Hello everyone. Not sure what ... - Fibromyalgia Acti...

Fibromyalgia Action UK

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Hello everyone. Not sure what ...

MorganRaven profile image
7 Replies

Hello everyone.

Not sure what to write. So much is wrong and seems to be getting worse

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MorganRaven profile image
MorganRaven
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7 Replies

Sorry to hear this, maybe write about one problem at a time and maybe some of the lovely peeps here could come up with some helpful suggestions ?

take care

Jacqueline x

Janet28 profile image
Janet28

Hi MorganRaven welcome to our wonderful forum ☺ I'm sure you will come to find the forum invaluable in chatting to others who are going through the same experience as you, talking to others at different stages of their lives with Fibro and learning from their experiences.

It does help with the whole process and I wish I had found the site years ago. I have had Fibro for nearly 30 yrs and I'm still learning about it, like we all are.

What the best thing to do my friend is read through posts and see how the forum works. If you look to right of screen under Pinned Posts you will see a number of links that will help you to navigate the forum.

Please do go look at the mother site where you will find all the information you need and lots of useful links on Fibro and I look forward to chatting to you on the forum.

fmauk.org

Peace, luv n light

Jan ☺

PS. I advise you to lock your post to keep info safe from internet. Pls. follow this link to simple instructions .You will get more replies on a locked post too.

healthunlocked.com/fibromya...

BlueMermaid3 profile image
BlueMermaid3

Hello MorganRaven

Welcome to the forum :)

As you say you don't know where to start with everything that is going wrong, why don't you start by letting us know some things about you.

For example, how long have you had Fibromyalgia? Do you have any other conditions to contend with as well?

I was just wondering whether you have used your own name as your username?

If you have, I would strongly recommend that you change it to something that cannot identify you.

If you would like to know how to change your username:

Click on your username on the top left of your screen

Click on "account settings"

Scroll about half way down that page.

You'll then see where to change your name.

Don't forget to scroll to the bottom of the page and click on

Save changes.

If you need any further help, please don't hesitate to give me a shout.

As our Jan has said, it really is a good idea to lock your posts for the sake of internet safety.

If you would like me to lock it for you, please let me know and I'll be happy to do it for you.

Wishing you much peace

Lu x

Administrator

Hartleyhare2 profile image
Hartleyhare2

Hi,

I empathise where your at, many of us will, were all in the same boat just at different stages. There is so much knowledge, support and love here that you just have to open up a bit and it will come flowing to you.

Personally I would get it all out on paper, just let it pour out and probably expect a few tears, don't let them on the ink!

Then you have a good starting point to start asking questions on here and people can reply to a specific issue.

I wish you alll the best but tough love makes me say only you can manage this and seek appropriate help through action.

I hope to see lots more posts from you. Remember asking questions helps those replying as well as you so never restrain from posting.

Bright Blessings of health and hapiness

Patrick x

MorganRaven profile image
MorganRaven

Wow thank you all for the kind words. No it is not my real name lol. Well have had fibro since adolescence. My discs have been bad since I was pregnant with my first child. Have 6 now lol. Each a new challange on my body. Was misdiagnosed with sciatica and bad sarcralotic joint (not spelt right) both wrong. So far have had pills thrown at my was diagnosed with fibro in dec 15 after an op. Have since had one cortisone injection to block the nerve in the l4 nerve and one in my l4 spinal column. Not done much but cause more pain. And I have a numb dead leg. The Raynaurds is another pain as cant leave the house most days living in the uk is no good lol but then Id blister in a hot climate lmao polymorphic light erruption. Gosh my spine seems to be getting worse as more discs are slipping. Im falling apart and finding it hard to stay positive for my family now i feel like a burden to them xx

MorganRaven profile image
MorganRaven

Lol thank you its a blessing.... my eldest is almost 13 lol that comes with problems of its own pre teen rebellion. The others are no help. Hubby is great tho so counters it... i try to live each day as it comes but they are merging together now lol xx

TheAuthor profile image
TheAuthor

Hi MorganRaven

I sincerely hope that you are feeling as well as you possibly can be today? Welcome to the forum and it is wonderful to make your acquaintance.

I want to sincerely wish you all the best of luck and please take care of yourself my friend.

All my hopes and dreams for you

Ken

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