Thanks and more thanks

Have you read the Thanks page lately? As always there’s many people to thank for supporting me in my efforts to put MG on the map.

Like the producers of our T shirt, who are mentioned in the Sponsors section under Business Contributors …

and then there are people I have only met online and some I met face to face on the trip, too, who are mentioned in the Individual Contributors section.

…… and then there are others who have supported the MG Awareness campaign by providing their services at cost or less than cost …. like mechanics and VW clubs mentioned on the Thanks page, and individuals who have made items to hand out or to sell for our petrol fund, like Kerri of Kerri’s Kreations, who has MG …. or Lauri Perry.

………… and then, most importantly, there are the people who send me messages and thanks on email or Facebook or here in the comments/reply section (at the bottom of pages like this), who keep up my spirits and made me realize that I am doing something to make a difference, however small it may be.

…………… and most of all, there are those with MG, who humble me when I think of them and make me realize that my ills are small in comparison. They are my inspiration and raise me up when I lack energy. 

Amy, one of our supporters who has MG, wearing a VW4CAUSES T shirt

The point is everyone and every contribution is as important as everything else and the internet is enabling us all to come together to make my campaign for MG Awareness possible. Every link in the chain is as vital as every other link, i.e. each one of us is as vital as another, and I am praying that our connections with each other continue and that finally we will connect with those who can shout loud enough to put MG firmly on the map and on the right road to finding a cure.

THANK YOU so very much.

 

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Isle of Dogs Photo Shoot for MG Campaign

Photos of our VW4Causes photoshoot for MG Awareness have been posted at http://www.facebook.com/media/set/?set=a.10151203623417445.478969.203679777444

I’ll add them here soon so you can see them if you are not a facebook user, but still have many pics to edit first.

See you later ………

HERE ARE A SELECTION OF PHOTOGRAPHS ….

VW lineup on the Isle of Dogs by Anton Gervase Murrells

 

One of the VW Club guys modelling the MG vest. Hopefully by now all of our readers realize that MG is not the classic sports car, but the auto-immune disease. Copyright by Carole Brown 2012.

Two budding MG enthusiasts!!! They're already members of the Paintscrapers VW club. Wonder if they'll drive for VW4CAUSES one day? Copyright by Carole Brown 2012.



Our VW line up. Copyright Roo 92 Photography.

VWs in the park, photographed by Sharon Read, edited by Carole Brown.

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Isle of Dogs Event – 20th Oct 2012

Be the first to spot our Green Split Window bus  (ABW xxxL) around Canary Wharf AND Island Gardens, London E14 midday-ish today (Saturday 20 October 2012) and then tweet our full number plate with location and/or post a photo on our Facebook page to win a car sticker of ‘The YesWeCan CamperVan no.1

Bumper sticker

 

If you tell us what MG stands for, we’ll enter you for a bumper prize !!! :)

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WHAT and WHY

There’s a lot of information on this website, so if anyone asks you WHAT I am driving for and WHY, then please refer them to this page or send them this link … http://vw4causes.org/mg-awareness/

 

 

You’ll be doing us a great favour. THANK YOU VERY MUCH :)

 

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Reader Comments !!!

There are some amazing reader comments coming in this week .. you have got to read them … look to the right hand column and scroll down …. underneath the videos, you’ll find ‘Reader Comments‘.
If you then click on the name of the comment, you’ll be able to read it and any other’s sent in for that same blog post.

This reminds me to say there’s a lot of information on this website – take a look around and you might be surprised :)

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Tribute to an MG Warrior

Hello Mum, I wish you were here today, 11 October 2012, to celebrate your 88th birthday.

I’m going to sit in the garden at number 13 – your home when you were diagnosed with MG and now my home (whoever would have thought that!)

and raise a glass to you … and ….

 

…. do something silly, also, to pay tribute to your sense of fun!

 
 
 

Perhaps you can whisper in my ear what you’d like that to be :)

 

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Uplifted but then ….

I just re-read the blog post I wrote almost a year ago, entitled “An amazing 48 hours“. And then I added a comment of my own to those of others ….

It’s 10th October 2011 and I am in my hometown of London. I just referred to this blog post in a reply to a new member of my VW4Causes facebook group who’d asked for some information about my reasons for doing this work and driving across the USA.
It’s actually very heartwarming for me to read what I wrote almost a year ago and to recount how I felt then. I didn’t know what lay head. And neither did I know that rather than 5500 miles and 5 months, I’d drive 7853 miles over 7 months!!!
Now I can’t believe that I’m contemplating doing more driving for MG awareness. Maybe I’ll stay a little while longer here in Great Britain to reflect on the most productive parts of the trip and see if this time I can get some corporate sponsors to partner with vw4causes and engage the media more so that our message can be spread even further afield.

At the same time I am also mindful of how a few days ago I felt very sad to read a post from a lady with MG (and three other auto-immune diseases) with whom I had been attempting to plan an MG Awareness event in Georgia, USA. Debbie, whom I met last December and is one of the most courageous, determined people I know, wrote how awful she felt when she was met by a lack of enthusiasm from others. She has had to shelve the event to next year and in the meantime her health has suffered a set back. She told me “If I had cancer instead of MG, it would be a whole other story”.
I know exactly what she meant. By now I’d be planning how to get my VW bus to Georgia to support Debbie in her efforts. Instead we are wondering what we can do to make a Spring event a success.

October in the USA is Breast Cancer month, and now I am here in London, I can tell you it is the same here, too; at least my local Wal-Mart owned Asda store is filled with pink ribbons. How I would love autoimmune diseases to have that kind of support. I keep imagining that one day the Susan G. Komen Foundation or another cancer charity will give some of their money to charities that support women with illnesses that are autoimmune in nature (75% of all cases occur in women – source AARDA).

Please do not take my comparison with cancer as me saying I do not feel compassion for those with cancer; I do care very much. Yet as an ex Pharmaceutical executive and biologist, I know that the research efforts for a cure for breast cancer (and most other cancers) will carry on regardless of whether anyone raises another penny or not. What concerns me more is that autoimmune diseases are a whole other picture.

Why is it, when we know that more people now have autoimmune diseases than all the cancers, that these diseases are still largely ignored and when it comes to funding for research or support for charities that support patients, the amount of money donated is insanely small compared with the amounts given to cancer causes.

I have always hated inequality in any sphere of life, and this level of inequality makes me very angry.

Please tell me what will it take to change this picture and make people start to support these lesser known causes that account for far more people.

If the figures don’t count, what will?

Posted in Inequality, Raising MG Awareness | Tagged , , , , , , | 5 Comments

New photo on YESWECAN Team

Hi, just posted this photo on our “YesWeCan” team page

Getting support in Tucson, Arizona, from the local VW club at a special event at Chirco on 31st December 2011. Just look at the weather!!!!

Hoping you can check out our pages from time to time as we’re always adding photos and other updates from the stacks and stacks collected on our drive. It’s just that there’s never enough time in the day, is there?

To keep up to date, please join us on Facebook and Twitter. We have two accounts for each, and the links are shown at the very bottom of each page on this website, so scroll down, down and down again :)

 

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New links: two MG associations in the UK

Today two new links were added to this website.

One is to the Myasthenia Gravis Association (UK)

and the second is to Myasthenic Kids another UK based charity helping children with MG …

… and their families.

Please note links to other MG associations are shown in the links section on this website. You can find them in two places: at the very bottom of every page and blog post; and in the right hand column, as you scroll all the way down past recent posts, comments and categories. Please take a look and check back from time to time to see if we have added more links. ALSO PLEASE TELL US if you know of any MG organisations that you think we should include in this section, by sending us your ideas in the reply/comment box below.

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Have you looked at …..

Have you looked at our updates to the pix page lately?  

We’ve just added this photo of The YesWeCan CamperVan to the page which shows some photos from the trip.

The YesWeCan CamperVan in Carpinteria, California, towards the end of phase 2 of the MG Awareness drive; start date 20 October 2011 from Provincetown, MA, end date 15 May 2012 in Corona, CA, total distance 7853 miles

Before you say it, I admit I am way behind on adding photos from the thousands I took.
I apologize for that, but there’s so much to do every day to raise awareness for MG and other autoimmune diseases.
If you’d like to volunteer by driving your vintage vehicle, helping to administer our website, or our facebook pages and groups, please add your comment on the Volunteer page.

THANKS!!

 

Posted in Raising MG Awareness | Tagged , , | 2 Comments