last ditch attempt with my doc

I hope this post is allowed?
Just trying to spread some awareness of what is going on out there

Funny, when you step through the docs door, knowing my circumstances and asks.:.......what can i do for you. A diagnosis and treatment of lyme would be great please!
No chance of that, especially today.
Instead, i found myself on the receiving end of total ignorance.
My lovely, helpful, understanding, compassionate, doctor (not) read me the riot act. Apparently I need to accept the fact that I don't have Lyme Disease, I need to realise that, whatever symptoms i think i have are been amplified by my OCD, they apparently are not as bad as I think they are. The fact that my ELISA result came back negative, proves that i can't possibly have Lyme.
I have now been refused any further help concerning tests, and i should stop dwelling on the notion of Lyme........I have been offered something though; a psychiatric assessment, yep that's right.
Obviously, I stormed out of my surgery, muttering words such as POLITICAL, PROTOCOLS, FUNDING, DUTY OF CARE, ON YOUR CONSCUENCE.

I was told that.......us doctors only have a small amount of funds available, we have protocols put in place that we have to follow, our funds don't cater for this type of thing.
I am now certain that in the UK, our health service is governed solely by money.

You are very fortunate if you find a GP who is willing to break free of the shackles and give you the duty of care all of us deserve.

I'm hoping that those who find themselves wasting so much valuable time trying to convince doctors, and getting no where, STOP. Explore all your options, but don't be hasty, don't be fooled into believing everything.

If your reading any of the posts on this forum, then you have already made positive steps.
Listen to the people who have been there, take the knowledge they share and use it to get better.
I hope that soon, I will be on the road to recovery, and a positive story will follow.

I am thinking of you all.

Thanks for those kind words MEGOSUN,

Regarding herbal Lymester, this is going to be my next step. There is just so much information about Lyme that i must admit, is starting to bog me down somewhat. My family are starting to doubt that i even have the disease, and private is just not an option at the moment.

Im not sure if this will help me, but im going to get myself some Multi Vitamins and Minerals, some omega-3, and some cats claw, which i believe is the same as Samento???? May be method in the madness, im thinking that my immune system needs a boost.

Antibiotic treatment in UK is just not good enough, 30 days treatment, then refusal of any more. I need something thats cost effective, and that promotes my natural defences............more research.

Need to do something fast, these symptoms are getting worse by the week.

Ive never known anything like this, every door i open is a brick wall, its like a real life Matrix. Wheres my Oracle when i need her?