Not getting email notifications

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DivineMrsM
DivineMrsM Member Posts: 9,620
edited June 2014 in Comments, Suggestions, Feature Requests

All of a sudden, the email notifications I was receiving stopped.  Not sure why, as I didn't change anything on the board. How can this be fixed?

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  • Medigal
    Medigal Member Posts: 1,412
    edited March 2011

    Why would anyone get email notifications just because a new post appears.  I did not know we had this capability and never got any for any of the threads I am on.  Where does one activate this if it is still available.  Thanks!

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  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited March 2011

    At the top of every thread, there is a little blue link to the right that says "Add to My Favorite Topics".  There are some topics I like to keep up with like the Feb and March chemo pals.  So I click on them.  then i went into the "My Favorite Topics" tab.  It has all the topics you have added to your list.  You can then click a link on any or all of them to receive email notifications. It makes it so much easier to keep up with the gals you're going thru the same stuff with.  

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  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited March 2011

    I should say, the email notifications are whenever anyone posts a new reply.  

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  • prayrv
    prayrv Member Posts: 941
    edited March 2011

    My notifications stopped as well - driving me nuts!

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  • nowheregirl
    nowheregirl Member Posts: 894
    edited March 2011

                

    Looks like notifications for new PM's has stopped as well.

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  • Shineygirl
    Shineygirl Member Posts: 1
    edited April 2011

    Hi Timtam,

    I have only just found this site.  I am struggling with TE on my radiated side following a bi-lateral mastectomy in October 2010.  I had previously (Oct. 2009) had two lumpectomies followed by 7 weeks of radiotherapy on the right side only.   My surgeon will not continue with the TE on the right, which I am secretly relieved about as it was very painful.  My scar on this side actually opened a little and I had to have some fluid drained to relieve pressure.  On the 11th April I have a meeting with my surgeon and also some of her collegues to discuss my options.  I appreciate that I have only just joined this site but I would be extremely grateful if I could have access to the pictures of reconstruction posted by others.  I am a competitive tennis player, very active and am extremely worried thatthe use of the lat dorsi muscle, (whichis my surgeons preference) is going to have a big impact on my lifestyle.  I am in a real dilema....on the one hand being active is everything to me, it keeps me mentally healthy as well as physically, on the other hand I would like to have succesful recon.  Any sharing of experiences would be really helpfull.

    Many thanks, Bethan X

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  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited April 2011

    Shineygirl, I don't know if this is the right topic for you to request to see the photos, please search the website so you can find what you're looking for........hope you find other things on the site to help you thru your journey.........

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  • Moderators
    Moderators Member Posts: 25,912
    edited April 2011

    Okay, we're all over this one! So sorry. Not sure what happened. 

    Melissa

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  • buccaneersdj
    buccaneersdj Member Posts: 241
    edited April 2011

    My email notifications have not been working for quite awhile now. I have tried removing them and then adding it again, but it still doesn't work! ArGGG!

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