Quin's Adventures

Rants, ramblings, and random stuff from the mind of Quinton "Quin" Reeves.

Monday, December 07, 2009

Blood Frontier "Beta 2" Out Now!

EmblemAfter many months of development, and massive amounts of input from the public, we are proud to present you with the new release of Blood Frontier, v0.85 (Beta 2). This new version totally redefines and improves the game in many ways, creating a whole new style that makes it almost nothing like its predecessor.

We hope that you enjoy this new release, which contains more bug fixes, feature additions, and improvements, than I could ever list. The previous "Beta 1" package saw us gain a huge increase in contributors and players, which has in turn afforded us more resources to create a better polished Blood Frontier.

Video effects courtesy of Animoto: The end of all slideshows! Blood Frontier was kindly given an all access pass during their "Animoto for a Cause" promotion; thanks guys!



New improvements include:

  • Enhancements to the impulsing (double jump) system; sprint for more speed, run along walls, or kick off them.

  • Fun new secondary fire modes for all weapons; stick grenades to walls, or liquefy your enemies with a big blue ball of death.

  • New and improved maps from the community; enjoy a wider range of playing environments and settings.

  • Refined and increased HUD visibility; always know what's happening and what you're looking at.

  • More variables than ever; tailor gameplay to your tastes with more options than you could ever play with.

  • Story mode concept; take the precursor to coop campaigns out for a spin with bots or online.

  • Refinements and polish; gameplay flows easier, visual elements look better.


Special thanks go out to those who enjoyed the game enough to come and offer their help, you should all know that it is very much appreciated; without the advice and opinions you offer, Blood Frontier would not be nearly half as polished as it feels now. Be sure to pop by our chat and leave your own feedback!

Don't forget to spread the word, invite your friends, have fun, and maybe even donate a little to help us keep the project going. Without you we would not exist today.

Blood Frontier, It's Bloody Fun!

Download, Learn More, or Get Help today.

Thursday, April 30, 2009

A Road That Never Ends

Another appointment today, more tests scheduled. Dr Rahman is however persisting in finding out the cause of my problems, despite the fuss I've kicked up. Apparently, I have a gene from one parent that can cause inflammation, but as it isn't from both parents so there's only about a 1-6 percent chance that it can cause any symptoms, he's said he can't give any real answers there. MRI showed a buildup of fluid in the hips, the right side moreso than the left which is consistent with the amount of pain that I suffer, Bone Scan revealed nothing of interest. He now wants to run a test on the fluid in my hips, to identify what it is; which means sticking a needle in there and draining it out - not something I'm looking forward to, but at this point I'll do anything to get some real results. He's given me some anti-inflammatory medication to help with the symptoms, which I'm most happy to try and I do hope it gives me some relief.

Of interest, he did mention that the hospital administration made him aware of this blog, and told me that most doctor's would have had nothing to do with me after this point (where I created alot of trouble), but that he has continued to work on the case because he thinks that I am just frustrated, which I am; ten years is a long time to wait for a diagnosis. He mentioned the word "public domain" alot, I am assuming he meant that the things I have written could be considered defamation of character. I assured him that most of it was not personal, this is just a place where I write down my life and share it with people so they can better understand me and the problems I face. To be honest, he's done very well to continue on with his job despite the complaints, and he has done more to find answers than any doctor ever has; which overall makes me pleased with his efforts.

This doesn't however mean the ordeal is over, far from it. Until I get a diagnosis there is still a wide range of problems that I suffer as a result of my illness, most of them being financial (Centrelink) related. My main point is that awareness about the shortcomings and underfunding of the public health system should be made, and that steps to fix it need to happen. I've gotten responses from the Federal and State members of parliament now who have told me that they will look at the situation; I don't know at this point if this is just an attempt placate me or a serious attempt to fix the problems I face. As usual, only time will tell, but one must keep up hope.

Thursday, April 23, 2009

Linux Lunacy

Okay, so since I got my brand new PC, I've had a few spare parts to play with. I went to rebuild a system with some odds and ends using my previous board, only to have it mysteriously shut down and start screaming this high pitched noise. Further investigation (read; pulled the entire sucker apart until it was nothing) showed the CPU became unseated from its socket. I assume heat did it, because none of the clamps had come off and the heatsink was firmly attached. Unfortunately, the CPU is fried, so I dug out an even more ancient board, my old AMD K7 with a Duron 850MHz.

After messing around a little, I finally settled on using Debian; I was looking to set up a media center in the lounge room for my mother to watch videos on (as she's using her ASUS Eee-PC with its tiny screen at the moment), but I also wanted a system I could (ab)use remotely - Linux seemed to fit the trick nicely - or so I thought.

I have literally spent the last three days, two migraines, and generally making myself feel crappier than I am - not really over installing Debian itself, the whole process of putting a base system on there went flawlessly after I realised GRUB's "Error 18" meant the board's BIOS couldn't handle a boot partition of more than 8GB. I guess the board really is old, and to be honest I am surprised it still works, it's been collecting dust for over six years now. My problem lay in trying to get the 3D accelerator (an ATI Radeon 9550) going, which was orphaned by the dead system.

Now, I'm no Linux newbie, I've used it quite competently in the past (to the point where I even had fun playing with Gentoo at one stage), but the error I was getting had me stumped, X.org would boot, but all I would get is this:
(**) fglrx(0): using built in AGPGART module: no
(II) fglrx(0): [pci] find AGP GART
(EE) fglrx(0): [agp] Failed to get AGP mode!
(EE) fglrx(0): cannot init AGP
(II) fglrx(0): driver needs X.org 7.1.x.y with x.y >= 0.0
(WW) fglrx(0): could not detect X server version (query_status=-1)
(EE) fglrx(0): atiddxDriScreenInit failed, GPS not been initialized.
(WW) fglrx(0): ***********************************************
(WW) fglrx(0): * DRI initialization failed! *
(WW) fglrx(0): * (maybe driver kernel module missing or bad) *
(WW) fglrx(0): * 2D acceleraton available (MMIO) *
(WW) fglrx(0): * no 3D acceleration available *
(WW) fglrx(0): ********************************************* *

No amount of messing around with the Proprietary or Open Source drivers would do anything to fix this, something was stopping it from getting access to the AGP card. My friend, Hirato, even decided to give it a shot by logging in remotely and playing around (I suspect to stop me from getting dismayed at Linux completely), but even he gave up after a few hours, it seemed unfixable. Even Google was coming up pretty useless here, and us geeks basically use it as our #1 information resource on the internet. Most people were having the exact same problem, but there was never any real solution from others, and I guess anyone experiencing the problem either gave up or never posted their success story; so that's what I'm trying to do here now to fix that.

So, I was about to give up, as my headache was starting to return from overexertion, when I decided to whack one more last-ditch search into Google: "linux agp amd k7". The results themselves didn't look too promising, apart from the top two which were mailing list threads (on an almost completely irrelevant subject), but I decided to flip through the threads nevertheless. There was a bunch of talk about kernel crap and debug calls, but the end result of those discussions ended in one clear thing; EDAC on an AMD K7 running Linux steals system resources and doesn't release them to other modules, like "agpgart".

To me, it seemed a bit far fetched, but I decided to give it a go anyway - I had nothing left to lose. I ran a "lsmod | grep edac", two results; "amd76x_edac" and "edac_core". Okay, so I poked around /etc a little and found "/etc/modprobe.d/blacklist" to the bottom of which I placed these two lines:
blacklist amd76x_edac
blacklist edac_core

I then rebooted the machine just to be sure everything was back to running how it should be, as I had been messing around alot, but I'm pretty sure I could've just run "rmmod" on the modules if things had have been clean. To my surprise, I ran "startx" and the damn thing worked.
(II) fglrx(0): AGP card detected
(**) fglrx(0): using built in AGPGART module: no
(II) fglrx(0): [pci] find AGP GART
(II) fglrx(0): [agp] AGP protocol is enabled for graphics board. (cmd=0x0f000314)
(II) fglrx(0): [agp] graphics chipset has AGP v2.0
(II) fglrx(0): DRI initialization successfull!
(II) fglrx(0): Acceleration enabled

Honestly, I did a dance in the living room right then and there. Three days of messing around and it was something as simple as removing a couple of faulty modules, I really couldn't believe it. It's this type of obscure annoyance that made me give up on Linux in the first place, but I really have to say I am overjoyed to have found the solution which nobody else could seem to correlate. So if you're having trouble getting an AGP card going in an old system (namely the K7 series motherboards), try turfing out the "edac" modules - it worked for me.

And that's my success story on another adventure in Linux Lunacy, hopefully you Google'rs will come across this entry in the years to come, find it answers your question and be forever grateful that you never got the headache I had to endure. Happy 3D acceleration to you.

The Power of Persistence

Following a letter to my Local Parliamentary Member, Jon Sullivan MP, he forwarded my case on to my Federal Member, Peter Slipper MP - who seems to be pursuing the case, to which I could not be happier. It is finally looking like that my persistence is paying off.

Jon Sullivan MP, Federal Member for Longman
12th April 2009

Hello Quinton,

I have had a quick review of the material enclosed in this email, which
I will forward to your Federal MP, Peter Slipper, for his information,
as it is not appropriate for me to act on behalf of another MP's
constituent.

For what it is worth, were you my constituent I would strongly advise
that you take the advice to visit a GP so that issues relating to your
entitlement or otherwise for a Disability Support Pension can be
resolved.

Issues relating to the HQCC are matters for your State MP, Andrew Powell
who I understand can be contacted on 5495 2666.

Jon Sullivan MP
Federal Member - LONGMAN

Okay, so he wasn't all that sympathetic, but he forwarded it on nevertheless.

Peter Slipper MP, Federal Member for Fisher, via Michelle Ellis
23rd April 2009

Dear Mr Reeves,

As advised by the Member for Longman, your correspondence has been forwarded to me as your Federal Member.

My staff have tried to communicate with you by telephone however I understand your home and mobile telephones are unable to receive incoming calls.

It is my understanding that you have not applied for a Disability Support Pension and/or Mobility at this stage and you are currently in receipt of Newstart Allowance.

I understand that you have also communicated with the Chief Executive Office of Centrelink concerning this issue.

As requested in your correspondence I have made representations to the Parliamentary Secretary for Disabilities and Children's Services and when I am in receipt of a response I shall again contact you.

Kind regards
Yours faithfully

Peter Slipper

That looks a little better, doesn't it?

Quinton Reeves
23rd April 2009

Dear Madam,

Thank you for forwarding this correspondence from Peter Slipper, dated April 23rd 2009.

I can confirm that I have not yet applied for Disability or Mobility Allowance due to the fact that the officers at Centrelink continually refuse such requests on the basis that my illness is not yet diagnoses (a process which is ongoing and could take a considerable amount of time). However, there is a great strain on my income as my condition has worsened; I am unable to claim compensation for my travel expenses, and the rate of payment on Newstart Allowance (Incapacitated) is considerably lower than that which I would receive on Disability Support Pension w/ Mobility Allowance. This has severely limited the amount and type of help I can seek from medical practioners, further hindering the progress of my case.

Despite the inability to prove my illness thus far under the Social Security laws; I am still, nonetheless, suffering both physically and financially under a system which is unable to make allowances for exceptional circumstances such as mine. It could be years before I am properly diagnoses, and until then a doctor will not sign off on a legally binding document required by Centrelink, for fear of litigation and malpractice.

I appreciate the involvement of your department, and hope toward a positive outcome. If I can help in any way in this matter, please do not hesitate to continue contacting my by email, which is my most reliable form of communication.

Sincerely,
Quinton Reeves

Thursday, April 09, 2009

Proof Positive

Finally, there's progress! "Clinical anomalies" have been identified in my tests which should hopefully lead to some answers.

Tammy Salomon, Patient Liaison Coordinator, Caboolture Hospital
9th April 2009
Dear Mr Reeves

I have been informed that your MRI and blood results have been reviewed and some clinical anomalies have been identified. The results certainly validate your ongoing pain issues. Dr Rahman is eager for you to have a bone scan and further blood tests to assist in providing a definitive diagnosis, and in directing the best course of treatment to provide you with the best possible outcome.

I have taken the liberty of booking the bone scan for you which is scheduled for next Friday 17th April at 8.30am. When you arrive at Medical Imaging you will have an injection and they may undertake a scan or x-ray following this. You will then need to wait for 2 hours for the injection to uptake followed by your bone scan. You can eat, drink and take medications as normal prior to the scan.

We would also like you to have further blood tests. I have placed the pathology request form in an envelope at the front counter of Specialist Outpatients and was hoping you may be able to collect these when you come next Friday.

Please do not hesitate to contact me if I can be of further assistance.

Kind regards
Tammy Salomon
All original content is (C) 2006-2009 Quinton Reeves
Use without express written permission is strictly prohibited.