Help please! No diagnosis yet, but believe I have firbromyalgia

[Kelly Anne]

Hey BlueBells. I am in Australia too, Melbourne. Where abouts are you?
I am sure your not a fake and your right the support here is 'phenomenal'.

 

[BlueBells]

Hi @Kelly Anne

I'm halfway between Melbourne and Adelaide. There are a few Aussies on here, no idea how many though.

I think when I replied earlier I got two of you mixed up. I've been a bit foggy, might be worse than I thought. I've been having a good day, but still got only one thing on my list of nine done!

 

[KaseyF63]

@JayCS,
Wow! Thank you for all of this information! I had no idea about Dr. Wolfe! How amazing. I will absolutely look into the KU med/wichita division.

Thank you for the other info as well. This is always so incredibly helpful, as I am so new into this and beyond excited to learn what I can do to take control and having less pain and more energy.

 

[JayCS]

I had no idea about Dr. Wolfe! How amazing

Here are the further branches of that rabbit hole/warren I went down yesterday,
just in case you didn't see, cos they're on the 'research' subforum.

(At the moment I'm calling these rabbit holes "hamster wheels" on my blog,
and my challenge is to simply "jump out" in one leap, which I finally managed to,
but felt good and satisfied with myself for having been in as well as for coming out.)

 

[PANOWLCHAP]

FIND A FM DR FIRST, THEN IF YOU STILL HAVE PROBLEMS WITH RA DR LOOK FOR NEW ONE. THERE ARE A GROWING NUMBER OF DRS IN FAMLY PRATICE THAT BELIEVE IN FM AND TREAT IT. SORRY YOU ARE GOING THRU ALL OF THIS, KNOW YOU ARE NOT ALONE.