic professor, a mum of three, happily married, and ever so ambitious. She is so meticulous with every other thing including her body, which she tones out with an hour’s run every other day. Alice could very well be one of those mothers we refer to back in my country as ‘Mother General’. I am sure many of us will understand this slang even if it were not commonly used in your own countries. Alice and her movie foursome (uh huh she’s married to the cool Alec Baldwin), very well make up that “perfect family” living that “American Dream”. One thing however happens which makes Alice’s story captivating though with a good dose of pity and maybe empathy.
Alzheimer finds its way into Alice’s Life
As in most cases of a neurological, mental or even chronic illness like cancer, it is hard to understand both the “Why, and the Why me”. These questions start replacing Alice’s impressive oratory, as she begins to forget words, places, things and even planned events. She starts to fumble to put it this mildly, leaving her phone and shampoo in the fridge, her medication in the basement, and the thanksgiving turkey to turn to charcoal.
Alice’s life is almost shattered when she gets the diagnosis, and has to share the news with her family. First of all they are in shock, almost ‘shunning’ her, and then it gets worst because one of her daughters takes the test and is positive too. The gene has been handed down much to her chagrin. Alice thinks she has nothing to live for and seriously contemplates suicide by an overdose.
Supportive Family and Alzheimer Association
Alice by now has lost her teaching profession, and is almost losing her sanity. She cares-less about her body, hair or even Christmas. Fortunately, her husband is not prepared to lose her and thus starts informing himself of her condition. He accompanies her to hospital visits and employs a housekeep, then he reassures the family that all is not lost. Alice’s neurologist introduces her to an Alzheimer Association, and she gets to give a keynote address which though brief, is soulful.
It got me thinking
This was the first time I was watching any movie on Alzheimer. I have a dear granny in Israel called Jill, and her husband had Alzheimer. Oh my, is this what she endured? Could this happen to anyone even a highly educated professor of Alice’s caliber? Now, it matters not “why or why me” in the end right? As Alice puts it, Alzheimer brought with it a double ridicule. She felt ridiculous in the eyes of her family ( they wouldn’t believe at first that she was serious about what was going on – her husband said everybody forgets every now and then) and society as a whole, (the stigma and shame and even stares didn’t help), and she felt ridiculous about her own self.
I am not going to rate the movie, I am so touched once more. I am humbled and why not honoured to watch such a movie, and find the need and inspiration to do a review. I hope I have done it justice, but above all I hope that by so doing, I am contributing to the fight against the stigma of such despicable mental and physical conditions. Sufferers need more of love, empathy and support, than even those meds with their drastic side effects. It could be you or someone you love, never say never, and in the meantime make the best of the one life you have…
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