Snout I wasn't patronising you I was challenging your argument with facts.
Yes I know what it's like FOR ME to have had the mh issues I've had all MY life too. But I wouldn't presume that means I know what it's like for someone else, even someone else with OCD, even someone else with contamination OCD. Even mh hcps will say that knowing what it's like FOR YOU doesn't mean you know how it is for others.
Yes millions of people with OCD live relatively normal, functional lives, working full time, raising families etc I've been one of them for most of my life.
But I've also been one of the ALSO millions who AREN'T functioning, aren't able to work. I have engaged with services fully, I've tried numerous medications, therapy, complimentary therapies (meditation, yoga, breathing exercises), online "courses" all sorts. I'm still currently taking about 3 hours to get up the courage just to get out of bed and get a drink, barely managing the very basics of household and personal care (certainly not up to mn daily deep clean standards nowhere near!). I am seeing my cpn this week and yet again I'm going to be pushing (again) for a medication review as this is the worst I've ever been.
"Yes, I would call them a scrounger, too" wow! Your being "one of them" though (and I'm deeply sorry you're in the situation you are) doesn't make that attitude any more acceptable. It may be right for you that doesn't mean it's right for everyone.
Pushing myself too hard is basically what finally tipped the scales for me into having my first breakdown. Although it's not just down to that it was a long time coming.
I was prior to that very much "a coper" I coped with an horrific childhood, chronic ill health (physical), a very stressful first career, a marriage breakdown while living somewhere I had no support network at all, which left me temporarily penniless, on the verge of homelessness with a 2 year old, being a single mum, while being a single mum also variously being a full time employee or a full time student, part time employee & volunteer, then finally involved in a car accident (I was stationery) which left me physically disabled with no car & no support network. At that point my mind just went "nope!" Huge anxiety, hallucinations, manic/agitated behaviour I could not control. Terrifying.
I almost went into full on "jade" mode then but realised I don't owe you my full medical mh history.
I've worked full time for several years since the first breakdown, but after the second I didn't want to repeat the mistake of going back too soon, I didn't intend at all to not work for so long and I miss it loads having worked since I was 16. But I have had physical health worsening, dds own disability being dx which had a profound effect on her plus she's had a few lengthy hospital admissions herself as a result, problems with meds and well here I am. Last year was especially bad.
"You thought that disabled people with progressive illnesses all stay at home and let others pick up the tab?" Absolutely not. I've several friends & family with physical disabilities, some from birth, some progressive. But if someone has a physical disability that is severe enough that they are unable to work then it's absolutely right that they shouldn't be forced to try & possibly harm their health further, and they should have enough money to live on.
"Where are all these jobs that one can get without qualifications or experience yet pay enough for fulltime nursery plus before and after school care for three children?" Good question I'm sure loads of mums would LOVE to know.
Joanmcc posting that link which was already posted and discussed upthread just shows
You haven't rtft
You've not recognised/acknowledged the huge differences between the 2 scenarios.
Op baby steps - but keep making them.