Jump to content

mikv

Registered Users

Change your profile picture
  • Posts

    100
  • Joined

  • Last visited

Posts posted by mikv

  1. what are you self-medicating with?.

    Is your underlying disease chronic Lyme or an equivalent Borrelial disease?

     

    I have a few things going on but my main issue is usually genetic and affects my connective tissue like a cancer so I cant move without hurting myself .

     

    No meds - I used something else in small doses I discovered by chance .

  2. If I were to move elsewhere like England what are the chances those aware of my history here would look up nationwide E records and involve English police / authorities to monitor me if they could not find an address under my name or clinic I had joined with ?

     

    Would this also apply in another region / health board in Scotland ?

  3. This has been my problem even with a diagnosis ( i have a rare disease ) wildly misdiagnosed is that there is no effective treatment here in the UK - or approved methods that help so I've had to resort to my own which they label " self harming " . They do this because its an improvised version of this treatment I need in the US and because Im self taught .I was doing that for almost 20 yrs until my landlord ( mother )grassed me to doc and kicked me out.

     

    Im trying to find somewhere but on DSS theres zit so I've had to resort to lodge before I get any worse and patch myself up in hope my passport comes so I can go to US and in meantime find somewhere in the UK

     

    Thoughts ?

  4. Small Update

     

    Apparently the fact my original solicitor no showed for 4wks ( the one my advocate recommended )has put my appeal against my detainment in jepodary because it will end soon and the compulsary treatment their making an application for will have began. ( the one for 6 months ) My new solicitor will make an application for the tribunal next Thurs but at such late notice there is no gurantees and my evidence ( which I've been told would prob win the case ) would be meaningless...

     

    A Worried Mike :(

  5. Any one tell me how recent a psychiatrist must have seen a patient in order to approve a short-term detention certificate ...?

     

    Short-term detention certificate

     

    (a) When might a short-term detention certificate be granted?A doctor with experience in diagnosing and treating mental disorder(a psychiatrist), who has examined you, may grant a short-term detention certificate where he/she believes it is likely that

     

    No psychiatrist examined me prior to detainment

     

    Dr M (pysch2) saw me briefly as part of the crisis team not as patient

    Dr T (pysch1) who Dr Shi8 ( gp) contacted for approval had not seen as a patient in 5 yrs

    Dr Shi8 had only seen me once as a patient in 5 yrs re physical for Atos

     

    An MHO has a duty under sections 45 and 61 of the Act respectively to interview a patient when short-term detention or an application for a compulsory treatment order is being considered, unless it is impracticable to do so.

    MHO did not engage me at any point till after detainment in an informal manner re compulsory treatment order.

    MHO did not inform me Section 61(2)©(i) of my rights in relation to the application for a compulsory treatment order.

    MHO did not provide me with information on the role of the named person as suits my needs or anything else .

  6.  

    BTW, a Tribunal might take into account (when deciding if you have capacity / suffer from a mental health problem that you have little insight into) things like "I considered changing my nationality to escape being sectioned" - they may decide it isn't an entirely rational response ..........

     

    TBH that was going to be my final resort if all else failed.

    How are you getting on with:

    a) the independent advocacy service, and

    b) The Mental Health Review Tribunal?.

    A ) not good - the Tribunal is a week and the solicitor has still no showed despite advocate recommending him

    B) ^

     

    I had the mho here today and it seems they have decided to put me on compulsary too.

     

    I asked him about getting an interim to have more time as the solicitor still hasnt showed, any thoughts on this ?

     

    Also having a real problem with doc here etc scheduling meetings without informing me in advance so there is no way for me to prepare and have my advocate here as a witness.

     

    mike

  7. Dear mikv,

    I am writing to you about the detection and sub-atomic properties of the Higgs Boson.

     

    I know absolutely nothing about the detection and sub-atomic properties of the Higgs Boson, and couldn't hold a conversation about it nor to (have enough understanding & INSIGHT) have capacity to discuss it in a meaningful way.

     

    Yet I can write to you about it.

    I can write the same again, without increasing my capacity.

     

    The fact that I can write twice (or more!) doesn't affect if I have capacity or not.

     

    Similarly, you writing twice to your GP doesn't demonstrate capacity on its own : it is what you wrote that will matter.

     

    It's a good thing I have evidence then ; )

     

    You've also asked about a change in citizenship:

    A) you've already noted that you won't be able to change citizenship easily if there is suggestion you aren't of sound mind

    B) if you were a citizen of a different country it wouldn't stop your detention under mental health legislation (though those detaining you would be prudent to advise the embassy / consulate of your country of citizenship, so they can provide you with consular assistance - they might even decide between them it was in your interests to be transferred to a mental health facility in the country of your citizenship, for example)

     

    When you say sound of mind I assume you mean capacity ?

     

    thanks again,

     

    m

  8. The fact that you have been found to lack capacity on the subject of your admission for treatment does not mean that you have no right to be involved in other decisions once you have been admitted. http://bma.org.uk/practical-support-at-work/ethics/mental-capacity/mental-capacity-scotland

     

    How could I lack capacity on the subject of my admission if I wrote to my GP X2 about it ?

     

    He obviously understood me because he replied - as did the cpn on the phone

  9. Heres the whole lead up to how my GP abused my trust and continually lead me into beliving I wasn't at risk.

     

    The whole time I corresponded with my GP he never once mentioned or asked anything to lead me to suspect my mental well being was being questioned( if he had i would have risked

    travel in order to get better) Although i knew there was a good chance he might assume

    i was at risk after he read my history ( which is why I tried to dissuade him) I didn't

    get any hint it bothered him either which you can see from letter he sent me on nov14

    saying he was happy to leave things( despite having 4 - 5 months in which to read my

    history )

     

    After I had seen Crisis resolution team he sent out in SWAT force as though I were

    terrorist I agreed to see the CPN until I found out it was Dr xxx himself who arranged it. Naturally as I had no idea what was going I wanted to find out why so I wrote. His response as it had been before was to say everything would remain as it was. ( Something interpted as meaning prior to subsequent events ) although now on reflection I realise could have of meant the opposite too.

     

    It wasn't long after this and what I assumed had been resolved I received another

    unannounced visit from the CPN and once again I was left confused given what my GP had said. I phoned Mr xxx 2 wks later after sending a fax to my GP and informed him that I had told my GP I did not require his services.When I did not recieve any word from either or a visit from the mho ( as required by law for detainment ) I assumed matters were finally settled only ( without any prior warning ) to be detained .

  10. If I was to change my citzenship how would it effect my detainment ?

     

    https://www.gov.uk/renounce-british-nationality/overview

    When you can give up your citizenship

     

    You can only give up your British citizenship or status if either of the following apply:

     

    • you already have another citizenship or nationality
    • you’re going to get another citizenship or nationality after giving up your British citizenship or status

    You must also be:

     

    • aged 18 or over (unless you’re under 18 and married)
    • of sound mind (unless it’s decided that it’s in your best interest)

     

     

    Can I leave hospital to receive treatment / therapy nearby?

     

    m

  11. If your psychiatric condition may be caused by the autonomic dysfunction of EDS : I'd push for a referral to one of the UK's EDS specialist centres.

    You can always remind the psychiatrists (and then the Tribunal!) "are you sure you have excluded organic disease such as EDS with autonomic dysfunction"?

     

    Yes, see here pg26

     

    There is so little research into eds - mental illness , but the few are interesting

     

    http://www.ncbi.nlm.nih.gov/pubmed/25459977

     

     

    http://bjp.rcpsych.org/content/200/6/508

     

    " Differences in brain structure were not due to overt psychopathology (the hypermobile group only trended toward higher anxiety scores) or basal physiology (no difference was observed in cardiovascular measures at rest). "

     

    " Limitations to our study include the use of a non-clinical sample; interestingly, neuroimaging studies of clinical anxiety groups rarely report enlarged amygdala, suggesting that hypermobility is a distinct phenotype or that amygdala enlargement might be protective in our non-clinical group. "

     

    mike

  12. What is your psychiatric diagnosis?
    delusional..about my illness

    & can EDS present as such?

    why not ?

    don't all people with misdagnosed invisible / rare illness feel strongly about something that is so widely abused & neglected?

    The average EDS can take 10yrs or more and multiple docs so doesn't that persistance indicate a firm belief - that until diagnosed - could be considered delusional too ?

     

    You note "There are no tests available to confirm the diagnosis or distinguish between hypermobile EDS and joint hypermobility syndrome" but that doesn't mean :"EDS and your psychiatric condition can't be differentiated" - they may or may not be distinguishable.

     

    True, but if that firm belief is shared by a leading expert on EDS and the mayo clinic doesnt it change things ?

    Have you spoken to Ehlers-Danlos Support UK?

    http://www.ehlers-danlos.org

     

    No, just the HMSA

     

    If your psychiatric condition has never been associated with EDS you may struggle to show that you don't have both separately.

    Even if I did does my " conditio " really require this ?

     

    12 yr interval since last admission does not fit atypical pattern of the mentally ill ( esp if I am such a risk having travelled to peru / usa,used needles etc )While the last 5 I have been housebound alone with no pysch aid at all so why is it I am suddenly at risk now,when there has been no prior evidence and in fact the opposite ( use of kneewalker as aid instead of scooter before I detriorated ) ?

     

    Were you advised of "the availability of independent advocacy services under section 259 of this Act", and have you contacted them / asked for them to be contacted?

     

    yup

     

    mike

  13. I have been detained under section 44 with what I believe is ehlers-danlos-syndrome and wrongly being interpted as mental illness- they want to do tests but the problem is there is no one in Scotland really ualified to diagnose it . I am already physically much worse which in turn is being interpted as yet more mental issues and can barely type or talk to communicate as well.

     

    From http://www.nhs.uk/conditions/ehlers-danlos-syndrome/Pages/Introduction.aspx

    There are no tests available to confirm the diagnosis or distinguish between hypermobile EDS and joint hypermobility syndrome. The diagnosis is made based on a physical examination and a person's medical history.

     

    https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/260562/UK_Strategy_for_Rare_

     

    Rare diseases are covered in

    undergraduate and postgraduate medical

    training in the UK. But it is unrealistic to

    expect primary care staff such as GPs (who

    are very often the first point of contact) to

    recognise all rare diseases. Many diseases

    are so rare that a GP is unlikely to see a

    single case in their whole career. Timely and

    accurate referral is therefore a crucial skill

     

    Can any one tell me what criteria allows drs with no previous -or very little to fairly assess a rare disease with high rate of misdiagnosis instead of allowing them to get referred or go pvt ? ( esp in the highlands were there is 0)

     

    If its possible for someone detained under section 44 to seek help privately for assessment if the resources req to rule out a condition are unvailable in scotland esp if there is proof /

    reason to doubt a mental illness ?

     

    thanks

     

    mike

  14. Your description of a sudden visit by 3 people like that 'on medical' grounds sounds to me very much like what happens in England when someone is 'sectioned' under our Mental Health Act 1983. Happened to my sister. Usually this is, initially, for 'assessment' under section 2, and basically comes into operation when a doctor considers that a patient might be at risk of harm to himself\herself or to others.

     

    That Act largely doesn't apply in Scotland but the one summarised here does:-

     

    http://en.wikipedia.org/wiki/Mental_Health_(Care_and_Treatment)_(Scotland)_Act_2003

     

    I am not at all familar with the statute, but, looking just at the summary, it might be the case that your GP issued an 'emergency certificate' with the intention not so much of detaining you but persuading you to accept more assistance from professionals. Pure guesswork on my part, but it's a theory. I would go ask the GP.

     

    Yes , I agree .

     

    I was sectioned once but that was 11 yrs ago due negligence of my illness ( Ehlers Danlos Syndrome ) and they're trying to do it again it seems because my family has complained to them ( they are in denial of it )

  15. I had 3 medical people unlawfully enter my home today ( they walked right in )

    without being notified or informed in advance by any of them or my GP . From what I understand they believed I am at some risk ( without being able to tell me why ) other than my GP's concern over my well being. ( again another mystery )

     

    I requested they leave - they did not and questioned me despite my inability to speak without a struggle / pain ( something my GP knew ) and then gave me ultimatum which boiled down to being forced to see a social worker ( which I assumes means I am now detained )

     

    I still have no idea of how this suddenly happened , but I am not happy about it one bit.

     

    Can any one suggest what my rights are in regard to this , and what I should do ( I'm in scotland )

     

    thanks,

     

    mikv

  16. It's up to you what you spend your money on. Why not pay your Mother for the care she gives? Then it's up to her what she does with her income. Who knows, she might choose to save it up to go towards the cost of a relative's trip to America ...

     

    I intend too she had been helping since 07 , but she was told her pension rules her out of carers allowance because her pension is over £60.00 a week.

     

    mike

  17. Thanks everyone for your replies.

     

    As far as the op in the US ( never mind consultation , xrays etc ) I would probably be looking at something that costs far more than 16,000.00 and prob closer to 100 at least .

     

    And the only way I could even close to ever getting that was if I had some property I could perhaps rent such as this flat - which of course would mean I'd lose benefits which in nutshell is the dilemma of being expected

    to live on under 6 grand - or even 16 grand.

     

    There are other treatments ( some less expensive ), but they are not proven or that cheap ( like stem cells ) or more experimental things which would prob be more temporary and require multiple / yearly returns .

     

    Mike

×
×
  • Create New...