Hi everyone,
I am posting for some advice from fellow sufferers who have attended The Centre for Anxiety Disorders and/or people who have used the OCD Action Advocacy resource before.
This was the reply which I received from Dr David Veale after emailing him:
“Dear Vicky
I am sorry to hear you are suffering from OCD and it is clearly severe.
Your CMHT do have access to our unit if they refer you to me for an assessment by a member of our team and the local PCT authorise the funding. Referral usually needs to come from a consultant or senior member of team like a psychologist treating you.
You may need the help of an advocate from OCD Action (see their website for telephone number) or PALS who can talk you through what you need to do and be persistent with your CMHT in seeking a second opinion. If still no luck I would enlist the help of your MP.
David Veale”
My questions are:
1) I have emailed Jude rather than phoning her as I do not like to speak to people on the telephone (part of my social phobia) how did you contact Jude? I am not expecting an instant reply from her would it be best if I got someone else to phone Jude as I do not know how often Jude would check her emails.
2) I am expecting my CMHT to say that they will not refer me, if so is this something Jude/an advocate could help me with?
3) Are there OCD Advocates based in each town, for example local MIND? Or do you deal with Jude via emails (telephone for most people I would guess)
4) For people who have attended The Centre for Anxiety Disorders did you have to fight your PCT for the funding? I know each PCT is different, I am just wondering. It seems you have to fight for everything these days.
Thanking you in advance for any replies.
Vicky
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