I am 42 with sle and heart and lung diseases just looking for new friends

[Enya2010]

I am 42 I have sle lupus and heart and lung diseases I'm on a convocation of drugs. I'm looking for new friends to bond with for advice and support and to be a support to others too.

[NeuronerdDoaty]

Hello and welcome 🙋‍♀️💐

[Enya2010 in reply to NeuronerdDoaty]

Thank you xx

[Careful1]

Hello 🙋

[Enya2010 in reply to Careful1]

Hi thank you for replying x

[thestorm]

Hi Enya, and We are glad you found this site! Everyone here is very helpful and caring. Great group of supportive people from near and far, with many conditions and advice. Sharing stories of courage, knowledge, and information. They are pillars of hope, cathedrals of inspiration to this hub. So many of them have helped me personally, a great deal, I am truly grateful to all of them. So ask, and the doors shall be opened, seek and you shall find lending helping hands and listening, sending you welcome, peace, blessings, thestorm

[Enya2010 in reply to thestorm]

Thank you it means a lot o know I'm not alone xxx

[Lupiknits]

Hello and welcome! This is a good place to be: I’m very glad I found it.

[Enya2010 in reply to Lupiknits]

Thanks it means a lot to me I'm sure I will get advice and tips from you all xx

[Horsewhisper]

Hi Enya and welcome - you will definitely find what you are looking for here - someone somewhere will help you to find the answers you are looking for and the sharing of your experiences will help others. Xx

[Enya2010 in reply to Horsewhisper]

Thank you it means a lot to know I'm not alone xx

[butterfly1964]

Hi Enya2010,

This forum will be a relief to you and we are all going through different difficulties with our Lupus and related conditions 😩it as been so helpful to me and I am sure it will be for you too..

Welcome jx

[Enya2010 in reply to butterfly1964]

Bless you thank your means a lot to me xx

[Hopes77]

Hello Enya ( love the name by the way ) and welcome x

[Krazykat26]

Hello n welcome Enya 💐

You'll find out about all things autoimmune on here..n we all share our stories!!

Lupus is an illness that makes us feel very alone at times..but this forum is full of people who understand n appreciate how difficult it is living with it 24/7!!

U are not alone 🤗🤗xx

[Enya2010 in reply to Krazykat26]

Thank you it means a lot to me as god it gets me down but thank you for caring xx

[Krazykat26 in reply to Enya2010]

We're all in the same boat so we have an understanding of what u r going through.

Lots of cyber hand holding here 🤝🤝🤝xx

[Paul_Howard Partner LUPUS UK]

Hi Enya2010 ,

Welcome to the LUPUS UK Community Forum. I hope that you'll find this a great place for information, support and to make new friends.

If you're also interested in meeting other people living with lupus in person, we have a network of regional groups across the UK. You can find your nearest one on our website at lupusuk.org.uk/regional-gro...

We also have a team of trained volunteer telephone contacts. If you'd like to speak with someone in this way, please let me know and I can provide you with more details.

If you need more information about lupus and LUPUS UK we have a free pack which you can request or download from our website at lupusuk.org.uk/request-info...

If you need anything else, please let me know and I will do my best to be of assistance.

[Lily77]

Hello Enya, thank you for reaching out and joining the site. There are some very special people on this site offering a wealth of information and invaluable support. I am delighted that you are now also a member. With my very best regards, Lily77

[Enya2010 in reply to Lily77]

Bless you thank you it means alot to me xx

[GlasgowHen]

Hi, welcome and really glad you found your way here. Hope you find it to be a supportive place to be

[Enya2010 in reply to GlasgowHen]

Me too thank you for replying it means a lot

[Han41]

Hi Enya

I'm 42 was diagnosed with SEL last year and now have lupus hepatitis x

[Enya2010]

Oh bless you it sucks xx

[Swimming234_]

Hi , my name is Roberta, I'm 40years old. I'm also looking for a friend with similar condition. I was diagnosed with SLE 5years ago, since diagnosed I have had lots of joint pains and fatigue and lost few friends. it has not been easy and has been a very lonely experience.