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If you're an oldie and have not yet
posted an introduction, now's the time! lol. Our newbies have an easier time
of it when they can learn just a little about us before diving into the
posting. Will you click here to leave us your introduction?
To Post your
Introduction, please
click here.
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Introductions
Sleepyhead: Hiya I'm sleepyhead,
aka Kirsty. I'm 21 and live in
Birmingham, but also spend a lot of time
in Telford with my boyfriend. I've had
M.E for 6 years now. I'm about to start
my final year at University of a Primary
Education degree to become a teacher!
I'm really looking forward to getting to
know you all.
mbali12: Hey everyone I am
Natalie (you can call me Nat) I am 22
yrs old and I was diagnosed with M.E and
fibro 2 years ago but like a lot of
people I believe I have had the both a
lot longer dating back to when I was 14
yrs old but one doctor said I was just a
lazy teenager and that I should get my
act together and stop pretending...I
might add I know longer see this
doctor!!! I live with my mum, older
sister and her 2 children my niece and
nephew and my older brother...oh yeah
and not forgetting my two gorgeous cats
Marley and Tinkerbelle. I am engaged to
a lovely man called Mark we have been
together for 2 years, we had only been
together for 9 months when I became
really ill and it felt like over night I
became very dependent on him. We had
loads of chats and I told him I would
understand if he know longer wanted to
be with me but luckily he said know way
I am going to stay with you and fight
this together. He works full time and
lives in his own flat but he is main
carer as he comes round every night
straight from work and helps me with
things like if I want a shower or I have
got one of them annoying forms from the
benefits!! He never goes home until he
see's me taking my night time tablets!!
My sister looks after me during the day
but she is also very busy as she is our
mum's full time carer and she has also
got a 11 year old daughter and a 10
month old son. I have to use a crutch to
help me get around the house and when I
get the odd chance of going out I use y
top of the range wheelchair!! I have
decorated them both with leopard print
material...I still need to look stylish.
Before I was ill I was very active, I
lead an art and drama group for children
in care and I also went into secondary
schools delivering acting, singing and
art workshops all to do with different
issues the young people might face. I
also started to do some professional
acting with a local small theatre group
touring around the local primary schools
doing 4 short Theatre In Education plays
and workshops in conjunction with the
NSPCC. I also met my fiancé at a amdram
musical theatre drama society, we played
boyfriend and girlfriend in the panto!!!
One day I hope that I will be able to go
back on the stage as this is all in know
I have been doing it since I was 9 years
old and it has given me some many
experiences and opportunities, when I
was 16yrs old I went over to South
Africa for a month with a drama group I
belonged to and we performed with
students from the market theatre in
jo'burg and then the year after I
performed in Poland.
silver2529: Not good at these
intro things, but in time I hope to get
to know you better through the boards!
Here is a bit about me: 28, from USA,
interests: my cat, beading, visual
communication, drumming4 health& self
expression. CFS: diagnosed in 2002, It
came out of nowhere& changed my life
completely!
--___--AngeL--___--1 Hi I'm
Yvonne. I live in Reading with my
husband Phil. We got married on the 26th
July this year and our day was
brilliant. I suffer from Fibromyalgia,
M.E. Degenerative Discs n Faucets,
Osteoarthritis, IBS n Hypoglycemia
Migraines. I am a full time carer to my
fiancé Phil who is a full time
wheelchair user thanks to Friedreich's
Ataxia. My daughter Elizabeth (Lizzie) n
Lizzie's boyfriend Danny, my son Paul is
n his girlfriend Manda are all at uni in
Derby. I also have a daughter called
Yvonne (Vonnie), she lives with my
lovely grandson Jordan whose 2, 3 at the
end of September. Everyday life is a
struggle but we always manage to get
through it (although I don't know how at
times). Phil is my soul mate, he is
always there for me. He has turned my
life around n swept me off my feet at
our wedding. Although he can't walk, he
helps in other ways. He makes me laugh n
smile n is always there to sort out any
probs. I love him very much. This is a
fantastic group, full of support for
every1, there will always be some1 who
can help if you have a prob. This is a
very friendly group. It is an honour to
be part of this group. Newbies plz don't
be shy come n say hello to every1. Plz
take care. Gentle huggies to you all.
Angel xx
☆☆☆
Member of the Month!
Click here to help the
Management congratulate Jasminola!
☆☆☆
Trivia Champion!
Congratulations
Jasmine!
Page Two
Newsletter Archives
To
M.E. or not to M.E. Preview
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New Members in August
Branflaked1
cmrtaman07
Dylan-Paul
LOU
madchatterjo
mbali12
silver2529
sleepyhead
stewiii0
villawend
☆☆☆
Birthdays
September 4: Mellie
☆☆☆
Anniversaries
September 10: Helen
September 19: Steve and Cath
September 24: Clare and Dave
☆☆☆
August in Review
Angel: Hi Every1,
Well it was a very busy month for Phil & myself. We came back from our honeymoon
on the 3rd August and we had a wonderful time. We took 2 carers with us and for
the 1st time in over 5 years I had a complete break. I could swim in the hotel
swimming pool, go shopping, sleep when I needed to & even go to the pub LOL. I
came back totally refreshed and recharged. While we were away on our honeymoon
the carers, Phil and I sorted out about them both being private carers for us
and moving in. We knew the carers well, had even partied with some of their
friends, and their friends who took us in as their own family even came to the
wedding which did add to making our day extra special. Its been hectic since we
got back, the carers resigned from GP Homecare. But... all the good carers are
leaving, as the office staff have no idea how to run the company and expect
their to work 16 hours a day. The day after we got back GP Homecare cancelled
all of Phil's calls and it was Damian that stepped in and said he would do the
calls for Phil even thou he was working at the hospital. Today Damian and Agnes
have moved in
and Agnes has gone back to Poland and Damian will be following her next
Thursday. They come back on the 13th September and will be starting straight
away. In the meantime we have a fantastic carer called Marcella, the 1st time
she came in to help with Phil she got the routine straight away and we've never
had any probs. Marcella will be coming everyday to see to Phil while Damian &
Agnes are away. That is when I get my life back and I can take care of myself
better by being able to attend appointments etc. We've been busy collecting all
the videos and piccies from the wedding so Phil's cousin Dave can put it on to
DVD for us. So if you all would like 1 plz email me on
Ill_be_your_angel@hotmail.co.uk with your home address and as soon as they are
done I will send them out to you.
Our
thoughts and prayers are with Shell. Her mom was diagnosed with
breast cancer this month, underwent a lumpectomy and is now waiting results of
the biopsy of her lymph glands. Hugs, Shell!
Our thoughts and prayers are also with Allie as she walks through the
same journey with her friend.
Teri: Well, at 56 years
old, I went back to school this month. Wow! It not like going to
school when you're young! lol. I have been to massage school before and
attained a license to practice but let that license lapse when I decided to stay
home and home school my kids. Getting it back is sooooo much more
difficult than it would have been to keep it! However, I'm learning lots
of new things and I'll be a much better therapist for it. I'm also working
on attaining my Masters in Reiki. What this means is that I've barely time
to breath. I'm excited about what I'm learning though and that keeps me
going.......... well.... that and the thought that I only have to live in this
pressure cooker for a year lol.
☆☆☆
Introductions Continued..............
UnweariedStevie: Hi all, I am
Steve, 47, male, good lookin, married
with 2 kids. In Full time employment
even over the 11 years I have had ME.
Triggered by Chicken pox, glandular
fever and Pneumonia I am much improved
by being positive and trying several
therapies and supplements.
I was one of the original founders of
this group helping to set it up but had
to bow out gracefully due to increasing
commitments to my business
www.kontrolsports.co.uk which is doing
very well... recent page rank of 3! and
hoping to give up the fulltime day job
soon to take the business further.
☆☆☆
Article of the Month
Drugs versus
Nutritional Medicine for Common Health Complaints
by Jerome Burne (more
info)
listed in nutrition, originally published in issue 134 - April 2007
These days we are all pretty
sophisticated about the gap between rhetoric and reality. Our detectors are
finely tuned when it comes to sniffing out the hype in adverts or the promises
of political parties, but they all-too-often become curiously disconnected when
faced with claims about the benefits of drugs. Maybe it’s because drugs offer a
quick fix when we are at our most vulnerable that we yearn to believe they are
somehow not so tainted with the hucksterism of the marketplace as, say,
double-glazing or life insurance.
Click here for the rest of the article:
☆☆☆
Remember, From M.E.
to You has become a collaborative effort. With
Teri's school schedule she just isn't able to write 3 to 5
pages anymore. If any of you would like to contribute
to our newsletter, please e-mail Teri or sign up on the
Newsletter Message Board. Thanks!
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