Tuesday 26 February 2008

The last 24 Hours.

Just want to make you all aware of what has happened since the NAM/THT meeting.

You may recall a gentlemen. Who contributed to this meeting last evening. Who seemed to have some specific benefits realted knowledge. I have had some discussions with him. I will check to see if they he doesn't mind me using their first names on here. UPDATE : His name is Steve and he has good background experience.

Steve will be providing some information on the process we might go through when challenging any adverse decision we might have on our reviews. I will post it when I get it. Thanks guys.

They along with many of the comments both last evening and received during the day.

Clearly point to us having to organise ourselves better.

Many have the professional skill sets we need to make a start, and have made them available to help fight the issues we face. Though to move forward will need to find others with appropriate specialist skill to also help.

Time is the enemy of us all so we must seek to use it wisely.

Again pointing to the need to put a structure in place to play to our strengths as a community. Where serving the community as a whole is paramount and “ego” is left at the door.

So the current "background" conversation is around forming a "legally defined" organisation, a charity. So we can fight under the banner of a group rather than individually.Applying for funding for the incidental costs of running a campaign.

Clearly there is a niche for a national organisation to campaign for those within all of our HIV community. Who, for whatever reason. Rely on the state to meet their day-to-day financial needs.
  • To ensure that our community can access clear information for they or there support workers to use to help get those with HIV, the financial assistance they are entitled to.
  • To raise awareness of the issues the HIV+ community faces to ensure fairness from the State in relation to benefits.
  • To utilise the strengths and skills within our community to achieve this.
  • An organisation that remains, independent, politically impartial, where no conflict of interest prevents campaigning on the issues.
  • Deriving funding on the basis it is without strings allowing the voice of our community to be free.
  • That where you live & how your local council invests it money in HIV services, doesn’t dictate who you can approach for support.
  • To partner with likeminded organisations subject to the aforementioned.
  • An organisation open & transparent to those who may use it.
  • Accountable & scrutinised by those who use it.
  • Ideally a co-operative type model where we all hold a stake.
  • Where those who hold the necessary offices of responsibility do so on the basis that stakeholders have clearly indicated their ongoing approval.
  • That our aim should be to accept criticism as a driver towards excellence. Where it is always welcome.
Always moving forward. Thinking out of the box and out of our comfort zone where necessary.
Realising our limitations today are our goals for growth, tomorrow.

Initially this organisation will, because of size, only be able to generally help though the web & other media. Provide general guidance and information.

An organisation that empowers members of our community to tackle the benefit issues they face more specifically and independently. Giving the confidence to do so.

Though its existence & work. Shines a light on the failure of others i.e. the state. Taking them to task where appropriate.

I believe our community fell asleep. Many I meet are “seasoned” campaigners who fought for the rights our community have enjoyed, including myself, since the early days of HIV/AIDS. Many of these have because of age, numerous drug regimes and the results of surviving long term with HIV. Are not able to be as vocal or active of some of us. But we must harness this vast pool of strategic & tactical campaigning experience.

Most of us have Disability Living Allowance because of the fighting these people did at the time.

I have benefitted from this early work. Now it is my turn to stand up and be counted. I am so grateful for the advice, guidance and support.

We were caught of guard. We have some catching up to do. Our campaigning is already showing some results. We can do more.

We must not allow our community to sleep again. We must ensure the “mantle is always” passed on. Under the guidance of those who came before & learnt many of the lessons.

We know the how & why we feel let down over getting help with our benefit problems. Lets right this shameful wrong.

Many people who find this site thank me. Which I appreciate.

What can I do to help? They ask.

Very simple.

  • If you have a view or opinion express it.
  • If you have a criticism, make it.
  • But to serve us all. Spread the word, create awareness.
  • If you only tell one other person that is a tremendous contribution to this cause. Awareness is golden.
These are my views and opinions. Please. I invite your comments.

This should be by us, for us, to serve us.

8 comments:

Anonymous said...

just wanted to say that the new website is great, i was at the meeting on monday and i must applaud all concerned, it raised some very important issues, it was nice to see so many people attending, i particularly like the idea of checking whether we could challenge the legality of the change from a lifetime award to indefinite, at the european courts of human rights, once again thank you for your website and keep up the good work, i went to the kobler clinic and informed the st stephens volunteers of the meeting and some of the very helpful points raised in relation to mobility cars, oral appeals etc, they were very glad when i informed them of your website and said that they would be using it to help keep people informed, keep fighting xx garry

Anonymous said...

Thank you for the update.
I'm really sorry I couldn't make the meeting as I gather it has given you a certain amount more enthusiasim to get us more organised & a boot up the backside to prove that WE are right to right this injustice.
Thank you to you both, John & partner.

Just a thought on an ardent gay rights campainer for most of our gay years who may help champion our cause.

http://www.petertatchell.net/

I know you mention 'NON-POLITICAL' in you BLOG but I'm sure he can put his 'politics' aside & must be aware of & been affected by HIV/AIDS in the years he has been 'fighting' our corner whether you agree with his tactics or not.

He surely has the know how & contacts.

I know I ceratinly will be watching & listening closely & contributing as much as I can.

Andy

John said...

That evening there was a representtive of the Green Party in attendance.

I told him I felt somewhat disappointed that Peter hadn't picked up on the emails I had sent out thus far.

Peter is very near top on my mass emailing group. Though I appreciate he is a very busy man.

I am happy for help or to partner with any political party s long as it doesn't compromise us as an independent entity. That such a partnership is not seen as an endorsement. That any help given is primarily to push the awareness of the DLA & Benefit issues for us and the wider disabled community as a whole.

Thanks,

John.

Anonymous said...

I to have emailed Peter this was my response...

Thanks very much, (my Name) - I received your documentation.

I'll look at it later, as I'm on the campaign trail for the next few days.

Be assured of my sympathy and support.

Best wishes, Peter

Is this a standard response to emails to Mr Tatchel office?

John said...

I haven't received any response. However we must bare in mind that Peter is pursuing a Political Career with the Greens in Oxford. Whereas I know he will lend his support to this. He is currently engaged in the "bigger picture" of which this is only one issue. Personally I think the "bigger picture" is what he should be pursuing.

Time is the enemy of us all. I spoke to the Brian Paddick team also on this.

I don't always agree with Peter but he is an inspiration given his dedication to many causes over the years. Causes which have been of benefit to us all.

Anonymous said...

After the meeing on Mon. I have recieved my reclaim form for DLA. I have also contacted my MP ( Joan Roddock) informing her of this blog/web page's existence. Although the THT speaker was informative on Mon and thank her bfor that I was a bit disappointed that she didn't have any satisfying response when someone suggested that there may have been some complicity in the decisions of the DWP and THT as to regards this review. ANY OPINIONS HERE ARE PURELY PERSONAL.
This makes me a bit reluctant to use THT to help me with the filling in of the form
Having beeen diagnosed for 23 yrs I am finding this whole procedure more than a little depressing and am not sure how I am going to deal with this practically or mentally

John said...

Joan of CND fame. I look forward to your update on the response.

I have passed thanks on to both NAM and, via NAM, to THT. The event was organised by NAM.

It was probably me that raised the question to THT. My interest was how THT was involved with reporting back on the effects of this review to the DCS Advisory board of which they are a member. They are our representatives on the board and clearly we all want to know how equity is being enforced.

THT had a large crowd on Monday on a sensitive issue.It must have been intimidating for the speaker.

If you are fortunate to have access to a THT center that will help you with your forms. They can be quite lengthy. I would suggest some help is better than none.

If it is the DLA556 form. Deal with it as soon as you can. If you go to THT take a photocopy and fill that in with the advisor.

You can then take a few days to review what was written and if you are happy copy the information to the original.

Call your local THT office and ask for help and mention your concerns, they may give you a fuller answer.

Keep us all up to date.

We all have form views based on our experience. Personally I find critical appraisal equally as important as praise.

John said...

I started this thread basically to get feedback on

a) is there a need to set up a wider ranging campaigning group for issues faced by those who live with HIV? I think that HIV education/sexual health & pre-infection is covered extensively elsewhere.

b) if yes, than what would you be looking for from such a group. Forget any previous experiences you may have had elsewhere. Take a fresh sheet of paper approach.

c) Funding. I know a bug bear. How would we fund it?

d) as someone living with hiv are there any other issues you feel need to be highlighted that are presently ignored?


Thanks,

John.