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Tech Test

Tech Test

Test of tech. 

Schizophrenia is syndrome which may include a range of symptoms in individuals including positive, negative, and cognitive. 

Positive: psychotic symptoms  

  • Hallucinations 
  • Delusions 
  • Disorganised behaviour 
  • Disorganised speech  
  • Catatonic behaviour 

Negative mental symptoms: 

  • a seeming lack of interest in the world 
  • not wanting to interact with other people (social withdrawal) 
  • an inability to feel or express pleasure (anhedonia) 
  • an inability to act spontaneously 
  • decreased sense of purpose 
  • lack of motivation (avolition) 
  • not talking much 
  • difficulty speaking due to disorganized thinking (alogia) 

Negative physical symptoms: 

  • an inexpressive or blank face (flat affect) 
  • monotone or monosyllabic speech 
  • lack of gesturing when communicating 
  • lack of eye contact 
  • physical inactivity 

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As someone who’s experienced a lot of social anxiety in her life, I think it’s important to acknowledge that social stuff can be difficult even without the added complications of a global pandemic. Long periods of lockdowns and virtual socialising have given us different expectations and rhythms for how social interactions work. It’s pretty understandable if your social skills are a bit rusty, or socialising feels less natural and weird.  

 

As a general tip, one thing I find helps manage social anxiety is trying to remind myself that there is not a literal, judgmental spotlight on me. If I say make a joke that lands poorly, tell a story that gets a bit boring, or make a faux pas, around 99% of the time there are no real consequences. Most people do not expect ‘perfection’ ‘in social interactions.   

 

If you’re hanging out with people in-person again, I think it’s important to take things at your own pace. Maybe small group settings – a coffee or a walk with one or two people can feel more manageable than a long hangout, or anything involving a crowd. Building in time to recharge afterwards can also help. 

 

But if you’re not comfy with this – that's okay too! Virtual hangouts are here to stay – I know I’m still doing a lot of virtual movie sessions with friends, and texting each other throughout. Spaces like the SANE Forums are great for social interaction too. Online social interactions are just as valid as real ones. 

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Carer Challenges.JPG 

 

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Like me, if you’re a carer you may get frustrated at times when professionals or well-meaning friends and family tell you to “make sure you look after yourself”.  This can often feel impossible and being reminded how hard it can be, can just makes you feel worse right?  However, I think it’s always worth looking at some of the options available to us and be reminded of the things that probably don’t help.  

 

https://australiancarersguide.com.au/ 

 

I came across this article on the Australian Carers Guide website by Mary Bart  chair of Caregiving Matters, an Internet-based charity that offers education and support to family carers.   

DO: 

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Stay connected with your friends. Even a short phone call, connecting over the internet or meeting for lunch will help you feel engaged and balanced, and will keep things in perspective. 

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Exercise as often as you can. Try a regular walk around the block or join an aqua-fitness class at your local pool. Ask yourself this difficult question: “How is my health since becoming a carer?” Feed your spirit. Learn and practice stress-reducing techniques such as tai chi, yoga or mindful meditation. 

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Laugh and keep your sense of humour. Sometimes the funniest things happen while providing care. Acknowledge and cherish those moments. 

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Keep track of the money. Record both what you spend yourself and all financial transactions that you conduct on behalf your loved one. 

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Value your sleep. Always get a good night’s sleep and, if possible, treat yourself to a short break during your day. This will give you the physical and emotional energy you need to get through your day. 

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Know the signs of carer burnout. If you find yourself having limited time or energy, it might be time to take a step back. 

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Be honest and proud. Your work and efforts matter. Don’t be shy to tell people about the valued work that you do. Be truthful with your family about your caring role, your abilities and how providing care is impacting your life (emotionally, physically and financially). 

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Embrace change. Change is constant in providing care. What worked last week or even this morning may no longer be relevant. How well you accept and embrace change is key to staying stress free and being an effective carer. 

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Enjoy the good times. Escape when you can and cherish time for yourself. Take lots of pictures to share and keep a journal to remember the things you did together. 

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Seek and accept help from others. Going it alone is not sustainable. Having the help of others will keep you sane and decrease your chances of resentment, depression and isolation. 

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Limit contact with negative, critical people. If people don’t add value, don’t include them in your day. 

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Learn. Get educated about your loved one’s disability or illness so that you know how best to support them today and what to expect in the future. 

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Take advantage of community services. Numerous community and private services are available, such as adult-care day programs, meal programs, homecare support and respite care for both you and your loved one. 

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Know what you can change and what you cannot change. All we can really change is ourselves and how we react to others and to different situations. 

Here are some of the “don’ts” : 

DON’T 

Let guilt overwhelm you. If you can honestly say that, based on the resources available, you are doing the best you can then your feelings of guilt may decrease. And don’t be afraid to say “no.” It is freeing and gives you more control over your life. 

Lose hope, hide from grief or be angry. Hope gives us a reason to get out of bed. 
It gives us a purpose. Be realistic but positive in your approach. “Anticipatory grief” is the realisation that a part of a loved one is gone forever. Acknowledge it and seek professional help if needed. Don’t let self-pity and resentment control you. 

Stop doing what you love. Keep gardening, reading or going to garage sales. Your favourite activities will take you away to your “happy place.” But don’t overindulge. Eating too much (especially unhealthy foods) or using tobacco, alcohol and other drugs excessively will not only affect your health, but also your ability to cope. 

Try to be perfect. Don’t fuss if some things slide and don’t feel guilty to let them. 

Ignore the signs of carer burnout. If you know you are on the verge of burning out or have actually fallen off the cliff then you need to stop, reassess what’s happening and change what’s not working. 

“Wing it.” Successful caring means being organized, planning and being prepared for doctor’s appointments and meetings at the bank, and creating a dynamic schedule that suits both you and your loved one. “Winging it” is a sure-fire way to fail. 

 

Think you have control over everything and everyone. Although you will be the decision-maker in many situations, you can’t control the health of your loved one, whether your family will offer support or the expense of care. Being realistic will help you stay grounded. 

Expect people to read your mind. Being able to clearly communicate your issues and needs will help others better understand and respond. 

Stop being an advocate. Defend your loved one’s rights and needs. Challenge what seems wrong, does not make sense or will not work. You need to your loved one’s voice. 

Make your care recipient feel guilty. Regardless of how much time and energy you give to your loved one, don’t play the “guilt game” with them. 

Expect your family to pitch in and help. Just because you need and want their help, doesn’t mean you will get it. Life and caring are rarely fair. 

Think that caring responsibilities are equally shared within a family. Assume that one person will do the most, while others will give what they are able. 

Abuse your loved one. Abuse can be physical, emotional and financial. Know the signs of abuse and how to control your anger. Seek professional help and if you’re resentful or frustrated. 

Forget the paperwork. Paying bills, filing annual tax returns and insurance claims, and keeping cards/ driving licenses current can be time-consuming, frustrating and expensive if neglected. 

Share everything. Be guarded with what you share with your friends. Understand that most people don’t want to hear or know it all. Giving too much information is not a good thing. 

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For those of you who aren’t carers or are looking to give others some tips on how to support the carers they know, here are some great tips from Mary. 

 

 

AVOID THIS TO: BE A REAL FRIEND TO A FAMILY CARER 

Trying to fix the situation. 

 

Supporting your caring friends does not mean that you are responsible for solving their problems. These issues are out of your hands and may actually not be solvable. Be aware that when you try and change situations, you might actually complicate them. 

 

Offering unsolicited advice or criticism. 

 

Don’t think that you add value to a carer by being critical or saying that you have a better way of doing things. Keep your comments to yourself about how they are managing care. You are not their boss or even their peer. A “know-it-all” attitude might well be met with resistance and even drive a wedge between you and the carer. Instead, praise the carer for something that you genuinely think they are doing well. 

 

Adding guilt. 

 

Carers live with mountains of guilt. Don’t make it worse by piling on more. Nagging a carer is not only unproductive but highly unsupportive. 

 

Saying unhelpful things. 

 

“You have gained a little weight and what’s with those bags under your eyes?” “What do you do all day? 
You should get out more and take better care of yourself.” Say kind and comforting sentences. “Thank you for doing all you do.” “I’m coming over on Thursday afternoon to watch your mother while you have a nap.” “I can’t image how hard it is for you to watch your dad in so much pain.” “I wish I were there to give you a big hug.” 

 

Being a stranger. 

Don’t think that you are bothering a carer by phoning or dropping in. Such social interactions are absolutely critical to their well-being. If you call at an inconvenient time and are asked to phone back later, don’t take it personally. 

https://www.youtube.com/watch?v=EoDeWqJOtRY  

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I came across this article on the Australian Carers Guide website by Mary Bart  chair of Caregiving Matters, an Internet-based charity that offers education and support to family carers.   

 

DO: 

Stay connected with your friends. Even a short phone call, connecting over the internet or meeting for lunch will help you feel engaged and balanced, and will keep things in perspective. 

Exercise as often as you can. Try a regular walk around the block or join an aqua-fitness class at your local pool. Ask yourself this difficult question: “How is my health since becoming a carer?” Feed your spirit. Learn and practice stress-reducing techniques such as tai chi, yoga or mindful meditation. 

Laugh and keep your sense of humour. Sometimes the funniest things happen while providing care. Acknowledge and cherish those moments. 

Keep track of the money. Record both what you spend yourself and all financial transactions that you conduct on behalf your loved one. 

Value your sleep. Always get a good night’s sleep and, if possible, treat yourself to a short break during your day. This will give you the physical and emotional energy you need to get through your day. 

Know the signs of carer burnout. If you find yourself having limited time or energy, it might be time to take a step back. 

Be honest and proud. Your work and efforts matter. Don’t be shy to tell people about the valued work that you do. Be truthful with your family about your caring role, your abilities and how providing care is impacting your life (emotionally, physically and financially). 

Embrace change. Change is constant in providing care. What worked last week or even this morning may no longer be relevant. How well you accept and embrace change is key to staying stress free and being an effective carer. 

Enjoy the good times. Escape when you can and cherish time for yourself. Take lots of pictures to share and keep a journal to remember the things you did together. 

Seek and accept help from others. Going it alone is not sustainable. Having the help of others will keep you sane and decrease your chances of resentment, depression and isolation. 

Limit contact with negative, critical people. If people don’t add value, don’t include them in your day. 

Learn. Get educated about your loved one’s disability or illness so that you know how best to support them today and what to expect in the future. 

Take advantage of community services. Numerous community and private services are available, such as adult-care day programs, meal programs, homecare support and respite care for both you and your loved one. 

Know what you can change and what you cannot change. All we can really change is ourselves and how we react to others and to different situations. 

 

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Suicidal thoughts are not uncommon but are often concerning to hear. While it can be challenging to understand, some people believe they are a burden on others and think their loved ones would be better off without them. People who feel suicidal are experiencing intense emotional pain. They want to stop this pain and see suicide as an answer.  

  

People may talk about suicide directly (e.g., talking about a plan to take their own life) or indirectly (speaking abstractly about death or referencing suicide in media or art). Any statement about death or suicide must be taken seriously. I know it’s hard, but it’s important to talk openly about suicide and suicidal distress.  

  

A lot of people think that talking about suicide will increase the chance of people acting on it. Talking about suicide may reduce, rather than increase, suicidal ideation. Opening this conversation helps people find an alternative view of their existing circumstances. If someone is in crisis or depressed, asking if he or she is thinking about suicide can help, so don't hesitate to start the conversation. 

  

Being open about suicide also helps to reduce stigma, supports help-seeking, and reminds them they are not alone.  

  

If someone is in immediate danger, please call 000 or visit your nearest hospital emergency. If you're worried about someone's immediate safety, make sure someone stays with them until you can get help.   

  

For more information on supporting someone with suicidal thoughts, you can contact the following services: 

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There are a LOT of symptoms that can be caused by perimenopause some of which I have already mentioned like hot flashes which is the one most folk seem to know about.  

  

Here are some others which don’t get talked about much: super-dry skin, hair loss, insomnia, joint pain, avalanche of overwhelm, painful sex or changes in how your vagina feels, ‘brain fog’ trouble remembering things or finding words, night sweats, rage, ‘flooding’ where you bleed a lot, more than a normal period. Some people have to stop or pause their usual activities because of the volume of blood, leg cramps, and waking at 3am etc.  

  

While hormonal fluctuations can impact on our emotional and mental health it is super important to acknowledge, at this time in life, women are expected to do an awful lot of emotional and physical labour. We are often responsible for other people, caring for children / teenagers, ageing parents and working. So, when we feel like we’re “loosing it” are “all over the place” and “emotional” – yes it could be menopause but it can also be the circumstances and situational stressors which are happening and very real having a massive impact. 

  

As you can imagine all of these symptoms can have an impact on us not just physically but also emotionally. 

  

At each stage of life and when experiencing any physical or mental changes it is always important to check in with your GP. Before going along write down your symptoms and any questions you would like to ask. When there write down any information the GP offers which you would like to remember.  

  

Perimenopause is also a good time to get update to with all your health checks too. Blood tests, cervical screening, and breast examination etc. 

  

It's not uncommon for GPs to not know a lot about caring for people in peri-menopause and menopause. Don’t allow any GP to dismiss or minimise your symptoms and what you are experiencing. Don’t be silenced, channel your inner Enchantress (who is she you ask, we will get to that I promise) and continue your quest for answers elsewhere. 

  

Listen to your intuition you know your body. If a GP is unable to assist or if you don’t feel comfortable with their response you are within your rights to seek another opinion or seek a referral to one who specialises in Menopause care. 

  

There are loads of resources around on Menopause some of which I will post links to a little later in our chat. Find out as much as you can this will help you to advocate for what you need from your GP. 

  

People in the midst of perimenopause, particularly if they are not aware that is what is going on might feel alone and confused. I know this was certainly me at times! 

  

There are benefits to menopause of course. No longer menstruating can come as a relief from physical and emotional symptoms and can mean extra money each month not being spent on sanitary products and contraception.  

  

It also can signal a time of greater sexual freedom free from worry about falling pregnant. 

  

We can look at menopause as part of a bigger story, as just one of the transitions and roles women come to on their journey through life. A role that has value. 

  

The phases of a woman’s life can be depicted in the following way: 

  

Hang on, before I get into describing this particular way I would just like to say it is an offering it may or may not resonate with you. 

You might have your own words for these phases, or perhaps these phases don't fit your experience - that's ok. It's important to say that different cultures also understand the phases of women's lives differently. These phases below are ones we sometimes see in Western culture, but even within that there's variation. There's no one way to go through life as a woman. If these ideas don't resonate for you, don't feel you need to take them on. 

  

Perhaps you might like to share the phases you relate to - feel free to share them here!  

The journey as an adult begins with the -   

Maid – representing youth  

  

Mother – can represent either actual motherhood or the caring role women are expected to play  

  

Enchantress – no longer tending to small children, experienced, wiser with more time and able step in to their power.  

  

It is little wonder physically at this stage many experience heat in the form of hot flushes and for some rage and anger.  

  

A lot of people we have spoken to at this stage and beyond talk about no longer being willing to put up with any BS. 

  

Crone or Wise Woman – The final transition is to the Crone. A Wise Woman who has a lifetime’s worth of learning and experience and a view of the bigger picture.  

  

Like all life transitions, you come out the other side still yourself but changed…an updated version of you. 

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@amber22 wrote:

 

The journey as an adult begins with the -   

Maid – representing youth  

  

Mother – can represent either actual motherhood or the caring role women are expected to play  

  

Enchantress – no longer tending to small children, experienced, wiser with more time and able step in to their power.  

  

It is little wonder physically at this stage many experience heat in the form of hot flushes and for some rage and anger.  

  

A lot of people we have spoken to at this stage and beyond talk about no longer being willing to put up with any BS. 

  

Crone or Wise Woman – The final transition is to the Crone. A Wise Woman who has a lifetime’s worth of learning and experience and a view of the bigger picture.  

  

Like all life transitions, you come out the other side still yourself but changed…an updated version of you. 


This is interesting