ASD diagnosis for women

Hi everyone! 

I'm new here as of today. I'd like to introduce myself and a bit about why I'm here and I'm interested in speaking to anyone who can offer me any advice or insight into the ASD condition and diagnosis process, especially from the perspective of a woman.

I'm now 28 years old, and a couple of years ago after researching a lot about ASD symptoms in women, I felt a lot of them rang true with me and experiences I have had in my life. By no means do I think I am a severe sufferer, but my life is definitely shaped by the difficulties experienced by members of the ASD community. I am certain of this.

I was so certain I took myself to a local autism group and met some members so I could speak to them about their experiences with autism. There was one guy there I could relate to. He worked as a graphic designer (same as me) and experienced similar difficulties as I had. However all the members of the group were male and were experiencing symptoms which were a lot more noticeable and severe than my own. I didn't feel like this was what I behaved like, and so I wasn't sure if this could be the condition I have.

After a long wait I eventually got to see a psychiatrist whose job it was to screen me for ASD symptoms before referring me to a specialist to take an official test. She was more interested in speaking to my Dad and asking him some questions about my developmental years. My Dad said I acted normal for a child, however I was very shy, which I still am today. From this account, she decided not to refer me to see an ASD specialist. I was so distraught when she told me this I couldn't actually move or say anything. I know I have this condition, but my behaviour is not as noticeable as a males, and I was not being allowed to even be tested for it because of this.

I had just quit my job as I was having real problems working in an open plan office, and the psychiatrist said I was suffering with an anxiety disorder, and so referred me to see an occupational therapist to help me deal with working environments. I saw the occupational therapist for a while but she had nothing helpful to offer me as I am able to work, but not in an open plan office surrounded by people. And that's nothing she could change.

The occupational therapist then referred me to group counselling to help me with expressing my emotions with groups of people, and I am now in the middle of this treatment.

The one thing the group counselling has shown me, is it same difficulties I have with relating with groups of people which are all ASD symptoms. I am back where I started two years ago believing my problems are caused by an autism disorder and I don't know where to go from here. I have considered going back to the GP and asking to see the psychiatrist again, but the experience was so stressful and I had to do it all on my own, that I am not keen to have to state my case all over again.

Have any women on this forum had an experience similar to this in their journey to diagnosis? I don't think I behave in an obviously autistic way at all. I think in fact I am very low down the spectrum if I do have ASD, but I have experienced break downs and had to quit jobs because of my symptoms, so I feel like I need to complete an official assessment in order to find out why I am like this. However I don't know how I can do that if I can't even get past the screening stage to see an ASD specialist.

If anyone has any advice or insight into how I can move forward, I would be really really grateful. Thanks

Parents
  • I had a similar experience in that a lot of people (one GP and several mental health professionals) said variations on the theme of ‘don’t be silly, you’re a girl and you can make eye contact’ to me over the three years after I first raised the possibility. It took me having a complete breakdown, snapping and going private and seeing a clinical psychologist that actually knew what they were talking about to get a referral. 

    In the end I went private for my ASD diagnosis due to not wanting to wait another two years, but strangely at that point everyone else (a new GP, another psychiatric nurse, aCBT counsellor) all independently also acknowledged that I was probably autistic . I dont know if that means that over time, knowledge of the differences in women and men with ASD are gradually becoming more known, or whether I was just more confident in approaching them by then. Either way my psychologists advice to me was to ‘whatever you do make sure that where you go for a diagnosis is used to diagnosing women’  I think that is probabl6 very good advice if you hav3 any choice over where to get a diagnosis.

    I would also recommend clueing yourself up about ASD in women as much as possible. The NAS women and girls training module was very very useful to me. Not sure if it’s still free but worth it if it is. At some point I started realising that I knew more about it than many of the people who had initially said no way to me. If you think you do have ASD have confidence that it’s worth getting a proper diagnosis i’d Say

    Good luck :o)

  • Hi Zomted, Thanks for sharing your experience with me.

    I wonder if you need to approach the GP more than once for them to take you seriously? It seems that way. That's great that you managed to get a diagnosis eventually though. 

    Did you get offered any help or advice on how to manage your symptoms after your diagnosis?

Reply
  • Hi Zomted, Thanks for sharing your experience with me.

    I wonder if you need to approach the GP more than once for them to take you seriously? It seems that way. That's great that you managed to get a diagnosis eventually though. 

    Did you get offered any help or advice on how to manage your symptoms after your diagnosis?

Children
  • There’s a support group available, but apart from that not really. For me though I’ve found it incredibly useful to meet other autistic adults. Also I’ve done a lot of my own research which has been a revelation. Suddenly everything is starting to make sense and I accept myself as I am, which I never did before. The most important thing for me though has been that telling work has meant I’ve bedn able to access adjustments ( eg flexible working) which have made a huge difference to me.