You deserve a big bear hug! Thanks for your response to my journal. You are an awesome mum - I am so impressed with your dedication to your kids. Know I'm out here if you ever need an ear.
Thank you for adding me as a friend :). Hope you are well!
Thank you for the online invite! I would love to share stories of our first year with this disease. Looking forward to learning more about you and how you are doing. It's a lot of ups and downs for me right now. One day I'm fine emotionally, the next I am a complete mess. Hopefully that levels out soon! Happy Friday to you! The weekend has been long coming this week...
Just a quick note to say hi!
I just wrote you another really long note that then didn't post Grr
Just in summary it was saying I forgot to say I saw you are a two week newbie, I'm Feb 28th this yr so new too. Please ask me anything at all! What meds you're considering, what you've discussed with MS Neuro or nurse etc, any questions you might have etc.
this group is fab, sometimes daunting to post on the main site though
I'm just down the road in Stratford upon Avon
Thank you, always nice to make a new friend on the forum. I'm still struggling a bit with the new layout - can never tell who is writing or responding from the main page which is v sad.
I'm doing well myself, Tecfidera all ok with only a few side effects which whilst not nice are manageable. Have to see what scan says next year I guess! I went from 7 active in Feb to none on last scan in about May and some shrinkage of old ones - hadn't even started Tecfidera! I take daily high dose Vit D, magnesium, general multivitamin with added evening primrose, sunflower and cod liver oil (think that's the mix, brain a bit foggy on memory stuff!). I started that in March after my dx and before Tecfidera so have kept going!
Hope you're doing ok too
Glad to have the opportunity. Yet another reason this community is so awesome.