WOYWW 192............And the winner is........

SIAN!! Many Congratulations to you..... I'd also like to say thank you to everyone who left a comment and said such lovely things about my creations too, It was lovely to read all the positive comments. I'm also pleased to say that the lady who ordered a set in New Jersey received the package today and was delighted with her order too.

If you let me know your address and which set you feel will suit you best then I'll send you it as soon as I can.


In the mean-time... here are some more pieces that I've worked on over the past week...Not at my desk (cos I can't get to it atm ) but mainly sat on or in my bed and I mostly made matching earrings but a couple of new bracelets too...

 Star Spangled Banners





















Autumn Glow

Sunny Daze

Still got the Blues....

















All sets are available to purchase at very agreeable prices too! So please feel free to email me at leelarlou@gmail.com with any queries if you would like to purchase a set.... some of the sets from last week are still available to buy. And last but not least, don't forget to pop onto Julia's place over at Stamping Ground... that's the lady who started off this whole WOYWW!

Lisa
xx

 

WOYWW..... 300 posts!!!..............

Wow! who'd have thought I would have still been blogging for this long?? I try to do crafting whenever I can... scrapbooking, card making, stamping, knitting, crochet, cross-stitch, quilting.... And now I've started to make jewellery and I've even sold a set to a lovely lady across the pond in New Jersey!!

So to celebrate 300 posts I'm giving away some blog candy!!!

I use a combination of semi-precious gem stones, glass beads and seed beads on memory wire and also making earrings to match...

Pink to make the Boys Wink! - SOLD

The Valentine Special

Nature's Glow - SOLD
 















 Melange a Trois - Won by Sian

Blue Lagoon

Putting on the Glitz




















If you would like to own a set of my hand-crafted creations then just leave a comment below & let me know which set you like best.... I'll pick a winner at random & post the winners name the following Wednesday :D

Good Luck and Happy WOYWW

Ooh and of course don't forget to visit Julia at the Stamping Ground

Lisa
xx

I planned on blogging

something Christmassy every day this month.... But today I share the sad news that last night at 19.45 my father passed and is now with my mother again.... my sister A said that his need to be with my mum was greater than his need to be alive.... Mum passed away so suddenly on the 7th March 2007 and Dad just sat waiting to be with her again....
45 years is a long time to be together and we believe he couldn't stand it anymore....

Goodnight and God bless you both Mum and Dad now you are together again.

December 1st....

Happy December everyone, I love Christmas and the run up to it too, getting the tree up and putting presents under the tree too, the kids are old enough now for us to put them there and not pick them up and rattle them!

Anyway, Christmas is coming and so is Mr Wonderful's birthday on the 17th!

ta-ra for now

Lisa

Its nearly the end of the month and I've yet to post anything!!

The last few months have been a bit rough on me healthwise as some of you may know.... but tonight I posted some work on my other blog that I normally use for cards but I have done some work on a little wooden icon that I bought absolutely ages ago..... So on Tuesday (27th) I used some of the great stamps from visible image.

A bit of sad news now tho.... I have had a phone call from my sister tonight saying that my dad is now in hospital and that the doctors expect him to last about a week.... I know it's what he wants tho as he has missed my mum so much over the last 6 years (nearly) and soon they will be together again.

Sending love and kind thoughts to all of you who are going thru similar situations

Lisa
xx

a couple of things I've made lately...

I made this card for the daughter of a friend on Facebook... she was hoping to make her daughters birthday extra special... as it may be her last! I think she got over 400 cards by the time her birthday arrived!

Then I picked up my crochet hook again and some wool, I use Sirdar Calico, mostly because it crochets up nicely but its looks good too. Anyway, there I was crocheting away when Mr Wonderful asks what I was making... "Dunno yet!" says me... Tj said she wanted a beanie!! I was planning on a beret.. so anyway it's a beanieberet! and here it is being modelled by the owner...

This is how I think it should be worn but wearers wear the hat the way the want don't they!!

Thanks for dropping by and ooh today some goodies arrived that I'd ordered to make beads with, now I just have to find a pasta machine to roll out the clay! Bye for now Lisa x

Is it this or is it that?

Dear Human Being,

Hi, my name is Fibromyalgia, and I’m an invisible chronic illness. I am now ‘velcroed’ to you for life. Others around you can’t see me or hear me, but YOUR body feels me. I can attack you anywhere and anyway I please. I can cause severe pain, or if I am in a good mood, I can just cause you to ache all over.

Remember when you and Energy ran around together and had fun? I took Energy from you and gave you Exhaustion. Just try to have fun now! I also took Good Sleep from you and in its place gave you Fibro Fog (a.k.a.) Brain Fog. I can make you tremble internally or make you feel cold or hot when everyone else feels normal. Oh yeah, I can make you feel anxious or depressed, too. If you have something planned, or are looking forward to a great day, I can take that away too. You didn’t ask for me. I chose you for various reasons: that virus you had that you never quite recovered from, or that car accident, or childbirth, ...
the death of a loved one, or maybe it was those years of abuse and trauma. Well, anyway, I’m here to stay! I hear you’re going to see a doctor who can get rid of me. I’m ‘ROFL’ (rolling on the floor laughing)! Just try! You will have to go to many, many doctors until you find one who can help you effectively. In fact, you’ll see many doctors who tell you ‘it’s all in your head’ (or some version of that). If you do find a doctor willing to treat this ‘non-disease’, you will be put on pain pills, sleeping pills, and energy pills. You will be told you are suffering from anxiety or depression, given a TENS unit, told if you just sleep and exercise properly, I will go away. You’ll be told to think positively, poked, prodded, and most of all, you will not be taken seriously when you cry to the doctor how debilitating life is for you every single day!

Your family, friends, and coworkers will all listen to you until they just get tired of hearing about how I make you feel, and that I’m a debilitating disease. Some of them will say things like “Oh, you’re just having a bad day”, or “Well, remember, you can’t expect to do the things you used to do 20 years ago,” not hearing that you said “20 DAYS ago”! Some will just start talking behind your back, while you slowly feel that you are losing your dignity, trying to make them understand, especially when you are in the middle of a conversation with a ‘normal’ person, and can’t remember what you were going to say next!

In closing, you’ve probably figured out that the ONLY place you will get any real support and understanding in dealing with me is with Other People with Fibromyalgia! They are the only ones that will understand your complaints of unrelenting pain, insomnia, fibro fog, the inability to perform the everyday tasks that ‘normal people’ take for granted.

Remember, I’m stuck to you like Velcro – and I expect we’ll be together for the rest of your life.

as written by Lacey 777 

The long and winding road

A few months ago I finally got the courage to go to my GP with my list of ills................ she was great and arranged blood tests and x-rays for my appointment at an out of town hospital... Myself & Husband duly went along to see a really good Doc... after an hour long appointment where we discussed the 2 surveys that we filled out prior to the appointment then Doc says that she cannot confirm that I have CFS/ME due to the many other issues I have that can cause fatigue and pain... ( IBS, Under Active Thyroid, Osteoarthritis in both hips, a couple of prolapsed discs in the lumbar region which of course in turn triggered the Chronic Sciatica... there are quite a few other things too that you all probably have or know of....) So less than two weeks later this letter arrives saying I'm being referred to the sleep clinic because she thinks the reason for the fatigue is sleep apnoea!!! Then this morning I get a call from a lady ringing to arrange an appt for me at a hospital in the Gloucestershire area then.... she realises she has all my details but the name on her screen isn't mine!! but all the other details are ?? She then apologises profusely and laughingly tells me to forget the phone call! on top of that I get a letter in the post from the physio dept telling me to go for physio later this month!! Physio?? It takes me all the time to get up and go downstairs which is why I spend a lot of the day upstairs in our home....Thank goodness for my wonderful wonderful darling husband and great kids and my sister and brother-in-law and my parents-in-law... Oh and my husbands fantastic boss who understands our situation which started off with me going to our the GP and he diagnoses me with a suspected cauda equina lesion/syndrome (he does tell me that he really hopes he's wrong but better be safe than sorry) this is way back in June 2010 and being sent to a local hospital who then refused to do an MRI because they felt it wasn't necessary then me returning back to the then GP still in a heck of a lot of pain, who insisted I have an MRI so arranged one for me on a Sunday morning at another hospital!.... nice understanding staff? Not!! pushed me down and pulled my arms up because and I quote "you're too fat to go thru the MRI so your arms have to go straight above your head..." at this point I realised I was a sufferer of claustrophobia!!! and get all panicky but then succeeded to calm myself down and go thru the MRI which I was told would take 10-15 minutes but it turns out is it more like 35 to 40 minutes..Arms/shoulders very sore and back is feeling so bad I feel faint... anyway this GP then moved on to another surgery and I started to see a lady GP which is the one I have now but she is only available on Thurs & Fridays... the rest of the week its take pot luck if you get one of the other docs who are 4 ladies and 1 gent, Two of the ladies are great, One is absolutely pathetic and puts every illness I have down to my weight... and the Gent doc I've yet to see but my husband took my daughter in for an appt and he was very off with an emotional teenage girl.... so he his on my list of GPs to avoid along with the lady doc previously mentioned.... So, now I guess I am on the long journey of seeing all the different available consultants until someone comes up with the suggestion that was given to me by a friend who is a GP!! Will I finally be diagnosed with CFS/ME or Fibromyalgia? and how many hospitals/clinics can I visit... ha ha ha ha ha ha, gotta keep smiling

:D


L x

Sometimes you see something and you love it straightaway ;-D

http://www.telegraph.co.uk/news/picturegalleries/theweekinpictures/9574584/The-week-in-pictures-28-September-2012.html?frame=2353645

I'm fancying some more masks of late and have spotted some new designs by the talented Ali Reeve.

From top to bottom they are Celtic Border, Choir Border, Elegance Border, Filmstrip Border, Ivy Border and lastly Music Border.... Now the decision is why to get first? after I have gotten the 5 sets of mini masks!!

bye for now

L :-D