2am and Im awake again, another 1.5hrs sleep before I wake up like Ive been asleep for the past 8hours. Its short lived though, it wont be long until Im tired again and I want to go back to bed.
Normally my GP does my sick certificates for one month at a time, however she has done the last one for two months, which is odd, Im not sure why she has done it but no big deal. It does however take me to nearly 11 months off work. I said to Dad about it and he said that would be a year off, he loves to round up like that. I then got onto the reality that its going to be longer than that before I return to work. As it stands, it would appear my treatment protocol will primarily be physio/exercise pshysiology based which means it will be a while before there is improvement in my pain, improvement that sees a continual reduction in pain. Im also going to be going through a reduction process for my pain medication. Both things are going to cause me some level of pain, at least in the begining and if I cant deal with the pain Im in and work, how does he expect me to work and deal with an increase in pain. That said I am only guessing what the neurosurgeon says, what treatment protocol I end up on. I want to go back to work and as soon as possible but it makes no sense for me to go back and then be having time off because the pain is too much from treatment or my excersises etc. and not have an income at all. So, until its reasonable for me to go back, Ive made some decent strides in recovery etc. then Ill have to stay off workfro my own financial well being, not just my health.
Boy writing the above was hard work, I kept dozing, I started feeling quite awake, then it was like I got hit by extreme tiredness but I had to finish what I was writing. Now, its like Ive been asleep for a while and Im ok again.
With everything healthwise Ive been dealing with I wish there was a device that they could put you in that scanned you and just spat out a report of all the things that were wrong with you and I could get a complete list of issues so we could treat them the best way possible and there wasnt all this back and forth, working out if symptoms were medication related or actual issues to deal with. Not to mention the delay in testing, results and treatment. You went into a doctors appointment, you were assesssed and treated all in one sitting.
Ive had some tests that have provided results, provided information in relation to why Im in the pain I am. My GP has gone through the results with me, but its not up to her to determine the treatment protocol for my conditions, that, I hope is up to my neurosurgeon. I really hope he doesnt turn around and refer me to someone else, which he could. He might decide its outside his field and send me to a pain management specialist and it wouldnt suprise me. But I feel like I am one step away, a 15 minute conversation from this is how we treat your situation and yet I have to wait for so long, approx another 3 weeks for that appointment. It really sucks, to be so close but so far.
Im going back to bed in a minute, Im not dozing like I was but I need to try and get some more sleep, its 4am. Trying to work out how much sleep Ive had in a 24hour period is getting to be impossible, Im just up and down like a yoyo but I want to finish my bankruptcy stuff tomorrow so I dont want to be sleeping through the day. I have to ring one of my creditors to find out how much I owe and get in touch with a lady I have called my Auntie my whole life as they need someone who knows me that doesnt live with me, so Im going to ask her if she would mind being that person. I think if I can get those two pieces of information then I should be able to finish it and submit it tomorrow. But if I sleep all day I wont be able to.
I went to bed around 4am and Ive just woken again a bit after 6am. Once Ive woken up properly Im going to go into town and do some grocery shopping, Im not really looking forward to it, if it wasnt really needed I certainly wouldnt be doing it. I know its going to be painful, Im already pretty much in a decent amount of pain. I know adding walking of any distance to things is going to make things much worse and do so really quickly. In the short time Ive been up the amount of pain in my back has increased dramatically. Its gone from ok, a little uncomfortable to pretty painful in like 15 minutes of sitting down. Im not far from needing pain relief just to manage sitting, let alone shopping.
It doesnt matter what or how much I drink at the moment, my mouth feels dry, like Ive got a mouthful of cinnamon powder or something. My tounge is sore but not as bad as it has been. Its more that my whole mouth is dry, more than dry.
Im really hoping to accomplish a couple things like the bankruptcy submission, today. I have accomplished stuff lately but medical scans and tests are not really the things I want to accomplish. I dont suppose filing for bankruptcy is high on the list of things I want to accomplish either, but it relieves a lot of stress, its more than that because I dont worry about my non-family debts that much, if I do nothing Im going to be default listed and potentially sold and Ill continue to be contacted etc. whats the big deal. Going bankrupt puts so much to bed, it finalises so many things. It takes 3 years, there is stuff I have to do and provide but predominately its the end of things for me. Debts that have haunted me since I had my brief psychotic episode are all but gone.
Im going to go do this shopping before my back gets worse, Ive been putting it off but thats not really going to help. That wasnt ideal, I managed the servo with no issue but by the time I got to Coles I had started to feel quite wonky, it was a 10min job at Coles so I figured Id do it and come home. I went through Coles, got the couple things I normally get and went to the one open check out, normally not an issue but at this hour of the day they only really open the express lane, which had a small line up, but the cashier was friendly and liked to chat, worse still the person in front of me was the owner or manager of a store within the complex, so the chit chat was even more. By the time I got to unpack, my pain was really bad as was the wonkyness. As soon as I paid and left the store I made a b-line for the nearest seat and sat for a while. It helped calm my back down a bit before I tried to drive home, the hassle was the wonkyness. It was a slowish drive home, I was stuck, Dad was home without a car, there was no help coming so I was on my own and needed to get home. I really didnt anticipate that Id be hit as early as I was, I didnt have my meds until late last night so I assumed, incorrectly that I would be fine until atleast the normal time I have my meds in the morning. I got home ok, unpacking took a while. I brought in the stuff from the servo and then went and had my meds and sat down for a bit, again my back was really sore so I needed to let it rest a while. Then I went and got the stuff from Coles. However everthing is still in its bags, I havent got to putting into the fridge etc.
Im going to go to bed for a bit, its 10:30am going by history Ill be up again by noon. Im seriously drowsy, I have no choice but to go to bed. I did the SANE survey and some other stuff but the last bit over an hour sorta disappeared on me. I have no idea whats going on with the show Im watch Im watching, typically I have no problem doing both. So Im assuming I had fallen asleep.
Im up again, I slept for a couple hours, apparently quite soundly because I didnt hear my phone ring twice, this whole sleep thing is really getting to me. I have no pattern, I sleep so heavily sometimes and so lightly others times and generally the way around that it matters ie today sleeping through phone ringing. Despite all of this Im still so damn tired, constantly. I cant catch a break on that front. Ive just woken up and Im really tired, like its difficult to keep going and pushing forward with what I need to do.
Just before I went to bed, Dad said that my sister was on the way up, I had no choice but to go to bed anyhow. I was falling asleep as it was. When I woke up she had been and gone, I had hoped Id see her, kinda of. She is not going well at the moment and lashing out, not seeing her means I missed out on all that and I cant say Im upset about it. I couldnt and wouldnt deal well with that at the moment. Apparently it wasnt the most wonderful visit for Dad, he got in shit for all sorts of stuff, my sister told Mum about things Dad was doing or trying to do which got him in shit with Mum and she asked for more money from Dad for stuff for Mum, but she was asking for far more than what the stuff for Mum actually cost. Dad keeps handing over money to my sister in one form or another at the moment and he has had enough.
I just got a call back from the dermatologist I want to see, it will be 3 months before I can see her. Im going to try and see what another place is like at the moment and if I can get into them sooner. Waiting 3 months seems kinda excessive. I rang the other place and they have a long wait too so Im sticking with the doctor Ive organised things with.
For whatever reason, my legs are really sore, its not the same as when they are full of fluid. They are swollen, they have been getting swollen more recently but it doesnt feel like that. I had the same thing last night at one point. Im not racing off on it, its probably bcause Im exhusted or something like that.
Ive all but finished the bankruptcy form, Im just waiting for a family friend to let me know if she will be the contact for them and then Im done. im pretty sure its been done right, I suppose Ill find out soon enough. Im updating my families medical history as well. Mum has her sides information but very little is known about my Dads side. Dads side isnt close, I havent seen any of them that I can think of since my Dad's Mum passed away and that was many, many years ago. Mum and Dad thought the best chance of getting that information I had was my Auntie on that side of the family, Dads brothers would have no idea either. So I have msged her and asked, she sent a message back saying she will look into it and let me know. Im going to work through the information Mums provided shortly, though I would kinda rather go to bed lol.
Im a big believer in equality, I believe that on the provision that it doesnt impact my right to do the same, everyone should be allowed to live and believe as they want. I dont care who or what you do in your bedroom, I dont particularly want to know. On the provision that its legal and both parties willingly consent why should I care. I really dont think that people should be treated differently to anyone else based on this, or anything for that matter really. I dont have an issue with events that work towards highlighting and changing societies attitude towards relationships that society defines as not the norm. I dont believe however, that their expression of love, who they love should be enforced upon others, just as much as any other form of expression. Love is love no matter genders etc. Gender expression and acceptance is difficult, again, I dont care what gender you are, if I get your pronoun wrong gently correct me, thats not an issue, however attacking people for not getting it right doesnt help anyone. There are a number of genders people fit into, for many there were just the male and female growing up and most our life, we were never exposed to anything more, not because we are ignorant but its all we knew, its all anyone knew. If you correct, with love and they continue to address you incorrectly then I understand being offended. But dont just assume that people a) are going to know your sexuality or b) your gender.
I believe the way women in general have been treated and had limitations forced upon them is wrong and has been a huge mis-service to society. Over the years who knows how many amazing discoveries have been lost because society forced women into a preset box of what they could be, what they could become. I hate what was done to those with mental health issues in decades past but what was done to women under the guise of mental health is appalling. On a whole women are just as capable as men, there are some women who would not be able to keep up with some men physically, but the same can be said about men, there are some men that would not be able to keep up with other men or even some women. Each individual has their own strengths and weaknesses, both physically and mentally, that makes them suited to different careers and hobbies, regardless of gender and thats what should be considered. I dont agree however with the current stratergy of many businesses of having required percentages of women in different positions, even goals etc. That is first and foremost reverse sexism, it is giving women a higher priority for employment over men. Secondly, it puts the company at a disadvantage, a male hirer might be the better choice but not the best choice gender wise, so which way do we go, which priority it elivated highest.
How we treat the disabled, the mentally ill and elderly shows who we really are as a society. We have become a society that only values its people on the provision that they are benefiting society in some fashion. The elderly made the country what it is today, they went through massive hardships, hardships we will never understand. They fought against amazing odds and overcome to rebuild the country etc. When it has come to the end of their lives, their final years, they are put into aged care facilities, stripped of their individuality and choices and made to eek out an existance until they pass away. I dont understand why you would ask an 80 year old to stop smoking, or make it hard for them to do so. If they have got to that age as a smoker, let them do as they please for the final few years. The same goes for drinking, if they like a drink with tea, before bed etc. then let them, Im not suggesting allowing them to get hammered every night, but whats the harm in allowing that on occassion. It would be about liability, if they fell over and they were hurt etc. The same goes for disability and mental health, society makes, they force the disabled to be burdens on their families. The support provided to look after a person who is disabled is pretty pathetic. Not to mention the same if you are the actual one who is disabled. I get you get a health care card, but that doesnt help with so much, specialists etc. Somehow, people on DSP have to find a way to afford these things on an income that only barely covers their costs of living, it doesnt take into account their costs of being unwell. The treatment of mental health issues is almost worse than the illness. My sister and I tried on a number of occassions to get her help before she attempted suicide. They wouldnt even see her, wouldnt talk to her, anything really because she hadnt attempted. How dumb is that, prevent the illness escallating to a potentially lethal outcome if given the opportunity. Treatment for mental health in the form of psychology is only partially supported by medicare, 10 sessions a year, even for one issue your only just starting to get into the actual treatment phase before support is withdrawn leaving so many incapable of continuing with treatment until the following year, where they basically start a new and the cycle continues, just support mental health treatment and have no limitations to the number of visits allowed. Try getting a bed in a facility and not be critical, even if your critical your going to struggle. Services that are available are stretched and often provided by the charitable arms of religious groups. If you have an adversion to religion, even though they dont push it within the confines of treatment, you might not access those services because of what the church has done to you etc. It would seem to me the two biggest groups involved in treating those with mental illness are the two biggest groups who have hurt those with mental health issues in the past, government and religion.
The treatment of our first nations people is appalling. What was done by European settlers was just inhumane, however the fact that Australia continued to treat them the way it did for so many decades is just horrendous and to this day, we continue to fail them on a whole, we continue to treat them as if they are not worth equality. I dont believe however that giving one group a greater say in the direction of our country is the right answer. More so, that we would be asked to vote on this concept, what to me seems like an incomplete concept, isnt right. Firstly, give us the complete picture of what their authority will be, is it just that they will put their 2cents in on everything, then why, how does that actually help etc. Secondly, Im about equality, I dont believe a group should have a greater say or infuence on things than any other group and where does it stop, do we start having different groups assigned to different aspects of discussion and government? I believe we should however work with our first nations more, not impose upon them as we do. We keep giving them and making allowances for them, in an attempt to make them more like us, but maybe thats the wrong approach, maybe we should learn from decades of trying to convert them to the way we do things and allow them to stand up and do things the way they believe to be right, of course we would still need to ensure they are safe, that they have access to the same services as everyone else but we should make their chosen way of life acceptable in our overall society.
Discrimination in all its forms is just wrong and needs to be eliminated completely. A person should not be judged by their skin color, religion, creed, chosen life style. I think Im just against hate, unjustifiable hate. Someone does something horrible to you, you might hate them, thats one thing but hating someone because they are different to you thats, I dont have words. Our differences is what makes us truely valuable. If we were all identicle in every way, then we could not grow as a society, as people. We would make no discoveries, we would have no desire to explore. Being different from one another, we see there is opportunity to experience life differently and to seek out more that is different from us.
If we understood that our differences are what makes us valuable and therefore what makes others valuable then we would eliminate all forms of discrimination because we would be too busy embrassing the differences of others, learning from them, building a society that seeks out differences and grows as a result.
Im incredibly tired again, Ive been up for few hours and here I am ready to sleep again, almost desperate to sleep. I went and had a shower, for much of my shower I am simply sitting letting the really hot water run over me and down my back. We are on rainwater only, we have a huge tank so we rarely run out, if we do we have bore water as a back up. So water costs and being economical with water isnt really an issue. FYI, I just hallucinated a blue ring octopus on my keyboard, thats a new one. My sister isnt doing well at the moment, neither is my Dad, probably none of us are but yeah. Anyhow, she came up today and Dad isnt in a good mood and it was an issue that he didnt seem happier to see her. The fact that the last couple of days all he has done is try and organise bills of hers that she has ignored, trying to avoid her get in shit. All she had to do was upload the bill to her health insurer and they would have paid it. Now it is a huge deal, a massive ordeal for Dad, because my sister has gone and thrown her hands up and walked away. But she can still organise to buy this and that on Buy Swap Sell, order stuff online for Dad to collect from the postoffice. There is so much my sister likes to do and magically can do for herself, but dealing with the requirements of being an adult, real life shit, she just ignores it until its almost too late and then makes it Dads problem, generally by winging at Mum. Time and time again, this sorta shit happens and time and again, Mum buys it and wonders why she feels alienated by me and Dad. Hell, Dad went out with a couple of guys from work, one brought his girlfriend so Mum has the shits on that Dad didnt invite her. They are seperated, which Mum instigated, she doesnt get to have an opinion as to how Dad reacts about that. She clearly cant stand Dad, doesnt want to spend time with him normally, she doesnt come out her room, pretty much ever, seriously, what do you want. Added to all that, and he is quite entitled to have, these are his friends, he would talk about home with them, he might not want her in that space, not to mention that Mum has a tendancy to make herself the absolute focal centre in these environments, she would take over completely, shut Dad down at every opportunity, maybe, just maybe Dad wanted some time for himself, to recover a bit, for it to be about him for a while, not someone else.
There is a few other things we talked about but the one thing that really got me is my sisters support person. She has been awesome to my sister, she helps her so much, she changes times and is there for her at the drop of a hat. My sister relies on her so much and rarely does she not come through for her. My sister had organised her to take her to an appointment tomorrow, but the support person has had to pull out because she has a doctors appointment now for herself. Well why didnt she make it for a time outside of when my sister needed her, now my sister, who has a car with her, has to taake herself, she has to pay for the fuel to go, you know the $10-$15 its might cost. Now my sister cant really rely on her support person, who knows when shes going to pull out. How dare she have her own life, how dare she be sick herself. For all we know the support person she might have found a lump or something and be freaking out and this was the first appointment she could make to get it looked at or she might have been waiting to get into a specialist and they had a cancellation and she can get in sooner. What ever the reason, she has an appointment for herself that she has decided is more important than WORKING. My sister is this woman's job, she is not her parent or anything like that. She is pleasent to my sister, she is friendly to my sister, she helps where she can, even thr drop of the hat stuff, she does all of it because my sister is her job and she wants to keep that job. My sister is worth something to her, something financial. My sister likes to impose a relationship beyond this but fundementally there isnt one. The support person might like my sister, she might care for her and everything else, but at the ed of the day, she is how she pays the bills. Its the same with her GP. Her GP cares for my sister a lot, I can see that. She goes out the way for my sister, etc. but again my sister isnt her daughter, she isnt her friend, her GP didnt come and visit her in hospital, she is her GP first and foremost, caring for her comes with the territory. She is her GP's job, this is how she makes a living. She does it time and again, she gets attached to her medical team members, if she doesnt have this deep connection with them, it doesnt last, then and pretty much everytime, the medical person acts like a medical person, they make a call my sister doesnt like or wont do a surgery my sister has decided she has to have. They take time away for their own needs. They move or their time with my sister ends and eventually they tell her to stop contacting them. She creates a deeper relationship with these people than there is, than there ought to be. If I am paying you to spend time with me, for what ever reason or you are being paid to be in my vacinity (ie work) we are not really friends. A friend is someone who spends time with you for its own reward, they enjoy your company and that is sufficient reward. You can be liked, you can get on well, you can have conversations and have a different relationship with you than what they have with their other clients, but you are still a client, you are still paying them, until they offer their services for nothing, not even bulk billed, just as friends then you are not friends, you are in a commercial relationship and my sister cant get that. It drives me fair batty that this is the case. What I find really appalling, really frustrating is my Mum supports how my sister is feeling, like she is telling me about her support worker taking time off to go to the doctors in disgust, she is fully onboard with my sister, she is supporting my sisters point of view, her attitude, she isnt correcting her. Which would be why my sister hasnt contacted me and winged about it to me, she knows I would tell her to pull her head in. I didnt say anything to Mum, Im too tired and too sick and there's no point, it wouldnt get back to my sister, it wouldnt change my sisters attitude so whats the point. More and more often I am getting to this point that its just no point saying anything, so I pick and chose when I speak up, not that Im afraid of wasting my time, its more so I dont want that everytime I go see Mum that I am having a fight with her.
Im going to go lay down and try and get some sleep. This sleeping for a couple hours and then being up for a bit and repeat is getting old and funnily enough tiredsome. I dont feel well either, Im still having fluctuating tempretures, not as widly fluctuating though. My stomach still hates me, I dont have diarrhoea but its really loose and I feel like I need to go almost all the time. I have a headache going almost all the time and ofcourse Im constantly tired, more than tired, its this perpetual exhustion. Everything aches, my back is really sore, Ive been taking extra pain medication today, well last couple of days. The continual struggle is really getting to me, as much as I try to I remain positive and keep to my core beliefs about myself etc. But Im finding that hard today.
I laid down but it took what felt like ages for me to fall asleep, by the time I stopped what I was doing I had perked up a bit, which happens and why I dont think its really that Im naturally tired. It either goes like that or I keep dozing off. It wasnt like a great deep sleep either, it was really light and I kept waking and falling back asleep. I do feel better now, I was in bed for 2.5hrs, though a bit of it was trying to get to sleep. It didnt help that I was pretty frustrated when I went to bed, I did have thoughts swimming for a bit. Just the stuff above, the stories from Mum and from Dad, how they can never marry up. The annoyance I have with Dad saying things like "whats the good of you" when I dont know the answer to yet another question about something I would have no knowledge about. I know he means nothing by it, well I think he doesnt, but Im stuck sitting watching TV all day, writing and going to doctors appointments, I cant work, I cant help him, I dont really feel that I am much help to him, so when he says stuff like that, it stings.
I did finish my bankruptcy application today, it will take around 4 days for it to be processed so all going well, Ill be bankrupt early next week. Im still having mixed feelings about it, I know I have no other choice, I recognise that I should have done it a long time ago, it would have been so much better for me. But I feel like I have given up, that I have let someone down, myself included. That somehow irrespective of the facts, I should have been able to manage everything, because thats what has always been expected of me. Ive always been expected that somehow I should just be able to manage without any help or instruction how to do these things. It is like being thrown into the deep end of a pool and expected to swim perfectly with no previous instruction or knowledge. Dad said once, probably more than once, that his parenting style is to let us try first on our own and if we dont succeed then come along side and teach, which kinda makes sense for some stuff I suppose, but its pretty dumb firstly because he never came along side and helped when we failed. But, something like our finances there should have been more effort put into making sure we understood that world, particularly given we were taught how to look after our money using cash, we would have bills put out and money would be put on top from each pay so that by the due date we had enough to pay the bill. Everything was paper and cash. I could see it. Translating that to the electronic world is terribly difficult for me, I cant see what I am spending, its just tapping a card the value of the transaction is gone, I spend $10 or $500 its just a tap, psychologically there is no difference for me. Bills are paid automatically via direct debit, Im not involved in anyway unless there isnt enough money in my account. I rarely know my account balance, no idea, I used to just look in my wallet and Id know how much money I have. Ive tried putting bill money into another account, Ive even gone as far as having accounts for each bill making a digital version of the old way of putting cash onto bills. It doesnt work, its so simple and so quick to transfer the money into my main account to pay for something I see as more pressing. In the old days of cash, if I decided to spend my bill money on something, I would have to go home and get the money, then go back and buy what I wanted, in the mean time the impulse died away etc. There is also the physical act of taking the money from the bill it was assigned to, it had more of a psychological impact on me. Mum isnt a great example to live by, she doesnt care what she spends, Dad has to work it out in the end and when they dont have the money she expects them to have, she blames him for mis-managing the money. My sister treats things very similarly, when she doesnt have the money, Dad will just have to cough it up. Ive borrowed from Dad before and currently owe him money but I never expect it of him, its always a request, always humbly made. My sister its a demand, if she doesnt get her way, she goes to Mum for Mum to argue with Dad. I cant seem to, for all of my fondness of the modern age and technologies, I cant get my head around dealing with my finances within this new environment, I miss and prefer much of the old ways of things.
On the subject of money, Mum has an account with quite a bit of money in it, which I dont have an issue with, but its been done or atleast maintained by taking advantage of my Dad. She has this money aside for her security, for incase she has to escape. She acts like Dad beats her and she might one day have to run. He might not treat her the nicest, he might not be the most attentive, though I think given the circumstances and everything she is really lucky that she married him because almost every other male on the face of the planet would have left her, left her many many years ago. She has plenty of flaws and issues, she treats him like shit and has for as long as I remember. Their relationship has been pretty volitile over the years, she had no problem yelling at him and ripping him to shreds. My sister says she doesnt remember her childhood but doesnt accept that Mum was like this or if she wasnt like this she was crying. She does accept Mums claim that at the early part of their relationship Dad hit her. Dad says he doesnt remember this, interestingly I apparently attacked my sister and I dont remember that. Thats kinda interesting and I never thought of that. That said, Mum does admit early in their relationship she cheated on him, he apparently knows about it. It was a twisted conversation, but I think at the end of it she was blaming my Dad for it happening because my Dad didnt protect her from him. Then, when Dad has an issue with her having young guys coming around at all hours of the night, with 2 young kids trying to get some sleep, as well as him for work, she doesnt think he should have a problem. I would think if there was a past cheating event, it would not be unreasonable for Dad to be aprehensive. Anyhow, she has this money stashed, she talks and acts like she is the victim of continual abuse etc. She even talks like that to her sister, who was abused by her first borns father and she did leave, she lived off a pension, she got no support from his father. Their situations cant even compare. Mum keeps that money in her account by making Dad pay for as much as she can get away with. She gets DSP, so she now pays for her smokes herself, everytime she asks for them and Dad goes to get her card to pay for them, she makes a face or a comment as if he should pay for them, even occassionally. Even though he actually does, but there again why should he. He wants her to stop for her health, why would he happily support her in doing so. He pays for the running of the house in its entirity, he pays for her food, everything. She has this money, she has an income and she still pushes as much responcibility onto him as she can. Even when it comes to supporting my sister. Dad said he will cough up $2k to my Mum to help, above that she has to pay it herself. Last I heard she was demanding Dad coughed up $3k. I dont understand why Mum cant hand over money to my sister out of her money if she is so desperate to keep giving my sister money hand over fist.
I spoke to Dad tonight, I voiced how Im a fair bit ticked off that my Mum is moving hell and high water to make sure my isnt getting overdrawn fees and I filed for bankruptcy today and to me thats just flat out disgusting. Mum has at no stage, from the moment I had the brief psychotic episode and came home Mum had done nothing to help me with my finances at all. She knew, as well as Dad, that I wasnt managing my rent. From that you could deduce that I am probably not managing other obligations. But she will point to Dad as not coming around and helping before it got to bad, she didnt either and thats the theme of things for me. Be it that she left me for Dad and thats enough for her, but for me, its not. She knew Dad wasnt helping, that he was letting things build up and she chose to still not do anything, she is as responcible as he is. I was incredibly sick, I was on some serious medication and could barely make heads or tails of life let alone bills and rent. But my sister cant get even an overdrawn fee, she ignores bills and its Dad who has to fix it, even to blame because he should have helped, even though he didnt know the bills existed.
Its been a pretty huge write today. Ive had a fair bit on my mind. Ive realised too that talking to Mum and Dad seperately, has turned a bit sour. Its far less talking about random stuff, anything, its become all about talking about Dad, Mum or my sister depending on who Im speaking to and what they are doing wrong, how they are a disappointment, how they dont do enough, how enough isnt done for them. The number of conversations Ive had that have left me feeling like absolute shit because Mum has this belief that my sister should be treated so differently to how I am. My Mum will go on about Dad having gender biases, Im a guy, my sister is a girl so we are treated differently, Mum is no different, maybe worse. My sister is a woman, so Dad should look after her, financially etc.
Im really not well, I started the new anti-psychotic but Ive also started a new anti-biotic, on top of being on a few different types anti-biotics over the last very short period of time. Not just being on an anti-biotic, I was on really high doses at times. Im taking a probiotic to help, this is a first for me too. Its not overly suprising that I dont feel well, not to mention that Im normally not terribly well to start with. Ive had moments where I was sure if I opened my eyes or moved I was going throw up, I literally got up, took a step and it hit me. I have days where Im going #2 a fair bit, not diarrhoea just needing to go more. I feel like I have to go more often than I do actually need to. My stomach is generally all kinds of topsy turvy. I have this stupid headache that just keeps pounding away. My body aches more often than not, like really aches. My legs are almost constantly sore, as are my feet. Then you have my normal crap, such as my back which has decided that it wants its voice heard again. Its not loud yet, but its making its way to it. My shoulders are being an issue quite often, the left has really been problematic. Its hard to lay down to sleep when both shoulders are angry. My tounge, God my tounge drives me round the bend. Im going through antiseptic mouth wash trying to calm it down, not trying to fix anything just make it bearable to live with. Dealing with boils is a challenge but the latest anti-biotic is actually helping in that battle. Theres still a few about and they are in spots I tend to sit or put pressure on, so they are annoying but the angryness is gone for the most part, they have lost most their bite, which is really nice. The dermatologist I am booked to see are taking appointments into June next year but they have pushed me to Feb, which is a relief, but still a long wait. My tempreture movements are concerning me a bit, like Ill take my temp and its 36.6 and 30min later its 37.5. That to me seems to be a thing for concern, I am going to speak to my GP about it, unless I do see it hit 38 or above in which case Ill speak to the ER doctor about it. I think the hardest thing is my sleep though. Its like I get tired randomly and I go to bed and get 1.5-2.5 hrs sleep and then Im up again, when I wake up I cant turn over and go back to sleep, its like Ive been asleep for 12 hours straight, I wake up and I have to get out of bed. Its more often that I get 1.5 hrs sleep, well thats from the time I go to bed to the time I wake, so it counts falling asleep too. I often end up falling asleep at the table because it hits me that I am overwhelmingly tired with little warning. Ill feel tired or like Im getting tired and then wham, Im asleep or fighting to stay awake and its too late to get to my bed. Then I do manage to get to bed, I sleep for a bit over an hour and Im awake again, like seriously whats with that. To my mind you cant be so tired that your falling asleep at the table doing something, as Im almost always writing when it happens and get an hour or so sleep before being awake and ready to go again. I have to try and tee things up each day so that Im awake enough for appointments but have time to nap between so I can continue. I cant really blame this on medication though as I was like it, maybe differntly or not as bad before I started the new medications. Ive been on the new psych meds a week, I know they take a while to kick in though its said to be 1-2 weeks for you to start to feel it so I am at the early stages. I can say that my hallucinations and disassociation has been reduced a lot but I am considering making another appointment with the psychiatrist to discuss options surrounding my sleep because there has to be something better than this. I had hoped this medication would help, I think it might have made things a little worse again but not something I havent experienced recently. I just want to go to bed at the same time each day, sleep and wake around the same time and that be the end of my sleep needs. I dont want to need to sleep during the day, to be tired all day, to be watching the clock to work out when it will be acceptable for me to go to bed, though the last has pretty well stopped. At the moment when Im tired enough that I will sleep, I go to bed.
On that note, Im going to bed. Its 2:25am, Ill probably wake up around 4am. But I need some sleep. Im not tired tired, so I may not sleep, Im kinda giving it a go. I am tired, its just that Im not falling asleep where I sit. Im really hoping I get a decent sleep, I must have some hope in me cause I still set my alarm to make sure I go too my appointment on time. Its my first ever podiatry appointment tomorrow, Im not really sure what to expect. My feet arent great, they hurt alot, my heel is pretty horrible but mainly I need my toe nails cut and Im hopeful they do that. After that I have my diabeties educator, thats over the phone, which Im pretty happy about to be honest.