PLEASE Help a very poorly little girl

Thanks Boro, Is it fantastic what these children did , or is it me ?
yes but children tend not to look too deep into things, they are not wanting to know where and what every penny of that 50 pence is going on and why they should be doing it for free without getting a cut

if only a few more people could give a couple of minutes of their time and publicise this we could all make an impact :rolleyes:
 
I cannot edit that video yet as I am at my moms in wales, when I get home I could add a title screen and an end screen detailing how horrible ataxia is, could this be used in the campaign, is this video good enough to go viral, I personally think so but as I said I am bias,I was there everybody was laughing all day long, they took the most money , yet there were face painting and balloon modeling.
 
totally right I see threads regular saying 10000 uvs a day how to monetise type thing
simple while you are working it out add this banner to your site and link to millies page or to ataxia for the non believers
also I am not into facebook or twitter obviously I should be (just getting started with facebook) and will but surely those with these accounts could tweet about this or post it to their friends it wont cost you a cent.
Come on you are all sitting at your keyboard
Do some good log in and send the message you will feel better for it

Thanks Boro, I love the banner, shame i am new had to delete link . I wish i understood seo, I would be there with you . I just wish other people could see the bigger picture as you do, the power of this forum is unbelievable, as you said give it to ataxia uk , friedreich ataxia research aliance babelFAmily org I do not mind which.
 
every country in the world has an ataxia charity , either promote or donate to those ataxia charity's in your country. I will repeat as lost in thread this is not about my daughter leaving behind a legacy , neither is it for my own notoriety. It is what it is. Exactly as on tin with NO hidden agendas. A cure for Ataxia
 
I wish the people with nothing nice to say would back the hell out this thread and keep there greedy little heartless opinions to themselves.

Nick it looks like it was a great day for Millie keep us posted on things.
 
asking for donations on this forum and expecting nice replies ... well, hardly is this going to happen.

You been a member for over 2 years....someone clearly helps you in what you need or you wouldnt keep using the forum, this forum is based on support, wether relating to IM or personal ....dont label or imply all of the BHW community have the mentality of the few who choose to make degrading, ill-informed comments...for the most part the majority of active members here are more than happy to help and support people in need .....
 
ill donate - i respect your attempt to help them, and if your a scammer i respect the audacity of your hustle. most of all, karma will work it's way to all of us, whether we are donors, scammers, or ones who suffer from illness. i prefer donor karma.
 
Dude, I don't know what kind of dontate button that is, but I pressed the paypal button and it requires me to fill in a bunch of passwords/names and personal information on your site as opposed to just going to paypal like any other transaction. In fact it is like creating and account, I will dontate if I can press a button and go to paypal and pay. There are 4 fucking tabs of data to input, even if you press the paypal button, you get re-directed to the page.
 
Dude, I don't know what kind of dontate button that is, but I pressed the paypal button and it requires me to fill in a bunch of passwords/names and personal information on your site as opposed to just going to paypal like any other transaction. In fact it is like creating and account, I will dontate if I can press a button and go to paypal and pay. There are 4 fucking tabs of data to input, even if you press the paypal button, you get re-directed to the page.
Hi , It is a 'just giving page', we use this in the UK because Ataxia UK can claim extra 28% Gift AID from tax payers on top of their donation. I would not accept any paypal payments. If you are having problems you can donate direct to Millie's Charity . Ataxia uk org donate . Thank you
 
Spreading the word to my 100k facebook friends/fans base.

Hope shes going to be well.
 
Hi,

Just sent some money (Ł50). I wish all the best for Nick, an thank you for hamd01 for opened this.
I'm living in middle east Europe, have 5 children and they are fine.

I think this is the worst thing on the earth if your child's health is not right.

FOR THOSE WHO WANT MAKE INVESTMENTS AND NOT DONATIONS:
I have some grayhat scripts and here is the deal;
There is script - a pingback server.
You can install it on your static site, just have to build some code into your html. (+ installl it)
The server will catch all the pingbacks. (I spent more than $200 on it)

It is good if you purchase service like: post link networks.
The blogs discover the target site (your) and pingback it if they find the autodiscovery code.
So you will know all the blogs where your links are and you can promote them.

I will send the script to a reputable member if he wants to test it (prefer a mod - Harro?) and if it good, I will send you it to Nick or hamd01.

They will send the script to the donators if they want. (I think who sent more than Ł20.)

Please pm if you would like it. (Nick, or hamd01, or mod)
 
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My take on things:

Whether people think this particular website is a scam or not, the case is on that real donation website meaning it is a real case...

If this guy really wants to help this girl he will have no problem with people donating through the official charity website. Or sending direct to.the family

Just a note which seems to be overlooked... Its very easy to find a real case including a childs last name and register a domain under a false name. That is why i personally would have no issue donating through the official charity site (which has been posted previously starts with an a) or to get in contact with the newspapers to find a mail address to post a cheque. Just a bit of common sense...

This might be a bit stupid but even if u think its a 50/50 chance of being a scam, at the end of the day we are taking that chance on a little girls life

All the best mate.
 
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Op...have you been a "philanthropist" in the past? Also asking the same questions to all those who positively think this is a legit thread.

Even if this is a legit situation, have you even ventured out of your European environment and ventured out to third world countries?

If you ever had, the same situation is 1000 times more radioactive in the "third world countries".

HMMM...
 
Op...have you been a "philanthropist" in the past? Also asking the same questions to all those who positively think this is a legit thread.

Even if this is a legit situation, have you even ventured out of your European environment and ventured out to third world countries?

If you ever had, the same situation is 1000 times more radioactive in the "third world countries".

HMMM...
While Millie may not be the poorest or the porliest child worlwide, and compared to some is very very lucky. The condition Ataxia which is what this thread is about is evil. Millie started above average , walking at 10 months , vocabulary of a 5 year old at 2, Millie was diagnosed last year and she is now on anti ageing tablets .It attacks every muscle and every nerve , very slowly, a slow death. I have to watch my daughter get worse month by month,year by year she is losing the use of her hands, next it wil be her legs the her speach then her life. There are also children going through exactly the same worldwide. If I lived in a third world country and my child had ataxia I would prey everyday that some rich guy(in their eyes) would do a website to bring attention to what is EVIL. I admit when a cure is found it will take a long time to reach third world countries, but it will get there. There are videos you can watch if you wish one is called
'stop the clock ataxia'
another
'friedreich ataxia corporation'
 
Hi all,
I have joined this forum for two reasons, one being that I build websites and think I am get some sue and help from here.
The other being that with regards to Millie, and her farther Nick, this is not a scam, and I can completely guarantee and prove that should I need to. I read about Milleis condition a few months back, and was completely saddened to hear about her story. I also thought that a young girl fighting this condition, and yet still wanting to raise awareness, funds, and encourage other with the condition, and young children, that you can still live your life, is amazing. I have two small children and could not imagine what it would be like for them to to be ill like this, or how hard for us it would be.
Anyway after reading about Millie, I wanted to help, but not having much money, I thought I would put my skills to use, and offered to build a word press site, with the theme of exactly how Millie wanted it. This meant that they could quite easily keep the site updated. I didn?t want any money or named as the site builder, no advertising for myself etc, just trying to give something back and help out.
I also arranged for mille to have a professional photo shoot, as every girl loves to feel special, and I am happy to help out in anyway I can.
I can understand that some may have thought the post was a scam, we all see it all the time,. But in this case it was not a scam, and if some of the negative people had taken a few mins to use google, or even look at the site, it would have saved a lot of unpleasantness for all. Surley the time spent on this single post could have been put to more better productive use.
I just hope that people will learn, that you should never judge, you should never assume, and also to the Nick and mille that are people who are happy to help and were not all that bad.
If you want to verify that I am real, not a member of the family or anything, just a young lad helping out then, please feel free to send me a pm.
I have been reading around the forum, and its seems a useful and helpful place (most of the time)
X x
 
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