Hello, my name is Loretta

[loretta]

New to the forum..thank you to all the replys I received from my fears and questions. I will enjoy reading all your thoughts , laughters, and insights....I will find this forum a great help to what is to come...I am afraid and going through some stages of anxiety. This is only my second week after diagnosis...It has taken me 2 days to read through all the forums pages. I have learned so much more !!!!! Now I will need to learn how to do the photobucket (how?) ????!!!!! I am at the early stage of PD...tremors ( right hand) weakness,lightheadedness, noticeable changes in swallowing (I am finding that I can not swallow like before ) . My eyesight have changed tremendously ! I just retired on July of 07 ...have plans to do lots of rock/gem hunting and I am 64 years old. Have worked for Kaiser Foundation Hosp for 30 years. I have a significant other ( Fred ) for the last 26 years....two wonderful children of 35 and 38 years of age...and 2 grandchildren of 13 and 8 years ( lives in Chicago ) ...
I will take one day at a time and will think positive , and smile and laugh ....I have PD , PD will not have me!!!!!! I will have bad days and hopefully this forum will take me through that time...like today...

When Fred and I are out and about...we may not get any computer/phone line....we are usually in the mountain ranges...

thank you all again...talk to you all again soon !!!

Loretta:)

[heather]

New to the forum..thank you to all the replys I received from my fears and questions. I will enjoy reading all your thoughts , laughters, and insights....I will find this forum a great help to what is to come...I am afraid and going through some stages of anxiety. This is only my second week after diagnosis...It has taken me 2 days to read through all the forums pages. I have learned so much more !!!!! Now I will need to learn how to do the photobucket (how?) ????!!!!! I am at the early stage of PD...tremors ( right hand) weakness,lightheadedness, noticeable changes in swallowing (I am finding that I can not swallow like before ) . My eyesight have changed tremendously ! I just retired on July of 07 ...have plans to do lots of rock/gem hunting and I am 64 years old. Have worked for Kaiser Foundation Hosp for 30 years. I have a significant other ( Fred ) for the last 26 years....two wonderful children of 35 and 38 years of age...and 2 grandchildren of 13 and 8 years ( lives in Chicago ) ...
I will take one day at a time and will think positive , and smile and laugh ....I have PD , PD will not have me!!!!!! I will have bad days and hopefully this forum will take me through that time...like today...

When Fred and I are out and about...we may not get any computer/phone line....we are usually in the mountain ranges...

thank you all again...talk to you all again soon !!!

Loretta:)

Hello Loretta
If you go into hobbies, i have done a section on how to post pictures on hear,if you need any help some one will be willing, as all my pupils:D,:rolleyes:are now experts
There is a lot to read on hear, when some of us joined it was very small, so we found it easy, now even we have difficulty trying to catch up, have you been in the archives at the very bottom of the page, just ask any questions, and someone will answer
Have you seen a speech therapist , they where, a great help for Jim with his swallowing, do you choke when swallowing,if so you may need to thicken, some things, in the UK we have a powder called thick and easy, it thickens but tasteless,have your blood pressure checked, as Jim has low blood pressure, and made him light headed, which was some of the reasons , he would fall
I'm retiring age in a few weeks, but going to go a little longer, i only work 3 days a week 9am-1pm
look forward to seeing pictures
http://i10.photobucket.com/albums/a126/maesisaf/friendbear.jpg

[Drew Saunders]

New to the forum..thank you to all the replys I received from my fears and questions. I will enjoy reading all your thoughts , laughters, and insights....I will find this forum a great help to what is to come...I am afraid and going through some stages of anxiety. This is only my second week after diagnosis...It has taken me 2 days to read through all the forums pages. I have learned so much more !!!!! Now I will need to learn how to do the photobucket (how?) ????!!!!! I am at the early stage of PD...tremors ( right hand) weakness,lightheadedness, noticeable changes in swallowing (I am finding that I can not swallow like before ) . My eyesight have changed tremendously ! I just retired on July of 07 ...have plans to do lots of rock/gem hunting and I am 64 years old. Have worked for Kaiser Foundation Hosp for 30 years. I have a significant other ( Fred ) for the last 26 years....two wonderful children of 35 and 38 years of age...and 2 grandchildren of 13 and 8 years ( lives in Chicago ) ...
I will take one day at a time and will think positive , and smile and laugh ....I have PD , PD will not have me!!!!!! I will have bad days and hopefully this forum will take me through that time...like today...

When Fred and I are out and about...we may not get any computer/phone line....we are usually in the mountain ranges...

thank you all again...talk to you all again soon !!!

Loretta:)

Reference photobucket if you check the archives Heather and I have given instructions on how to do your thing re photos.

[loretta]

Heather and Drew, thank you, I have gone into hobbies and can't seem to find your sections about photobucket....I went to the website and found plenty of photobucket...which one ...no hurry ...I am having a bad day today accepting my diagnosis..I am at the early stages , reason why I and neurologist decided to not go on meds till later. I am reading a lot of info from this forum regarding COQ10...maybe I will try ! Is headpain(backof head), being in a fog,lightheadedness,shoulders and neck pain and heavy palpitations in the chest when resting symptoms of PD? I have an appointment for a second opinion..what questions are important to ask....with PD , we all have different results/progressions...just like all of you, I am very independent and the thought of losing that just kills me. I just took care of my mother who passed away 1 year ago, she was disabled with a severe stroke, but able to live at home with our help till she died...It was hard to see her that way and I do not want to be in that situation....I am not looking forward to this journey!

Allright, Drew, you mention to live each day to the fullest, have laughter , but I cant seem to do that right now....sorry!

there will be better days for me....but not today ....:(

[Drew Saunders]

Heather and Drew, thank you, I have gone into hobbies and can't seem to find your sections about photobucket....I went to the website and found plenty of photobucket...which one ...no hurry ...I am having a bad day today accepting my diagnosis..I am at the early stages , reason why I and neurologist decided to not go on meds till later. I am reading a lot of info from this forum regarding COQ10...maybe I will try ! Is headpain(backof head), being in a fog,lightheadedness,shoulders and neck pain and heavy palpitations in the chest when resting symptoms of PD? I have an appointment for a second opinion..what questions are important to ask....with PD , we all have different results/progressions...just like all of you, I am very independent and the thought of losing that just kills me. I just took care of my mother who passed away 1 year ago, she was disabled with a severe stroke, but able to live at home with our help till she died...It was hard to see her that way and I do not want to be in that situation....I am not looking forward to this journey!

Allright, Drew, you mention to live each day to the fullest, have laughter , but I cant seem to do that right now....sorry!

there will be better days for me....but not today ....:(

I don't know what to say Loretta. We all get blue days as long as every day is not a blue day. If you have a close friend talk to him/her about how you feel. A problem shared....... it may help. Do not think too far ahead. I will think about what you have written and come back with something positive. Just need time for formulate things in my mind.
Have the best day you can,
Drew

[suzie Q]

Hi Again Loretta


Your allowed to feel like that it is not fair that we have this disease,but dont let it ruin your life.no one knows what the future holds,not just us with parkinson's but everybody.at least we have something that is not a death sentence,Don't dwell on what might happen because it might not .I was 48when diagnosed I am 53 now and i am much better now than then .It effects everyone differently,and i am sure attitude has a lot to do with it.I started on the traditional parkinson meds but at the moment i am having great sucess with Mucuna Pruriens (without any side effects).If you look up my profile and look at all the posts i have posted you will find where i talked about it .If not let me know I will find it for you

i hope that you are feeling a little better .talk soon

Sue

[loretta]

I don't know what to say Loretta. We all get blue days as long as every day is not a blue day. If you have a close friend talk to him/her about how you feel. A problem shared....... it may help. Do not think too far ahead. I will think about what you have written and come back with something positive. Just need time for formulate things in my mind.
Have the best day you can,
Drew

Thank you, Drew, I am having a better day today ! Woke up feeling good about myself...and will be going out to do shop shopping !:)

[loretta]

Hi Again Loretta


Your allowed to feel like that it is not fair that we have this disease,but dont let it ruin your life.no one knows what the future holds,not just us with parkinson's but everybody.at least we have something that is not a death sentence,Don't dwell on what might happen because it might not .I was 48when diagnosed I am 53 now and i am much better now than then .It effects everyone differently,and i am sure attitude has a lot to do with it.I started on the traditional parkinson meds but at the moment i am having great sucess with Mucuna Pruriens (without any side effects).If you look up my profile and look at all the posts i have posted you will find where i talked about it .If not let me know I will find it for you

i hope that you are feeling a little better .talk soon

Sue
Hi, Sue, feeling better today! Woke up feeling good about myself ...will be going out to go shopping today! I am taking notes about all the things in this forum....will keep Mucuna Pruriens in mind when I see the dr. again...that is what I am afraid of ( I think ) are the side effects of meds... please send me the info ...thank you :)

[ltd-addition]

Hi Loretta

Well my little spring Chick, never fear (limited) ltd is here, I'm one of the forums additions !
I'm a young Gazelle with Parker's, dancing along in my red tutu & high heeled shoes wearing my purple hat !

I'm totally & utterly sane on occasions

I understand your concerns regarding your future.
Did you know depression is 1 of the symptoms of Parker's, I must have been swinging off the chandelier prior to pd. I have a 6 yr old son who is a gift from heaven and my Husband who is my soul mate.

Girl you are in turmoil with yourself but it's understandable , 1 step at a time or else you'll fall off your high heel's.

You can't turn the clock back but it doesn't mean you have to take the battery out to make it stop.

Iv'e got young onset Parkers having been diagnosed prior to 40yrs of age. 6 yrs on at 45yrs i'm still working full time , run 2 little hobby businesses of selling jewellery & floral arrangements, run a home & care for my family.

Up until 2 yrs ago I was doing bank nursing on my day's off to keep my nursing registration up.

For the last 6 yrs I've been having diffuculties with my present employer but very recently I've had to liaise with my union solicitor whilst dealing with an internal grievance procedure in order to keep my job. Plus getting moved to temporary job from temporary job.

Sept 07 I was diagnosed with dyscalculia a form of dylexia with numbers

In February 08 i was misdiagnosed with cancer and on April 25th operated on for a rare condition. I'm waiting for another op if the 1st hasn't worked.

But Loretta you know who has been the understanding support for me apart from my friends & family. This forum yes, my respect for my friends Drew his wife Elaine, Heather formally known to me as My Angel with her halo sque whif (slipping off he he ) Margie my spring bottle of red shiraz from New York, Susan my lake district , Sue my Aussie friend aka suzie q, pogo, filo1960,Canadian club , Tinkerbell my fairy, gail, bunny, Bruce, Heather p & everyone else on this forum.

I reckon you go with the flow and do whatever floats your boat.
I'm not courageous or special but I know the folk on this forum care enough to make me feel I am.
faith , hope and charity was written to describe us with Parkers & the carer's.
Faith in each other
Hope we don't fall too far off our high heeled shoes, unless its alcohol related ! whilst waiting for our cure.
Charity because they'd give their last breath to assist anyone.

We are lucky for knowing we have each and every one of us who understand & give guidance , strength & laughter.
Now your depressed about my life you forgot how bad your feeling ha ha I knew I'd make you feel lucky !
Keep smiling

[Drew Saunders]

Thank you, Drew, I am having a better day today ! Woke up feeling good about myself...and will be going out to do shop shopping !:)

Hi Loretta,
My wife Elaine and I have been discussing your problem i.e. the shock and realisation of what you have. Let's not kid ourselves - shock horror - nobody knows what causes this and for the moment nobody has a cure but watch this space.
There are 2 ways to approach this problem.
1. Give in and feel sorry for yourself - go into denial and take no meds. Fine, NOT, your life will be a misery and is this what you want? I don't think so.
2. Be positive. Fight Parkies. You can win - really you can. Take advice from the medical fratenity as long as it is positive. If they come over negative go for a second opinion. This may be difficult to get your head around but a positive attitude works wonders.
No person has ever died from Parkies only with it. So that is a good start, Yeh?
Depending how Parkies affects you there are meds out there to help you. All you need is meds to help you counteract how it affects your body now. Trial and error to get the meds right for you. The future? Let that sort itself out. If you worry how you may be in the future puts huge pressure on you and that is the last thing you need. It will only accelerate your condition so forget it.
If and when something else kicks in then take more advice and deal with it. Back to trial and error on meds to deal with the new problem.
Situations to avoid:-
STRESS/ANXIETY. Below the belt blows. Avoid at all costs. Your symptoms will only worsen and accelarate your down turn. Life is too short for this.
THE FUTURE. You can drive yourself crazy thinking about how you are going to be in the future or what is round the corner. Live for today - period!
DEPRESSION. Very common in Parkies. If it swamps you get meds to cope. If you do not then symptoms get worse.
Now the sunny side:-
HUMOUR. Essential. Where ever you are and whatever you're doing see the funny side of life. Try and be in the company of people who make you smile/giggle/laugh. Very important. Don't know anybody like that? I'm sure there is a programme on TV that will and try and share it with someone. Makes it infective laughing with someone.
MEDS. Medication not working? Talk to a medic you trust and increase/change meds to make your quality of life better.
THIS FORUM. I know you are new to the forum so if you want to look back to what has been said on a given subject check out the small heading with numbers i.e "1,2,3,4 latest". If there is something of interest for you then you can reply to that imput and hopefully get feed back.
Heather is the expert on getting photos onto the forum. Contact her directly and she will be able to give you advice on inputing such on the forum.
I do hope that my ramblings have been helpful to you but if you have any questions please do hesitate to ask - anytime.
Have the best day that you can,
Drew

[Drew Saunders]

Hi Loretta

Well my little spring Chick, never fear (limited) ltd is here, I'm one of the forums additions !
I'm a young Gazelle with Parker's, dancing along in my red tutu & high heeled shoes wearing my purple hat !

I'm totally & utterly sane on occasions

I understand your concerns regarding your future.
Did you know depression is 1 of the symptoms of Parker's, I must have been swinging off the chandelier prior to pd. I have a 6 yr old son who is a gift from heaven and my Husband who is my soul mate.

Girl you are in turmoil with yourself but it's understandable , 1 step at a time or else you'll fall off your high heel's.

You can't turn the clock back but it doesn't mean you have to take the battery out to make it stop.

Iv'e got young onset Parkers having been diagnosed prior to 40yrs of age. 6 yrs on at 45yrs i'm still working full time , run 2 little hobby businesses of selling jewellery & floral arrangements, run a home & care for my family.

Up until 2 yrs ago I was doing bank nursing on my day's off to keep my nursing registration up.

For the last 6 yrs I've been having diffuculties with my present employer but very recently I've had to liaise with my union solicitor whilst dealing with an internal grievance procedure in order to keep my job. Plus getting moved to temporary job from temporary job.

Sept 07 I was diagnosed with dyscalculia a form of dylexia with numbers

In February 08 i was misdiagnosed with cancer and on April 25th operated on for a rare condition. I'm waiting for another op if the 1st hasn't worked.

But Loretta you know who has been the understanding support for me apart from my friends & family. This forum yes, my respect for my friends Drew his wife Elaine, Heather formally known to me as My Angel with her halo sque whif (slipping off he he ) Margie my spring bottle of red shiraz from New York, Susan my lake district , Sue my Aussie friend aka suzie q, pogo1960, Tinkerbell my fairy, gail, bunny, Bruce, Heather p & everyone else on this forum.

I reckon you go with the flow and do whatever floats your boat.
I'm not courageous or special but I know the folk on this forum care enough to make me feel I am.
faith , hope and charity was written to describe us with Parkers & the carer's.
Faith in each other
Hope we don't fall too far off our high heeled shoes, unless its alcohol related ! whilst waiting for our cure.
Charity because they'd give their last breath to assist anyone.

We are lucky for knowing we have each and every one of us who understand & give guidance , strength & laughter.
Now your depressed about my life you forgot how bad your feeling ha ha I knew I'd make you feel lucky !
Keep smiling

Don't you believe it - she's as mad as a fish!!! Thank goodness, without ltd (there are no others like her!) the world would be a very dull place. Take on board what she says she is not as daft as she sounds! Believe me, i know.

[loretta]

Hi Loretta

Well my little spring Chick, never fear (limited) ltd is here, I'm one of the forums additions !
I'm a young Gazelle with Parker's, dancing along in my red tutu & high heeled shoes wearing my purple hat !

I'm totally & utterly sane on occasions

I understand your concerns regarding your future.
Did you know depression is 1 of the symptoms of Parker's, I must have been swinging off the chandelier prior to pd. I have a 6 yr old son who is a gift from heaven and my Husband who is my soul mate.

Girl you are in turmoil with yourself but it's understandable , 1 step at a time or else you'll fall off your high heel's.

You can't turn the clock back but it doesn't mean you have to take the battery out to make it stop.

Iv'e got young onset Parkers having been diagnosed prior to 40yrs of age. 6 yrs on at 45yrs i'm still working full time , run 2 little hobby businesses of selling jewellery & floral arrangements, run a home & care for my family.

Up until 2 yrs ago I was doing bank nursing on my day's off to keep my nursing registration up.

For the last 6 yrs I've been having diffuculties with my present employer but very recently I've had to liaise with my union solicitor whilst dealing with an internal grievance procedure in order to keep my job. Plus getting moved to temporary job from temporary job.

Sept 07 I was diagnosed with dyscalculia a form of dylexia with numbers

In February 08 i was misdiagnosed with cancer and on April 25th operated on for a rare condition. I'm waiting for another op if the 1st hasn't worked.

But Loretta you know who has been the understanding support for me apart from my friends & family. This forum yes, my respect for my friends Drew his wife Elaine, Heather formally known to me as My Angel with her halo sque whif (slipping off he he ) Margie my spring bottle of red shiraz from New York, Susan my lake district , Sue my Aussie friend aka suzie q, pogo1960, Tinkerbell my fairy, gail, bunny, Bruce, Heather p & everyone else on this forum.

I reckon you go with the flow and do whatever floats your boat.
I'm not courageous or special but I know the folk on this forum care enough to make me feel I am.
faith , hope and charity was written to describe us with Parkers & the carer's.
Faith in each other
Hope we don't fall too far off our high heeled shoes, unless its alcohol related ! whilst waiting for our cure.
Charity because they'd give their last breath to assist anyone.

We are lucky for knowing we have each and every one of us who understand & give guidance , strength & laughter.
Now your depressed about my life you forgot how bad your feeling ha ha I knew I'd make you feel lucky !
Keep smiling

Hi, ltd-addition

My mind is whirling trying to imagine your red tutu,purple hat and high heel shoes ( red,too?). Your right, by the time I finished reading your note, I was in tears, and I just can't imagine all those things happening to you. I know that I am going to have lots of friends in this forum...you and others will carry me through this and hopefully I can do the same for you and others. Yesterday, I was feeling really down, but today I am ok and almost my old self....everyone in this forum is remarkable! The laughter and care that comes across...is phenomenal ! I will have bad and good days ( more of good , I hope),family / friends and the " forum " will guide me.Now if I can only learn how to do the "photobucket"....yuck!!!!!!

I have two children 38 (girl)and 35(boy) years old...2
grandchildren 13(girl) and 7(boy) years old .Grandkids live in Chicago. I have a significant other of 26 years, retired last year
after 30 years, was planning to work parttime this summer, now I don't know if anyone will hire me ! Fred and I like to travel and go rock/gem hunting...so we will till I can't ! Ill bet your jewelry and floral arrangements are beautiful !

Hope all goes well with you...so no more surgery ! Your 6 year old must keep you and your husband busy !

Thank You for lifting my spirits up....ltd-addition!

Loretta:)

[loretta]

Hi Loretta,
My wife Elaine and I have been discussing your problem i.e. the shock and realisation of what you have. Let's not kid ourselves - shock horror - nobody knows what causes this and for the moment nobody has a cure but watch this space.
There are 2 ways to approach this problem.
1. Give in and feel sorry for yourself - go into denial and take no meds. Fine, NOT, your life will be a misery and is this what you want? I don't think so.
2. Be positive. Fight Parkies. You can win - really you can. Take advice from the medical fratenity as long as it is positive. If they come over negative go for a second opinion. This may be difficult to get your head around but a positive attitude works wonders.
No person has ever died from Parkies only with it. So that is a good start, Yeh?
Depending how Parkies affects you there are meds out there to help you. All you need is meds to help you counteract how it affects your body now. Trial and error to get the meds right for you. The future? Let that sort itself out. If you worry how you may be in the future puts huge pressure on you and that is the last thing you need. It will only accelerate your condition so forget it.
If and when something else kicks in then take more advice and deal with it. Back to trial and error on meds to deal with the new problem.
Situations to avoid:-
STRESS/ANXIETY. Below the belt blows. Avoid at all costs. Your symptoms will only worsen and accelarate your down turn. Life is too short for this.
THE FUTURE. You can drive yourself crazy thinking about how you are going to be in the future or what is round the corner. Live for today - period!
DEPRESSION. Very common in Parkies. If it swamps you get meds to cope. If you do not then symptoms get worse.
Now the sunny side:-
HUMOUR. Essential. Where ever you are and whatever you're doing see the funny side of life. Try and be in the company of people who make you smile/giggle/laugh. Very important. Don't know anybody like that? I'm sure there is a programme on TV that will and try and share it with someone. Makes it infective laughing with someone.
MEDS. Medication not working? Talk to a medic you trust and increase/change meds to make your quality of life better.
THIS FORUM. I know you are new to the forum so if you want to look back to what has been said on a given subject check out the small heading with numbers i.e "1,2,3,4 latest". If there is something of interest for you then you can reply to that imput and hopefully get feed back.
Heather is the expert on getting photos onto the forum. Contact her directly and she will be able to give you advice on inputing such on the forum.
I do hope that my ramblings have been helpful to you but if you have any questions please do hesitate to ask - anytime.
Have the best day that you can,
Drew

Shock Horror is correct !!!! Thank you Elaine and Drew ! My kids and Fred are trying to keep me on track ,too. You are right, I cannot let this take me down....whenever I am feeling low , I will read your note to let me know I am not alone ...

I think I have read all the" Forum "pages and info ....I think my brain is on "overload" ! and I agree, that surfing the web was too much....

Wow, ltd-addition - what can I say....she lifted my spirits!!! Everyone has so many nice things to say .

To all the good days to come!
Loretta

[Gail]

Loretta, Glad to here you are having a better day. The bad days will come and go, but it can't be stressed enough that a poitive attitude is the most important thing. When you are having a bad day, as we all do, this group can help you through it. They will let you vent, acknowledge that you have a right to feel the way you do, and then offer you their collective wisdom and insightful advice. If that doesn't get you moving in the right direction, they offer you chocolate. Where else can you get free advice and chocolate?

[ltd-addition]

Loretta, Glad to here you are having a better day. The bad days will come and go, but it can't be stressed enough that a poitive attitude is the most important thing. When you are having a bad day, as we all do, this group can help you through it. They will let you vent, acknowledge that you have a right to feel the way you do, and then offer you their collective wisdom and insightful advice. If that doesn't get you moving in the right direction, they offer you chocolate. Where else can you get free advice and chocolate?

Ha ha Gail well said, oops I just dropped my chocolate dunking it too long in my tea!

[Gail]

Ha ha Gail well said, oops I just dropped my chocolate dunking it too long in my tea!Was there Baleys in the tea or is that only for coffee?

[heather]

Hi Loretta
So Glad you are feeling, more positive
welcome to the club, we are a strong club, no one wants to be in it, but we are signed up for life

I am a carer for Jim for 12 +years [age 54] and his scan showed many years before ,who has a illness that mimics PD, so i only comment as a carer, or anything i have learnt on hear off my PD friends
Drew said a very important thing, which i hope if you remember nothing else you remember this

NO ONE DIES OF PD
This is so true, 12 years ago they gave Jim 7 Years , so i asked his neurologist since when have you been god
3 years ago this Christmas, he told me to take Jim home and enjoy your last Christmas, so having a gob I replied "see you are still practising being God" he was not amused, but then nether was I
After 7 years i/we could have said that's it but i'm the kind of person that says if you say i can't i will [ even cut my nose off to spite my face]
I have brought out the Archives how to get around the site, and also posting pictures , you will so enjoy posting them, and we all have a laugh doing it, if you need help please say, we can do it on hear or through e-mail, I have to say i have dyslexia, but my friends say they can understand it
If you can't see the pictures already posted, with out clicking on the link, then you need to do the part above the red line

As promised
instructions to post pictures on site

To see pictures on site

FIRST GO INTO USER C.P, [TOP LEFT HAND CORNER ]
CLICK ON EDIT OPTIONS , THEN
THREAD DISPLAY OPTIONS


Visible Post Elements

Show Signatures
Show Avatars
Show Images (including attached images and images in [IMG] code)
TICKTHIS BOX
-----------------------------------------------------------

TO POST PICTURES
please excuse me if it sounds like i'm talking to a child,but i don't no how much everyone knows about computers

There are a few very important rules before posting pictures,which you should read when joining

A. Nothing that resembles Porn

B. Nothing that is offensive or racist

C.If copying anyone's work and is water market with their name etc, make sure that this is not removed. as this acknowledges,it's someone else's work not yours. and you can be trace,

D. Out of politeness I personally,always say when i have copied, by saying Thank you SNAGGED,this is only me,and not necessary

Anything I post is free to take,and don't need a thank you, just enjoy.

Equipment needed

1. make a new folder on your desktop [ right click on mouse, on desk top Click on folder go down to New,and click on first one ] and name it.
[mine named "my pictures" ]

2. need to down load a Image hosting, the one below i use it's FREE and easy

2a Image hosting, free photo sharing & video sharing at Photobucket

www.photobucket.com/


now to start

1.b. http://www.uselessgraphics.com/ [Lot's pictures to start you off ]
find a picture ,right click on mouse,click on"save as " [if this doesn't come up in the list then it has copy rights and you can't copy it]

it will ask you where you want to save it
it may say the name of your folder,or you may have to click on drop down, click on "desk top" look for your folder, click on it, and then on save .

open Photobucket or what ever imaging host you use,i have done this using photobucket

1.Click on brows,it will open in your folder, find picture [one short click will turn all around blue] click open.

you will automatically go back to brows click on UPLOAD

it will take a little time to load ,a bar will come up say how much loaded once 100% ,after a few seconds you will see your picture [Almost finished ]

2. at the bottom you will see [image code] click on this and it will say copied

3.go to your post on hear
Right click
click on paste



and that's it

always save a picture, GIF or JPEG
any problems just ask,ohhhh and don't forget to excuse the spelling
Have fun
__________________


Take care and keep :D:)

[MargieA]

Was there Baleys in the tea or is that only for coffee?

I didn't know you could Baileys in tea and/or coffee! My 'lesson' for today...ha! ha!

Hope you are having a good day. Margie :)

[MargieA]

Ha ha Gail well said, oops I just dropped my chocolate dunking it too long in my tea!

Hi ltd_addition - Next cup of tea you plan to dunk your chocolate in...my secret...have a reserve piece of chocolate in your napkin (hee! hee!) Or you could try this http://i302.photobucket.com/albums/nn88/Bronx628Margie/Chocolatetea001.jpg

Oh, we're a clever bunch! Margie:)

[Gail]

I didn't know you could Baileys in tea and/or coffee! My 'lesson' for today...ha! ha!

Hope you are having a good day. Margie :)Baileys is great in coffee. Not sure what it would do to tea.