How Second Life Makes Life Better For A Disabled Person

By Deaflegacy

Hello, everyone!  My name is DeafLegacy.  As per my name, I am deaf.  I have been deaf since birth.  I have managed to do just fine when my Mom learned sign language.  I was a lucky woman to have my Mom, who knew sign language.  Unfortunately, I lost her in 2013.  I miss her very much.

I came to Second Life three years and five months ago.  Someone mentioned Second Life, and that caught my attention.  At first, I was a shy person, using a female human avatar.  I wasn't sure how to get more Lindens.  As days went by, I started to know more about this virtual world.  For one, I know now how to get more Linden dollars, from winning contests, to Second Life jobs, or buying them with real money.  I do that once a month to make sure that my lots are paid for.

I find this amazing that when I first started using Second Life, I moved into an apartment on Cape Heron.  I have had two apartments but not at the same time.  I would remember my old living spaces with fondness.  When I was living in an apartment, I would be looking at houses on the parcels, and wanted to live on a parcel.  One day, I got parcels.  I can't say how many parcels I got because for some reasons, it's not right.  So I would just say that one day, I got some parcels, and ever since then, I have been making sure that I pay the rent.

Why am I telling you this?  Well, I can give you a few reasons.  I can tell you that I was lucky in finding Virtual Ability, which is a group for people with disabilities.  They have been there for me ever since I have been a member.  I can also tell you about writing for the SL Newser.  I was so happy when Bixyl Shuftan hired me.  I can definitely tell you that my desire to write never stops growing, even though I have a disability. I mean, when it comes to writing, who cares about the writer's disabilities?  We care about what the writer is writing about.

Second Life had helped me out a great deal since the day I signed up.  I have no regret in joining Second Life, and I hope to continue on as a member of Second Life.  In a way, thanks to Second Life, I'm now a writer, and I got lucky to have a partner, Six String (roleplayismylife).  I love Six String very much.

Thank you, Second Life, in giving me many chances.  I will never forget that.

Deaflegacy

Fran Seranade of Creations for Parkinsons

By Deaflegacy

"Parkinson's is a progressive neurological disease." said Barbie Alchemi. "My Father died with it and my Mother has it now. But I have learned that although my Mom has  Parkinson's, it does not have her!"  Her mom would be Fran Seranade.  They have a Second Life Parkinson's Support Group that has been meeting for six years.  The members have all learned that they are still themselves, their own personalities, and can express their creativity and emotions the same as always.

"Yes my Mom just turned 90 'Years Young' as she likes to say (laughter)," spoke Barbie when she was asked about Fran's recent birthday party.  "She thinks of Second Life as the 'Fountain of Youth'.  Inside she feels very young, yet her physical body is getting old.  The wonderful thing about Second Life is that here she can feel and experience life as young as she looks."

Barbie went on to say that Fran had two birthday parties.  The first party was seven hours of live music at their CP Swing 40's Era Dance Ballroom.  Over 200 people dropped by to share their love with Fran. They have raised 180,000 Lindens for the Michael J. Fox Foundation for Parkinson's Research that day.  "That is $700 US Dollars!" said Barbie.  Barbie also added that Fran loves to dance at their new CP Swing Ballroom because they play the music of her teen years, which brings back fond memories for her.

"She was quite the dancer in her day. She and her partner could clear the floor." said Barbie.  "The second Birthday Party was even more amazing in some ways."

Barbie explained that six core members of their SL Parkinson's Support Group have become so close after meeting together every week for six years that they all decided to fly from all over the country to be together with Fran on her real-life birthday.

"It was the most wonderful experience," said Barbie, "We have all grown to love each other so dearly, and when we all met in person, it was as if we had known each other forever.  Second Life has brought a depth and meaning to our lives that we all treasure."

They have 30 members in the Parkinson's Support Group, but not everyone comes all the time.  They usually have around eight members who are there every single week, unless something in real-life prevents them from coming. It is at a perfect size so everyone gets a chance to share as well.

"Mom started the support group in Second Life, and asked Tredi (Dr Donna Davis) to facilitate each week. She presents a meaningful topic that we discuss." said Barbie.

According to Barbie, they have raised almost $10 million Lindens since they started, and that is $40,0000 US Dollars for Parkinson's Research. She also shared some information about the Parkinson's Support Group.

The information is below:

THE STORY OF CREATIONS PARK ~ Grown with Love
Our RL Dad died with Parkinson's and our mother, Fran Seranade, has it now. To quote her "I may have Parkinson's, but it does not have me." At 90 "years young", she is active in Second Life and is thrilled to see herself running and dancing again. We have built everything on Creations Park with LOVE. We hope you can feel that love while you are enjoying yourself here.

OUR MISSION
It is our Creations Team Mission to use our love and talents to make a difference in both the RL and SL worlds. We create experiences to stimulate Hearts, Minds, Bodies and Souls. It is our goal to help find a cure for Parkinson's which will then lead to a cure for all neurological diseases. Come share your love with us and help us find the cure!

***VIDEO***
PLEASE be sure to watch our award winning video about the benefits of SL for our RL Mom who is 90 "years young" and has Parkinson's. Ebbe Linden (CEO of Linden Labs) has called this one of the most important video ever made
[13:41] Barbie Alchemi:  about Second Life! This will inspire and touch your heart!
The Drax File: World Makers- Episode 13
 http://www.youtube.com/watch?v=nyiiWxNguGo&feature=youtu.be

DONATIONS
100% of all donations go to Team Fox for The Michael J Fox Foundation for Parkinson's Research. We believe it is important for you to know how your donations are being spent. Our family covers all tier and expenses. All Donations are directly wired from Linden Labs to the Foundation. The MJFF has the top rating from Charity Navagators and has the lowest overhead of any major charity, giving 89% directly to the most promising research!

"It is not our challenges that define us, our actions do." - Michael J Fox

"If someone would like to join our Parkinson's Support Group, then need to contact me for an invitation to the group," Barbie told me.

Barbie was invited to NYC to meet Michael J. Fox in person as a result of the important work they do on Second Life to help find a cure for Parkinson's.

The SLurl for the main landing spot is: Creations Park (90,164,36)

Deaflegacy

Interview With Jadyn Firehawk of "Pixel to Pixel"

By Deaflegacy

Jadyn Firehawk discovered Second Life in 2009. She found it because she had a Flickr site for her real-life photography.  Noticing quite a few groups there that had names with Second Life in the name, it made her curious. Jadyn googled about Second Life, and that's how she found it.

Jadyn created an account, and at that time there were "community gateways" for entering Second Life from the main website. She saw Virtual Ability as one of the gateways. At the time, she had been very active in a bipolar disorder support group chatroom online. It interested her that there was a disabilities support group on Second Life.  She Joined the Virtual Ability group, and began exploring Second Life from there.

Jadyn has bipolar disorder and post-traumatic stress disorder (PTSD).  She has chosen to be open with people about that as a part of her personal activism for mental illness, hoping that it will help it become less stigmatized by society. When asked about some of her accomplishments in Second Life, Jadyn spoke of her background. Jadyn is a former university professor, but had to go on disability due to the bipolar disorder and PTSD beginning in 2001.  It improved a little in 2005 and she was able to go back to work part time.  When Jadyn came into Second Life in 2009, she was still working part time.

 Jadyn had a friend from the bipolar disorder chatroom, who decided to try out Second Life, too. He was young, in his early 20s.  He was in school and on disability, and had very low income as a result.  Her friend didn't have a single dime to spare to spend in Second Life and Jadyn understood exactly what that was like from her own experience having been on disability, so she gave him some Lindens every week so he could have a bit of fun. She enjoyed helping him and it gave Jadyn the idea of starting something up in Second Life where others could maybe do it too.  That's when Jadyn created the Pixel To Pixel Foundation and it's been going in Second Life ever since. 

The P2P Foundation receives donations from very kind and generous people throughout Second Life.  Then it turns around and distributes weekly stipends to people who are on disability so that they can do such things like rent a home, buy some clothes or furniture, upload textures, or get some building supplies.

The P2P Foundation has just celebrated its 7th Year Anniversary in the Summer of 2016. Jadyn said, "The P2P Foundation's Director avatar account, named Pixel Falconer, has a rez date of June 29, 2009. That's what we consider to be the founding date. That avatar is the one that receives the donations, holds the funds, and disburses the stipends."

The P2P Foundation currently supports 22 people who are on disability with weekly stipends of L$500, so the total amount that it fundraises and disburses is L$11,000 a week. "It's a challenge for a small organization to keep up that kind of fundraising!" said Jadyn. "We'd like to help a lot more people, so we're always looking for new donors. There are over 20 people currently on the waiting list."

In order to sign up for P2P Foundation, there are two things - recipients must be "on" disability, and not just "have" a disability and they must be willing to provide a copy a document showing that is the case. "With health-privacy information protected, of course," she added, "This is so that they have been pre-screened already by an agency for having medical proof of disability." said Jadyn.  She went on to explain that some donors express concern about possible abuses of our system.

Jadyn added that although she had to disability-retire from her career in 2010, she has been able to make an income in Second Life from teaching tips at Builders Brewery and from her shop, Maganda Arts, and draws no funds from the foundation. The Building Tricks series that she teaches at Builders Brewery now includes 15 different classes. At Maganda Arts, she sells a wide range of things including historical homes, furniture, kinetic sculpture, and real-life photography.

When asked about other accomplishments besides the P2P Foundation, Jadyn spoke about the Yosemite sim. She explained that the other reason she wanted to tell me about her former career as a university professor is, when she became disabled in 2001, she had been working on a book about Yosemite National Park.  Jadyn's research specialty was national parks and protected areas. When she was unable to work, in a sense, she also "lost Yosemite". "And it was a great loss to me. Yosemite is my favorite place in the whole wide world. I've been there so many times, I've lost count."

She has just recently created a virtual Yosemite National Park in Second Life, and it opened in July 2016.  According to Jadyn, its peak visitation so far, according to Linden Lab's traffic measurements, has been 8434. ("Traffic" is defined by LL as "the cumulative minutes spent on the parcel by all visitors to the parcel within the previous day") For a few weeks, the main park, Yosemite Valley (Forever Wild) was in the Editor's Picks in the Second Life website's Destination Guide. It is now in the Nature & Parks section, along with her Shinzen Japanese Garden, also located at the Yosemite sim.

"I see it as, I lost Yosemite in 2001 when when I became disabled.  But now, 15 years later, I have it back again!" said Jadyn.

Jadyn also mentioned the Ethnographia Project, which expresses her story of experience with disability and Second Life. "It's not quite complete yet though, a work in progress," said Jadyn.  She added that it is open to the public. However, to the writing part, Jadyn is still working on it. 

Jadyn went on to describe Yosemite Valley (Forever Wild). "Yosemite Valley (Forever Wild) is one full sim in size and there's horseback riding available here for free." said Jadyn.  "And it's a nice place to relax and enjoy the scenery, and meditate or visit with friend."

The landmarks are:

For the Ethnographia Project: http://maps.secondlife.com/secondlife/Ethnographia/175/78/32

For the P2P Foundation Office: http://maps.secondlife.com/secondlife/Clairehaven/130/136/24

For the Yosemite Valley (Forever Wild) : http://maps.secondlife.com/secondlife/Yosemite/192/64/2652

For Maganda Arts: http://maps.secondlife.com/secondlife/Yosemite/148/196/1253

For Shinzen Japanese Garden: http://maps.secondlife.com/secondlife/Yosemite/77/215/21

Jadyn also mentioned the Building Tricks class series at Builders Brewery.  I have been to some of these classes and they were fantastic.

The class tutorials landmark is: http://maps.secondlife.com/secondlife/Yosemite/168/220/1261

The Builders Brewery is: http://maps.secondlife.com/secondlife/Builders%20Brewery/128/193/23

Deaflegacy 

Gemma Cleansalte wrote on Virtual Yosemite in July 2016.

What Second Life Means From A Disabled Person's Point of View

By DeafLegacy

I remember the first time I've heard about Second Life. Someone was talking about it and I asked him what it was. He told me that it was a virtual world. I said that I'd like to give that a try.

That was about a year ago. I have not had a regret when it comes to signing up for Second Life.

My name is DeafLegacy and I am deaf in real life. In a way, Second Life is a blessing because on it, I do not have to worry about talking. I have a speech disorder in association with my deafness. On Second Life, I am able to join some groups like Virtual Ability. I even signed up to write for the SL Newser. I'm not just a reporter. I'm a photographer as well.

To summarize it up, I'm a writer no longer trapped in her own world. Second Life had provided me with many different worlds where my deafness is not as important as it is in real life. Why did I say that?

Well, in real life, if I want to have a conversation with a hearing person, I'd need to be really good at reading lips as well as having some paper and pen. There's interpreters as well for medical appointments. It's not as easy as one might put it.

But on Second Life, I can have a conversation with anyone via the text mode without worrying about any misunderstanding that would rise from real-life conversation.

At least, whenever I go on Second Life, I almost always go to my apartment on Cape Heron. It's a beautiful apartment. In real life, I don't have an apartment. I live in a house with five other people. To put it this way, I'm the only deaf person in the house. Being deaf does not make it any easy. It tends to make it complicated. But on Second Life, I don't have to worry about that. The only thing I have to do is just be myself. Second Life had given me that chance and for that, I'm very happy.

I hope to continue using Second Life, even if it grows into something else. They are talking about it. I look forward to the day that happens. Until then, I'll keep on using Second Life. I can't say the same about the other people with disabilities, but Second Life is the best thing that happened to me.

Why? It's simple. Writing was my lifetime goal. Second Life just happened to make it come true. Now, I'm a writer both on Second Life and in real life. I'd say that's a chance I have to take and I did take it.

That's the best thing I ever did in my life. 

Deaflegacy

Reader Submitted: Thank You Virtual Ability

From Alysabelle Resident

When I first entered Second life, I knew nothing about it. I had a friend who wanted me to join for about two yearsm but my life was busy as most people are and too busy for a place called Second Life. But then one day I wasn't as busy as I used to be, and with continuing asking by my friend to join. I did.

Well here I was. I called it "Never land." I didn't understand the concept, my friend ended up going through PTSD in real life so he was barely around. I was confused in Never land. There were a few people that helped out over time, and then one day I was looking for a place to live. I lived on a platform where actually the owner of the sim was making passes at me. It was disturbing to say the least. I know this can happen to anyone and it happened to me.

With the help of a friend in Second Life, I came upon a place called Cape Serenity. As I teleported to the place, I was amazed by the community feel even though no one was around at that very early morning. I was enchanted. I had never seen a place like this before. I really felt this 'home' feeling. Then I contacted Ladyslipper Constantine, who is actually the caretaker of the sim. I wanted to know how much the rent was. After a few hours, I got an IM back from her and that very day. I rented a piece of land. I was so excited, I felt. I stood there for several hours just staring at the entire sim. Smiles. She was extremely welcoming and gentle and kind.

 I believe the following day Ladyslipper Constantine she shared with me her hearing problem and at that point I had not shared my hearing problem with anyone.  I wanted to be treated just like anyone else who didn't have a disability and I figured Second Life would provide this for me. But it was getting difficult to mask my hearing problem. I felt it was weighing me down in some respects. I couldn't hear everything and I couldn't hear everyone. But what I didn't know, after I decided to open up about C.A.P.D. (Central Auditory Processing Disorder), was that my friends that I had made knew something was different about me but they just couldn't put their finger on what it was.  As Ladyslipper shared about her hearing problem, I found myself sharing this information with her about my physical hearing problem even though we both didn't have the same hearing issue.

That was the start of my own journey in sharing with others about Central Auditory Processing Disorder. I knew if I opened up, it would be a challenge. After all its not every day you hear about this particular disorder. What I didn't know that Cape Serenity was part of Virtual Ability. Well I didn't even know what Virtual Ability what it stood for. I eventually was told, so imagine here I was landed on a sim called Cape Serenity part of Virtual Ability and here I was with a physical hearing problem.

The  mentors at Virtual Ability through time helped me with not just opening up about my physical hearing problem, but how to cope with it, how to deal with people who have such disbelief, which by the way I really understood them more than they realized only for the fact that after all its not that well known. C.A.P.D not as well known as other disabilities, but to be honest there were moments I wish I didn't say anything about C.A.P.D.

I learned that even though people have disabilities they have other gifts they are able to share, that there is a purpose a meaning behind everyone, no matter what disabilities you have. Most importantly for me is I met these wonderful women who have different hearing issues, and I found out even though we don't have the same ones we all have certain things in common none of the less. Listening to their stories of how they have been affected in real life or Second Life with a hearing disability, they gave me a gift, the gift of  strength that under any circumstances that you forge on and believe in yourself. And it really doesn't matter what anyone thinks or feels, that you are important in this world and no matter what you have to deal with you are still important. They are strong, those women whom I met in Virtual Ability. They say strength comes from wisdom and they are very wise from Gentle Heron, Ladyslipper Constantine, iSkye Silverwebm Treasure Ballinger, Treacle Darlandes, and Winter Wardhanid and countless others.

I'm so grateful they share with people like me who have a disability and those who have other disabilities. I"m so grateful and continue to be how much they have helped not just in Second Life but in real life. How they give their time to mentor those like me they really care and they don't do it for any other reason then a need to help people. They are selfless they mentor from the heart. They embrace you when you are down they give you hope, encouragement and belief in one self. They give you courage to rise above, they help those who need help and help them to become an even better person then you are, what is the expression that comes to mine I have heard before, they give you wings to fly... I will always be profoundly grateful for those who are part of Virtual Ability, that no matter where I go where I am they are always in my heart, Thank you.

Alysabelle

Interview with DJ Keao, Creations Park's "Blind DJ"

By Bixyl Shuftan

Recently at Creations Park, a Keao Resident began DJing for events. This might not seem to be unusual, except for one thing. keao was announced by Creations as a "Blind DJ."  Second Life Newser recently had a chance to interview her.

Bixyl Shuftan: "First of all congratulations on your DJing debut."

Keao: "Thank you!"

Bixyl Shuftan: "To begin with, well, blindness sounds like a pretty hard obstacle to overcome. How were you able to perform?"

Keao: "Well, most people have a lot of stereo types about us, saying that we can't do anything at all. We can, with a lot of confidence, the willing to do something to prove them wrong, and the technical know-how. It takes guts and the skill to learn, and mostly on my part determination, and others as well."

Bixyl Shuftan: "How did you first hear about Second Life?"

Keao: I heard about it through one of my other friends who is totally blind, sadly, he doesn't come on, because he wants Second Life to be more operating system spread out. He wants things to work with google, plus windows, but he wants a client that is blindness accessible. I've been here for 4 months, and the possibilitys are endless."

Bixyl Shuftan: "What kind of client have you been using to get on?"

Keao: "I'm using a client called Radegast, we need more developers for it for sure, it's a text based client. It's lightweight. Do you know Celene Highwater? She is a Radegast mentor. I amaze her every time when I find cool places. She saw that I was determined to learn how to use Radegast, and how Second Life works. She always saw a lot of people who are gammers.
Not much of the blindness comunity knows about SL."

"This is my place, by the way, that Barbie created for me to have a home in Creations."

Bixyl Shuftan: "Looks nice. (smile)"

Keao: "You bet, and if you need pictures, we can go up to the dance club."

Bixyl Shuftan: "If you like."

Keao: "Ok, I'll teleport you."

We then headed to the dance area in question, at (120/138/4056). There happened to be two couples there, dancing to the music stream. Keao headed to the DJ booth.

Keao: "I've been doing live broadcasting on internet radio for almost five years now on different stations in real life."

Bixyl Shuftan: "That's interesting. How did you get your start there?"

Keao: "It started in 2004, when I heard one of my good friends who has his own production company broadcast a show called northern lights, I couldn't believe that other djs who are blind got the technology to do it from there own homes. At the time I was about 14, and in high school, my dream was that I wanted to be on radio somehow. Here in Hawaii, you can't do it in a studio nowadays without going to a school. What I did was I tuned in to an internet station called ACB Radio Interactive, and instantly I was amazed, a lot of these djs are vollenteered to do it for free. It opened a lot of doors for me. My fiancee in real life is a ham radio operator, I know a lot of blind friends who do ham radio work who are blind and visually impaired."

Bixyl Shuftan: "What are some of the stations you've performed on?"

Keao: "Some of them are mostly ran by blind people, some of them are Team FM from the UK, Top Tunes FM which is from the same state, Mint FM for a while, Mojo Radio which was my first station, Radio Free Dishnuts, The Global Voice, Radio For All, and Tree House Radio, ruted in great music. The ones that are no more are Top Tunes FM and Team FM. The one that are still going is the Global Voice You can check out our site at www.theglobalvoice.info and treehouse radio, it's www.treehouseradio.com . The Global Voice is run by a lot of blind people, and we have some sighted people. Not a big number, but what they do is they help us on either youtube or facebook or twitter stuff."

Bixyl Shuftan: "Did it take long to find a place in Second Life to DJ?"

Keao: "I had a few in mind, most people wanted me to get familiar with it, I would say not too long, I was talking to Barbie (Alchemi) and she had an idea that I could DJ. She didn't know at first until I mentioned it

Bixyl Shuftan: "Where did you find out about Barbie and Creations Park?"

Keao: "I found about about her and Creations Park one day by attending a poem reading event that they have weekly here up in the tree house. We started talking about her mom, she was blind when she was a little younger. Creations Park has given me the opportunity to be creative and to be free, I am somewhat of a shy person. This place changed my life in a lot of ways."

Bixyl Shuftan: "Nice, in what ways may I ask?"

Keao: "Let's see. ... It has made me a much observant person, I can sense people by the way that they act, and how they are around each other in real life, even by their personalities. I can tell that a lot of people who I know in real life I don't want to get along with at all or who are trust worthy."

"My goal in real life is to become a massage therapist. The hard part is finding the right school, and to always do a great interview."

Bixyl Shuftan: "A massage therapist? What inspired this goal?"

Keao: "I can see peoples hearts."

Bixyl Shuftan: "Besides Creations, do you DJ anywhere else?"

Keao: "Nope, only here. I see Parkinsons as a disibility in a way, when Fran moves around as her avatar, she knows that she can do things. I can see myself in the same way."

Bixyl Shuftan: "Besides DJing, what else do you do in Second Life right now? I think you mentioned going to places."

Keao: "I am also the music manager here for Creations.  I help find good singers and performers. I have a few in mind who are big names up in Second Life."

Bixyl Shuftan: "Oh? Whom may I ask?"

Keao: "Voodoo Shilton, Stephanniyah Sinatra, Liz Aday, Parker Static, Long Paush, The Balladeer, and Savannah Coronet. And also Caasi Answer. Oh, and one more, Sara Marie."

Bixyl Shuftan: "Besides this, did you have any future plans in Second Life?"

Keao: "Through voodoo's group, I've met a lot of great people who accept my disability. I've met a lot of friendly people who are willing to help me out."

Bixyl Shuftan: "Was there anything else that you wanted to mention?"

Keao: "Oh, I forgot to tell you that when I got started in Second Life, I started out in a place called Virtual Ability Island. They have a lot of people with different disabilities."

Bixyl Shuftan: "How did that go?"

Keao: "It went really well. Most of them helped me out with a lot of the clothing and outfits, and the visual stuff (laughter). And wardrobe malfunctions. So Barbie helped me link outfits together, so it will be easier visually, and I know what I'm wearing (laughter)."

Bixyl Shuftan: " 'Wardrobe malfunctions?' Heh, have those been a problem?"

Keao: "Oh yes! You should have seen me when I was at the Oceana ballroom when I first started out. I had no idea I was naked! (laughter) Until someone helped me get a gown."

Bixyl Shuftan chuckles, "Have you tried other types of avatars, such as furry or dragon?"

Keao: "For the longest time I was at the Ballroom, (I) didn't know what other sims were out there until I found Creations Park, and also a popular club I go to at nights called Rise after Dark."

"I have a tiny avatar that is a dog. I would love to get a dragon one of a fairy."

Bixyl Shuftan: "I guess that's about everything. Thank you for your time, and good luck (smile)."

Keao: "Thank you!"

You can catch Keao perform at Creations Park. Drop by to get a schedule of her performances.

Bixyl Shuftan

Addition: Keao contacted me after the interview.  She told me she wasn't just legally blind as I first assumed, but, "I am totally blind, I forgot to tell you. I can't see anything at all." To get about Second Life, she uses, "an open source screen reader called nvda. It's non visual access desktop. It reads in speech, and converts everything in to text." When asked if typos are a big problem for it, she told me it's not, "it doesn't care if you use wrong spelling."

She went on more about her real-life plans, "I wanted to become a massage therapist because I've been using esental oils, and I would love to learn more of the techniques. Also, the practice is good in Hawaii, a lot or some blind people want to do that hobby. It's the number one career because it deals with hands and I would love to learn more of the techniques."

The "Buddy Walk" Downs Syndrome Bennefit

On March 21st at the Palladium and Platinum sims, a fundraiser was held to raise donations for Downs Syndrome research: the 4rth Annual SL Buddy Walk. Throughout the period, nine musicians performed at the stage at Platinum, beginning with Mankind Tracer at 2 Pm SL time:


Mankind will be performing live today at "Buddy Walk" to benefit Down Syndrome! All live! All Acoustic! All ROCK! Bring out your friends and let's help raise some awareness and maybe some money!



Showing up at the landmark just after 5PM, I saw that the dance floor went across two sims, one third of it and the stage over the sim crossing from the other two thirds. Maximillion Kleene was performing at the time to an enthusiastic audience, and just after 5:30PM the total raised hit 50,000 Lindens.

People could donate to various kiosks set up around the place, "Donations collected from this event are given to NDSS! you can find the kiosks at the landing point, both sides of the venue entrance and both sides of the stage." Most Lindens donated went to the unit next to the stage which also gave the total amount.

Both the volunteers and the dancers cheered each other on as the total went up, "We are so happy to see everyone today at the 4th Annual SL Buddy Walk," with occasional announcements going up.


SL Buddy Walk Announcement shouts: ++++++++ March 21, 2012 marks the 7th anniversary of World Down Syndrome Day and for the first time in 2012 this day will be officially observed by the United Nations. Each year the voice of people with Down syndrome, and those who live and work with them, grows l

SL Buddy Walk Announcement shouts: ++++++++ There are more than 400,000 people living with Down syndrome in the United States.

SL Buddy Walk Announcement shouts: ++++++++ Down syndrome occurs when an individual has three, rather than two, copies of the 21st chromosome. This additional genetic material alters the course of development an …


Checking in again just after 10 PM SL time, Edward Kyomoon was performing for the final hour. Volunteer JL Zinner shouted "We are at $136,673 raised..... our goal is to beat last year which was $156,000L. Just an hour left to do that!!" Taking a look at the main kiosk, the total was actually 139,674 Lindens. The final total, listed in the event's blog, was 143,283 Lindens, with 506 residents visiting that day. The stage was not a permanent set, and was gone the next day.

The volunteers suggested three links on the Internet for people to check out, www.ndss.org , www.buddywalk.org , and www.worlddownsyndromeday.org .

For pictures of the 2011 event, check the Flickr.

Bixyl Shuftan