So proud of this group.

[Oxford8]

I felt so immensely proud of this group when I checked in just now. Yhere was a desperate request for information from lola5670. In no time at all appeared wonderful helpful and warm responses from our ambassadors and volunteers.

Mrs. Nails, Dorset Lady, PMRpro and all you other responders Thank you. 👏👏👏👏👏.

I could almost feel the relief of lola5570 as she received such sensible advice.

Very proud! 👍👍👍🌷

[Suet3942]

It’s a wonderful site. Thank you to everyone.

[SheffieldJane]

I feel like that often. Particularly when PMRPro takes on something seemingly insolvable and makes it manageable. We are very lucky.

[Marlenec in reply to SheffieldJane]

Yes Jane we certainly are, and I know I don't thank everyone enough! Well said Oxford8.

[Hidden]

Thank You Oxford8 💐

[PMRpro Ambassador]

Thank you!

[EdithWales]

Thank you Oxford

[YuliK]

Wonderful group of ladies. Thank you for all your help and advices. First class all of you. ❤️

[bunnymom]

Thanks to all of you who pitch in on a regular basis... official or unofficial. I read everything everyday. This site is a great source of info and comfort as we navigate the new normal. ☀️

[DorsetLady PMRGCAuk volunteer]

🌷

[Pollypuds]

I value the information and contact with others who actually know how difficult this ailment of ours can be to live the immensely.

[Lanakay]

I read this instead of a morning paper while I have my coffee. Then no matter who in my life doesn’t understand what living with PMR is like I know my friends here do.

[Lonsdalelass]

Yes, it's wonderful! A big thank you to everyone for all your continued help and advice.

[Jackoh]

Yes I think we would all very lost without this site!

[Hidden in reply to Jackoh]

Too True Jackie!

[Ozark]

An excellent observation Oxford8. I have posted a number of questions to this group and have always received quick and thoughtful replies. For someone like myself who lives alone and who has no outside support that "really" understands this disease this group invaluable. I normally don't offer advice as I feel there are others on this site better qualified than myself to do so. Though I suppose as a fellow sufferer I guess I'm somewhat qualified to offer a word or two now and again. This community is an invaluable resource to all of us with this relatively rare disease. My hat is off (to use an old expression) and my heart goes out to everyone in this group.

[PMRpro Ambassador in reply to Ozark]

EVERYONE can have something of value to contribute providing it is relevant to living with PMR or GCA.

[Hidden in reply to Ozark]

I concur with PMRPro

[Joaclp]

Hear, hear.🌹🌹🌻🌻