PDA

View Full Version : Hello all newbies



Angel Oliver
01-27-2011, 02:15 AM
I would just like to welcome all the newcomers as i have noticed i keep missing some of you.So glad you are here,just wish under better circumstances,but you have found a great forum full of kind and caring,supportivve members.Sorry if i missed you...bit stop by n say hi if you want too....or keep posting as everyone will always reply.Ask us any questions,one of us or all of us will understand whats going on.
Lots of love
Amanda.xxxx

Matildajo
01-27-2011, 06:27 AM
Thanks Angel, glad I found the site. No one understands except those who live it.

rob
01-27-2011, 11:15 AM
Thanks Angel, glad I found the site. No one understands except those who live it.

Welcome to our group Matildajo. Please make yourself at home!

Rob

Peridot_Gem
01-27-2011, 01:00 PM
Hello Matildajo,
Welcome to the WHL and we're all here to support one another, there's so many threads for you to venture through for understanding the Disease more and it will be nice getting to know you.

Terri xxx

Peridot_Gem
01-27-2011, 01:01 PM
I would just like to welcome all the newcomers as i have noticed i keep missing some of you.So glad you are here,just wish under better circumstances,but you have found a great forum full of kind and caring,supportivve members.Sorry if i missed you...bit stop by n say hi if you want too....or keep posting as everyone will always reply.Ask us any questions,one of us or all of us will understand whats going on.
Lots of love
Amanda.xxxxHi Amanda,

Nice post mate for all new comers and i hope your keeping fine.

Terri xxx

Angel Oliver
01-27-2011, 01:14 PM
Hi Matildajo, you are so right!! Let us know about yourself or ask us anything,et us see if we can make a difference.This place help me so much.

Hi Terri how are you feeling today,i hope a little easier. Im just getting over pleurisy so feel like an old ship, creeky rib cage,aches n pains,but im ok thanks.Been to the doctors,lol wait till you read it lol i'll do another thread...funny.

P.s i know my spelling is bad,either typing to fast,meds or just plain bad spelling lol....sorry.xx

Lots of love.
Amanda.xxxxxx

Shining Star
01-27-2011, 06:29 PM
Apparently, it says I am not so newbie now! But thanks for the hello anyway.... how is the pleurisy today? The trouble with lupus (hey, a novel could be written with that beginning) is that it ebbs and flows like a frustrating and teasing sea sometimes. And the doctors seem to meet you right at the point of the ebb... or do I mean flow?!!
Good wishes right back at you x

http://shaistatayabali.blogspot.com/

rob
01-27-2011, 06:55 PM
The trouble with lupus (hey, a novel could be written with that beginning) is that it ebbs and flows like a frustrating and teasing sea sometimes. And the doctors seem to meet you right at the point of the ebb... or do I mean flow?!!
http://shaistatayabali.blogspot.com/

I've never heard the trials and tribulations of being diagnosed with, and then living with Lupus, put into such poetic words.

Well said,

Rob

Saysusie
01-27-2011, 10:09 PM
I would also like to add my welcome to all of our newbies, and not so newbies, as I seem to miss some of you also.
Thank you, Angel, for starting this thread :-)

Peace and Blessings
Namaste
Saysusie

Angel Oliver
01-28-2011, 05:49 AM
Lovely words,i understood you ebbs away was enough lol at my soul lol.Today im sounding like a wheezy dirty old man lol,so the medicine is working.Today is not as bad thanks.I hope your day is a good one.Welcome not so newbie Shining Star thanks for asking.

Thanks Saysusie, used to be one but was a bit old so did a new one as i can not always post to them all.Rusty fingers with a hint of numbness lol.Hope you are having a nice day,always in my thoughts.

I see more new people have joined....sorry i can not post to all, but know i see you there,here so welcome.

love n hugs
Amanda.xxxx

tgal
01-28-2011, 09:34 AM
I too wanted to stop in and add my welcome to all of those that have just joined us or those that are reading but haven't signed up (yet). Please know that this site and all of the people here understand what you are going through and we are so glad to have more members of our WHL family

Angel Oliver
01-30-2011, 04:22 PM
I see we have a few new more members here,so im sending out a big hello and welcome to you all,as ive not posted on all the threads.Hope to chat with you soon.

lots of love
Amanda.xxxx

Angel Oliver
02-01-2011, 12:50 AM
I am so happy to see the new members here posting more often.Just know we truly care and are here to answer anything no matter how small.I see some of you have just been diagnosed which is a scary time at first so many questions.Please dont ever be afraid to ask or tell us your story.We are also here to make new friends and hear about your life.Some of us d not get out that often or have insomnia so are online what seems allot of hours in the day.Then suddeley we dissapear due to anxiety,pain,depression or life in general,but we always come back.Family are not always as understanding,for me talking to people outside my family circle and not to my friends who know me,because they sometimes,ok allot of time just dont get it.But after many months even years of an illness,people get bored of listening to the same story,as in their eyes we never get better.lol.Well sometimes its an uphill struggle and its good to chat here.Hope we can help if only a little.
Lots of love n hugs
Amanda.xxxx

lovehubby
02-01-2011, 09:24 PM
Hi I am new to this and i am not sue what I am doing. But I have Lupus they say. I would like to think they are wrong but I hurt to much in my joints so something is wrong. Sun makes me sick gives me bad headaches. My ana and my ds-dna are positive so my dr, saids lupus. I get rashes really easy too. Well was soon as I can except this think the better I will be I hope Thanks for listening

Peridot_Gem
02-02-2011, 07:13 AM
Hi I am new to this and i am not sue what I am doing. But I have Lupus they say. I would like to think they are wrong but I hurt to much in my joints so something is wrong. Sun makes me sick gives me bad headaches. My ana and my ds-dna are positive so my dr, saids lupus. I get rashes really easy too. Well was soon as I can except this think the better I will be I hope Thanks for listeningHi Michele,
Welcome again and just add to post that you read and feel you need to respond to as all info helps one another on here, as we learn something new everyday.
If the readings have come in saying you have Lupus they would'nt have said otherwise, as it causes your bloods to fluctuate so much it's unbelieveable. If the sun hurts that much like it does me, use a 50 block to protect your skin and i can only go out for 10mins when the summer hits we and that as to be in the shade, please don't hurt your skin as that's the worst thing you can do besides it can cause rashes.
Your doctor saying your ana and dna are positive also, as i'm the same with my ana and ena and that's my autoimmune disease, which you may have also, i would ask them if you have that as well.

Wheather you except it is another matter and alot of members have managed to live their lives around it and some find it hard i'm one who finds it a struggle but we all do things differentley concerning illness.

It will be nice getting to know and and you definitley have people and friends who understand what you going through.

Love Terri xxx

Angel Oliver
03-14-2011, 02:49 PM
Hi Michele sorry its taken a while for me to get here but i see Terri helped you out.I am sorry to all the newbies,but sometimes i dont get on here ,doesnt mean i dont care.Im feeling a bit low,so i hide or play games online while i think things through.So welcome to all of you who are joining.
Lots of love
Amanda.xxxx