Hell to help Olivia.

one does not promote charity, for personal gain.

It happens a thousand times a day in a thousand different companies.

"1$ from every purchase goes to 'Save the Lemmings Foundation' " etc....

There are ads on all the time from one company or another saying how much they donated to this or that charity even after they have stopped collecting for that particular charity.

The perception of a social conscience creates 'warm fuzzies' and 'warm fuzzies' translate to more dollars.

This comes back to the philosophical debate of whether true altruism is actually possible.

All I can say is if it was me looking for 'one more chance' at something like a normal life I may not have such high standards about who got the 'fame' for raising it.
I'd like to think there would be limits of course.
There would certainly be some people or organisations I would rather say "Stick your money,I'll get it another way" and it's easy to say what you think you would do in such a situation but till you are in that situation and staring down the barrel of that gun you can never truly know.
 
It happens a thousand times a day in a thousand different companies.

"1$ from every purchase goes to 'Save the Lemmings Foundation' " etc....

There are ads on all the time from one company or another saying how much they donated to this or that charity even after they have stopped collecting for that particular charity.

The perception of a social conscience creates 'warm fuzzies' and 'warm fuzzies' translate to more dollars.

This comes back to the philosophical debate of whether true altruism is actually possible.

All I can say is if it was me looking for 'one more chance' at something like a normal life I may not have such high standards about who got the 'fame' for raising it.
I'd like to think there would be limits of course.
There would certainly be some people or organisations I would rather say "Stick your money,I'll get it another way" and it's easy to say what you think you would do in such a situation but till you are in that situation and staring down the barrel of that gun you can never truly know.
You forgot this is NEVERDIE, so when he does it, it's deplorable. When others do it, it's commendable...:rolleyes:

That's the message people are sending, anyway.
 
...Mindark the developer of the Entropia Universe platform will oversee the distribution of funds....

Copied from http://www.gamasutra.com/view/pressreleases/72464/ROCKTROPIA_Virtual_World_Aims_to_Make_the_Devil_Pay_to_HealReality.php

:duh: I was all gung-ho to participate until I read this part. Oh yeah they'll "oversee" it all right...and gladly skim some off the top for the service. Literally turns my stomach to think MA will be getting their greedy hands on this well-intended money. I'll donate directly thankyouverymuch.
 
So it's not charity.

Its promotional.



Cmon Neverdie, chip in 5% as well as the 5% tax THEN call it charity!
 
So it's not charity.

Its promotional.



Cmon Neverdie, chip in 5% as well as the 5% tax THEN call it charity!

my point exactly, or make it 2.5% each :wtg:
 
No we don't own a house. Obviously would have sold any assets for this if we had em. The reason few scars could answer the question is because we are good friends and knows our situation.

Thanks for a response, as it certainly isn't obvious to the public whether ot not you've sold any personal assets (RL or ingame) to attempt to pay for operation number two.

Just today alone, you bumped seven sales threads of items valuing (with your asking MU) TT+11K peds ($1,100US). I think that if you reduced your prices a bit and unloaded all of that stuff (including other equipment and any skills on your and Erica's avatars) you could make a significant dent in your expenses for Erica's second operation.

I won't speculate on how many peds you have tied up ingame, because that's not obvious.
 
The Liberation Treatment: A whole new approach to MS - CTV News

One of my 2 sisters and I have this horrible disease. The treatment works, but the clinic I went to did not use balloons that were large enough, and so I restenosed (the veins snapped back to original size and shape.
The condition i9s called CCSVI (Chronic Cerebro-Spinal Insufficiency).

Contact me on Facebook for more info if you like. Olivia LivForever . :)

The video is very interesting. If all this is for real then my best wishes to you and I hope you can raise all the money you need for the treatment. If it is all a scam then shame on whoever is responsible.

I don't care too much about your ingame reputation (haven't even read about it) because I know how the popularity works in this forum, so you might just be the victim of one of the many witch burning seasons in here.

As for ND using this as a PR stunt, well he might be but he also is giving people the oportunity to donate to a person in need thru a recognizable company, so it's less worysome than when individual avatars create charity funds. I also agree he should have offered to put as much money from his own pocket as it was collected from taxes.

I am also convinced that if tomorrow the news announced that one Jon Neverdie Jacobs discovered the cure to all forms of cancer and gave it freely to the UN, some people in this forum will come and critizice him for not discovering it 20 years ago and preventing so many people from dying. You know who yo are :silly2:.
 
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I think for all of neverdies flaws he's not really the one to go after on this topic.

Of course it would be really nice if he chipped in money himself for this aswell, BUT, he actually helps to facilitate for a possible good outcome for Liv and her family and friends.

If this promotion or whatever you want to call it didnt happend, the chances for Liv to actually get $15 000 in donations to pay for her operation would be alot slimmer.


For Liv and ND this is a win-win situation as they both benefit from it, altho how much ND should win/profit from the situation seem to be whats up for debate. I think we should let the guy off the hook this time, well atleast until he's in the press saying how he paid for her operation when in fact it was entropia players. But time will tell...
 
Doesn't hurt to be a bit paranoic when it comes to anything in the internet. For me personally anything that is somehow related to Carlito Carl Brigante is dubious until proven otherwise anyway.

I completely agree.
 
Thanks for a response, as it certainly isn't obvious to the public whether ot not you've sold any personal assets (RL or ingame) to attempt to pay for operation number two.

Just today alone, you bumped seven sales threads of items valuing (with your asking MU) TT+11K peds ($1,100US). I think that if you reduced your prices a bit and unloaded all of that stuff (including other equipment and any skills on your and Erica's avatars) you could make a significant dent in your expenses for Erica's second operation.

I won't speculate on how many peds you have tied up ingame, because that's not obvious.


Yes those are the last of my few valuable items I have here. But due to downturn in game lately, the luxury type items don't sell like they used too. Also avatar skills wise don't have much since have chipped out several times in last few years to keep playing. But for anyone else and to put this to rest, we are in process of selling out all skills and assets to gather what we can for the procedure.
 
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I find it mildly amusing that you can answer a question about account values with such authority when it wasn't even directed at you.


Maybe Erica will actually answer.

Also, still waiting for an answer about a house... :wise:

Hi Chrome. I am just checking this thread for the first time since I wrote my many replies the other night; it took everything out of me as I was barely able to raise my arms to my keyboard (and my fingers were partially numb.)

Today is cooler and perhaps not as humid (?) so I am able to reply here.

Few Scars is correct; we have very little of value left in Entropia - save for a number of great friendships that have develped over the past five years or so...

Carl and I each had a shop in Omegaton West Habitat on Calypso. Both have since been sold. I had an apartment in Omegaton also which we sold.
We love rare Entropian furniture, clothing and art. We've collected many beautiful pieces over the years, and have sold all but a few.

Our soul focus now, is to sell many skills and items to add cash to my Liberation fund.

I have had the fortune to experience different professions, from Beautician and Colorer, to Hunter and Miner. You can ask Carl or any of my friends in-game - I spend most of my time chatting with friends in Entropia that anything else! I've reached level 38 in the Chatter-box' profession!

We are not the type to ask others to support a fundraiser NEVERDIE so graciously, and surprisingly started to help me get treated in California for CCSVI/MS - and not contribute to my own fund in any way we can.
We will still continue playing the game we love, we will simply start over at 'noob' level! :wtg:
Back to sweating and the odd Opallo Team hunt for Liv & Carl (and my favourite, CHATTING!!!) :broke::sweat: :handgun::grouphug:
 
It is sad when humanity turns its back on those in need. I agree everyone in this game is trying to make a profit, get a better MU, but this is not the case here. This is not a hoax, it is real and Erica will suffer greatly if she doesn't get the treatment. If it doesnt work, well at least she gave it a shot!
People bag Carlito for trying to sell Pixie SGA at high MU, so what, does it really matter what MU he sets? Not at all. At the end of the day, if no body buys it, then that's simply that. This is just a game people from all over the world play for a break from reality.
I feel that Erica and Carl are decent people who have lost everything secondary to a major illness. They have never asked for anything, just selling everything they own. Neverdie out of some random act of kindness gets Ericas number and calls her and offers Taxes from hell. Good for him.

I will also step up now. My contribution to your treatment will be $250 USD. It's not much but a start. I will not do this via EU as the deposit fees and international transaction fees will eat up precious dollars. I will PM you Erica to sort out a PayPal transfer.

Good luck
Your friend
Bjorn/Few Scars
 
It is sad when humanity turns its back on those in need. I agree everyone in this game is trying to make a profit, get a better MU, but this is not the case here. This is not a hoax, it is real and Erica will suffer greatly if she doesn't get the treatment. If it doesnt work, well at least she gave it a shot!
People bag Carlito for trying to sell Pixie SGA at high MU, so what, does it really matter what MU he sets? Not at all. At the end of the day, if no body buys it, then that's simply that. This is just a game people from all over the world play for a break from reality.
I feel that Erica and Carl are decent people who have lost everything secondary to a major illness. They have never asked for anything, just selling everything they own. Neverdie out of some random act of kindness gets Ericas number and calls her and offers Taxes from hell. Good for him.

I will also step up now. My contribution to your treatment will be $250 USD. It's not much but a start. I will not do this via EU as the deposit fees and international transaction fees will eat up precious dollars. I will PM you Erica to sort out a PayPal transfer.

Good luck
Your friend
Bjorn/Few Scars

Thank you SO MUCH! An old friend of mine who is a web designer, payed for the domain name and made this site... Operation for Erica .

The PayPal Donate button is at the bottom of the page. :)
 
I did some reading about MS and CCSVI. It's unclear at this point if CCSVI is causally linked to MS...
Also, no 100% evidence that the proposed investigational procedure will be successful.

Here is the link to articles related to CCSVI in pubmed...... there are 48 in total

The key word here is "Investigational" it may or may not work..... but someone has to go through this stage of development... Olivia is taking the risk.... so Kudos to her.

As for the original Dr. Zamboni ..... No he is not trying to scam anybody.... He is driven by his observations, and strongly believes that this is a new way of looking into MS..... that might lead to a better treatment/ cure for MS!

Here is a link to the publications by Dr. Zamboni as listed in pubmed

As for ND.... I think it's both promotional and charity.... and I see it as a win win situation for both ND and Olivia..... it's for a good cause.. So Kudos to ND :)
 
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I did some reading about MS and CCSVI. It's unclear at this point if CCSVI is causally linked to MS...
Also, no 100% evidence that the proposed investigational procedure will be successful.

Here is the link to articles related to CCSVI in pubmed...... there are 48 in total

The key word here is "Investigational" it may or may not work..... but someone has to go through this stage of development... Olivia is taking the risk.... so Kudos to her.

As for the original Dr. Zamboni ..... No he is not trying to scam anybody.... He is driven by his observations, and strongly believes that this is a new way of looking into MS..... that might lead to a better treatment/ cure for MS!

Here is a link to the publications by Dr. Zamboni as listed in pubmed

As for ND.... I think it's both promotional and charity.... and I see it as a win win situation for both ND and Olivia..... it's for a good cause.. So Kudos to ND :)

*****************
Have you watched the episode of Canada's CTV's W5 that launched the news and excitement in Canada? You can view it here...
W5 : The Liberation Treatment : The Liberation Treatment, part one

His book was recently released... I'm dying to read it!
CCSVI as the Cause of Multiple Sclerosis: The Science Behind the Controversial Theory

http://www.amazon.com/CCSVI-Cause-M...WVU5XWC2&s=digital-text&qid=1305996200&sr=1-1
 
More info for those of you who are interested...

Dr. Hubbard's theory of MS


by CCSVI in Multiple Sclerosis on Friday, May 20, 2011 at 2:20pm

Dr. David Hubbard is a neurologist and founder of the Hubbard fMRI Institute and the Hubbard Foundation. He, and Dr. Jack Burks, were the only neurologists present at the recent CCSVI conference, although many neurologists were invited to attend. This was disappointing, to say the least. One would assume that neurologists would be interested in new research into the blood brain barrier and MS.

The following is a summary of Dr. Hubbard's presentation:

The first thing to note is that the current autoimmune theory of MS is still only a THEORY. There is absolutely no proof that rogue t-cells are what cause MS. This is an hypothesis.

Dr. Hubbard began by discussing the current autoimmune theory. MS drugs, based on EAE and this theory, have a 30% efficacy rate...about the same as placebo. The reason MS drug trials have to be so large and involve so many participants is that it takes that many people to make any statistical significance. The MS drugs are not a success story. They do NOT prove the autoimmune hypothesis.

Dr. Hubbard presented his very important insight into what he believes is causing the white matter lesions and destruction of myelin in the MS brain. It is very different than the current understanding that MS specialists propose with the EAE mouse model and the idea that myelin destruction is caused by an out of control immune system which is attacking itself.

Oligodendrocytes are a type of brain cell which form the covering of our axons. They make up the myelin sheath. Dr. Hubbard cites research of Prineas and Barnett, showing that the oligodendrocytes DIE FIRST in MS. They are not dying because of an immune attack of white cells....they die BEFORE the immune system is ever involved.

The ologodendrocyte shrinks and dies from the center of the cell. Only later do t-cells come in clean up. Macrophages also come in to clean up, this is a standard response of the body to tissue death.

"White cells just don't go chomping on the blood brain barrier...they are invited in."

So what is the "unknown factor" that is killing oligodendrocytes and inviting in white cells???

Dr. Hubbard proposes that this "unknown factor" is decreased perfusion, or slowed blood flow thru the brain. (Fans of the page will note that this has been the theory of Marie and myself, too, since the beginning of our journey.) Here's an earlier note on hypoperfusion and MS https://www.facebook.com/note.php?note_id=439394977210

The fMRI studies and Dr. Haacke's blood flow studies are confirming this theory. The thing about perfusion is that it affects both WHITE and GRAY matter. It is affects the ENTIRE BRAIN. MS is a disease of the entire brain....gray matter atrophy and white matter demylination. This theory is the first to address BOTH ASPECTS.

White cells are picked up by the edges of the endothelium, roll along and then are invited thru the tight junction to get into the brain's paranchyma.
MS is not a disease of an immune system gone awry. It is a disease where white blood cells are responding to injury, and are acting appropriately.

CCSVI creates a slowed perfusion, or slow flow of blood in the brain.
Decreased perfusion and reduced flow and stagnation in the vein causes a shunting of blood around the abnormal venule, the oligodendrocyte is not getting enough O2 and glucose. The oligodendorcyte dies.

Please watch all of Dr. Hubbard's research and listen closely. I believe that this is the answer, and connects all we KNOW and all we can SEE about MS brains.
http://www.youtube.com/user/HubbFound#p/u/39/Z1BP_xOQQlY

I believe this is MS....
- I thank Dr. David Hubbard for bringing the pieces together as a neurologist.
- I thank Marie Rhodes for bringing the pieces together as a medical writer.
www.ccsvibook.com
And I thank all the researchers who are ready to look at this new theory, take it further and begin the process of ENDING MS. For good.
Joan
247743_10150187683827298_110796282297_6729145_7199238_n.jpg
 
Wish you all the best with this Liv! :)
 
Sorry to hear about your condition.
Do you have any official donation Bank Account?
 
I am a multiple sclerosis sufferer, and a friend of Liv (Erica). My symptoms aren't as bad as hers, but due to the degenerative nature of MS they may someday be. As friends we share our stories and listen to each others problems. Thats what friends do. Liv has shared many links and articles with me, for which I'm grateful. My MS is a relatively recent thing and I will admit to still being in shock about it. To go from being physically fit and working, to severely disabled physically OVERNIGHT was a helluva shock. But I'm trying to work through it as best I can with the help of family and friends.

Until something of this magnitude forces its way into our lives, we simply can't comprehend what someone else is going through. MS is a mysterious disorder, and it's true there is no cure. Yet. But no one, in any of the articles I've read, has claimed this procedure to be a cure, miracle or otherwise. It is simply a way to relieve the symptoms of some people with MS. Afterwards, Liv will still have MS. And will have to face the fact that as of yet, nothing she can do will permanently solve her symptomology. But thats not really the point is it? The point is about trying to improve her quality of life. About actively trying to improve her situation. How many people actually try to improve their situation in life, instead of maintaining the status quo and constantly bitching about it? I'm sure we all know someone who fits that description.

I've read so many negative comments so far, they see the names and automatically jump to conclusions without trying to see what its all about first. Maybe I am taking this kinda personally, as it is hitting pretty close to home. But Liv has posted lots of info, and I for one intend to keep reading. After all, it affects me too. And yes, I will be donating to Erica's fund. I hope that someday, when my time comes, that I will be able as blessed with friends as she is.
 
I am a multiple sclerosis sufferer, and a friend of Liv (Erica). My symptoms aren't as bad as hers, but due to the degenerative nature of MS they may someday be. As friends we share our stories and listen to each others problems. Thats what friends do. Liv has shared many links and articles with me, for which I'm grateful. My MS is a relatively recent thing and I will admit to still being in shock about it. To go from being physically fit and working, to severely disabled physically OVERNIGHT was a helluva shock. But I'm trying to work through it as best I can with the help of family and friends.

Until something of this magnitude forces its way into our lives, we simply can't comprehend what someone else is going through. MS is a mysterious disorder, and it's true there is no cure. Yet. But no one, in any of the articles I've read, has claimed this procedure to be a cure, miracle or otherwise. It is simply a way to relieve the symptoms of some people with MS. Afterwards, Liv will still have MS. And will have to face the fact that as of yet, nothing she can do will permanently solve her symptomology. But thats not really the point is it? The point is about trying to improve her quality of life. About actively trying to improve her situation. How many people actually try to improve their situation in life, instead of maintaining the status quo and constantly bitching about it? I'm sure we all know someone who fits that description.

I've read so many negative comments so far, they see the names and automatically jump to conclusions without trying to see what its all about first. Maybe I am taking this kinda personally, as it is hitting pretty close to home. But Liv has posted lots of info, and I for one intend to keep reading. After all, it affects me too. And yes, I will be donating to Erica's fund. I hope that someday, when my time comes, that I will be able as blessed with friends as she is.


Thank you very much for this reply, Penny! You are always in my thoughts! :)
 
Got no problems at all with this whole idea and I hope it helps you Liv.

The problem I got with this is that Neverdie is the middle hand... I rather see 250 avatar meeting up and giving 50 peds each (thats not much :S) to you... I mean, 50 peds x250 is 12500 peds... It will take a miracle to reach that much taxes in hell from hunting I think... No idea how much people that hunt them

Anyway... Can't we all just make our own "event" to help Liv? :wtg:


LA event, 50 ped per ticket, hunt for 1 hour or 2 hours on a popular mob.. ticket profit goes straight to Liv's account where she can withdraw it to help her...

Anyone?....
 
Penny's reply was very touching, but I encourage my friend to not only keep reading, but to watch the many YouTube videos that have been posted by those who have had this treatment.
True, it is not an official curd, but it is the closest thing.
The fact that it has been shown to completely stop the progression is so incrediboy remarkable!
Zamboni's wife not only saw her current symptoms disapear, but she went for an MRI scan ever 6 months aftr.
The results clearly showed less and less plaques i8n her brain with each scan!
When a ,an with MS who had been in a wheel chair for 10 years, is now able to walk with a cane, and walk his dog every day - this is all the anecdotal proof I need.

I also have my own personal experience with this treatment, and so I know first hand that it works. I simply need stents to keep the veins open...
 
Got no problems at all with this whole idea and I hope it helps you Liv.

The problem I got with this is that Neverdie is the middle hand... I rather see 250 avatar meeting up and giving 50 peds each (thats not much :S) to you... I mean, 50 peds x250 is 12500 peds... It will take a miracle to reach that much taxes in hell from hunting I think... No idea how much people that hunt them

Anyway... Can't we all just make our own "event" to help Liv? :wtg:


LA event, 50 ped per ticket, hunt for 1 hour or 2 hours on a popular mob.. ticket profit goes straight to Liv's account where she can withdraw it to help her...



Anyone?....


For those of you who agree and wish to help, here is a link to my Liberation Fund Donate button on PayPal.

http://www.facebook.com/pages/Erica-Cowell-Liberationfund/184008458318779?sk=app_4949752878

No donation is too small.

In have not yet received many direct donations here yet... :(
 
More info - a Canadian's testimony

For any of you who have taken part in this thread, you may be interested in reading the following. It is the testimony of a Canadian who had the Liberation Treatment. His story is moving, and he now has his life back. He has also become an advocate to make this medical procedure available in our country.



A ‘New Hope’ for MS ---Tears filled the eyes of Tim Donovan

Tears filled the eyes of Tim Donovan, as he smiled and took a few people down the road of his hardship during the New Hope For Multiple Sclerosis 2011 Canada Tour stop in Gander, May 12.

“I almost lost my family.”
He sparkled when he revealed liberation therapy as a new hope, which can save lives. As a new man after receiving liberation therapy, he is on a rescue mission to ensure chronic cerebrospinal venous insufficiency treatment (CCSVI) takes its proper place in medical facilities across Canada.
“I’ve got my family back. So, do you think I’m excited? You can count on it. I want to share this with everybody across Canada,” said Mr. Donovan, founder of New Hope for Multiple Sclerosis.
The suicide rate for MS victims is seven times the national average. MS is a depressing and debilitating disease. Up until last August, Mr. Donovan was lying in bed for 20 hours a day. His life was passing him by. He felt helpless. So, when somebody came along and said there may be hope for people with MS, he listened. He was thrilled to discover it turned out to be accurate. There is new hope.
MS is caused by damage to the myelin sheath, the protective covering that surrounds nerve cells. When this nerve covering is damaged, nerve impulses are slowed down or stopped. The nerve damage is caused by inflammation, which occurs when the body's immune cells attack the nervous system. It has, in some cases, led to death.
“Canada loses 400 people every year. Somebody’s dying today to MS,” said Mr. Donovan, “and we’re allowing them to die because we’re not treating them. We now have something that may work.”

Liberation therapy, also referred to as CCSVI, was pioneered by Italian surgeon Paolo Zamboni. A balloon angioplasty is used to widen a vein in the neck, which is thought to relieve a build-up of iron in the brain. Many Canadians have been travelling abroad to have this treatment.
Mr. Donovan is appalled that CCSVI has not been offered in Canada, and is determined to bring it home. Through the generosity of people, he has been armed with an entourage, a vehicle and an RV to drive across the country to promote liberation therapy as a necessary alternative treatment in Canada.
“We’re still looking for fuel. It’s expensive. Every time we stop it’s $100, but this is all being sponsored by individuals and communities. People with MS don’t have money because they don’t work. I haven’t worked in 20 years. Joan and Pat Slaney took me into their home and they fed me steak last night. People like this make it all worthwhile,” Mr. Donovan said warmly.
He expressed gratitude to Mayor Claude Elliott to be one of the first municipalities, aside from his own in Fredericton, NB, to support his cause.
“MS is like cancer, in that many have been affected by it. It’s a good cause,” said Mayor Elliott, who presented a donation toward their cause last Friday at Gander town hall.
 
Nice bump....


and update on this story:

http://www.neverdie.com/rocktropia-...ivforever-aka-erica-cowell-finds-sponsor.html

NEVERDIE said:
For the past 6 months We have been building funds through our Hell to pay event for our Avatar friend Olivia livforever aka Erica Cowell. Funds were to be used to pay for an MS liberation treatment. The Event has been going Well and we had already started discussing the details. But thankfully Erica has found a Sponsor to organize her treatment immediately

We Wish her the Very Best With this Treatment.

With Erica’s Blessing, the Hell to Pay War chest accumulated so far will be Spread across future Hell to Pay events!

From the Entire ROCKtropia Community, we all Wish Erica the greatest Success with her procedure and a Speedy recovery
 
I have 2 accounts

After re-reading the article, I noticed that the fb account it's linking to is for Erica L Cowell not Olivia-LivForever. I guess they are one in the same, just two different fb accounts for the same person?
This is true, it links to my personal Facebook account. I do have an account for my avatar too though which is Olivia LivForever. My personal page has a few Entropian friends and TONS of MS friends I met around the globe whom I met on Facebook.Although a rich friend came through for me when I needed it most and NEVERDIE did not use the money originally raised for my Liberation fund, he was so concerned that it did not get me back on my feet again, that he bought and had shipped 2 expensive post-op leg braces to me! I could never have afforded them on my own, and will start wearing them in bed this week.Thanks again Jon for all you have done for me, and for continuing to give me hope every time I think there is none!And for all you who doubt his kind and generous nature, I have seen nothing posted about this on the Net. :ahh:
 
This is true, it links to my personal Facebook account. I do have an account for my avatar too though which is Olivia LivForever. My personal page has a few Entropian friends and TONS of MS friends I met around the globe whom I met on Facebook.Although a rich friend came through for me when I needed it most and NEVERDIE did not use the money originally raised for my Liberation fund, he was so concerned that it did not get me back on my feet again, that he bought and had shipped 2 expensive post-op leg braces to me! I could never have afforded them on my own, and will start wearing them in bed this week.Thanks again Jon for all you have done for me, and for continuing to give me hope every time I think there is none!And for all you who doubt his kind and generous nature, I have seen nothing posted about this on the Net. :ahh:

Thats fantasic news is great to hear from you on hear. Everytime i meet i meet up with you in game you all ways make me laugh.
 
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