I have found a lot of support through MSpals. I have met some wonderful people and I have been able to get some terrific advice. My work on the website allows me to pay my positives forward while giving me an additional thing to feel positive about!
MSpals wants YOU!
This is all to say that MSpals wants you! I would love to share your story here. Whether you have something specific to say about how MSpals impacts your life, or you just want to share you special talent. MSpals is about building connections and showcasing our members, who are strong and fabulous even with MS!
We don’t expect you to make MSpals a job, especially when you may barely have enough energy for most days! We want to empower you to make MSpals what you need! Maybe you need to publicly proclaim your gratitude to someone for listening when you needed to vent. Maybe you want to introduce yourself to make it easier to make new friends. Maybe you have a neat way for dealing with the super-hot days of summer, and you thin all MSers should know about it! While we do not endorse any specific treatment plan, we would love to hear about things that make your life better!
Share and share alike!
Most importantly, MSpals would like to give you an outlet. We want to make sure that you know your voice is heard! If you post something in one of the FaceBook groups and would like to get a bigger response, we want to know about it! MSpals is about the pals! Please reach out to us here and be a pal!
If you have a suggestion about something that might make MSpals work better for you, let us know
True those. I’d like to read comments from other Pals when they like (or don’t like) something I’ve posted in “Pins and Tips”. Did you try it did it work for you? Did you modify it and like it better?
I cant help but comment on all of u wanting to help those w/MS issues. What i would like to see is a list of drs who diagnosis MS, their contact info. Mary Pettitgrew who is your fab dr who took the time to explain your diagnosis? There r still plenty of us still searching (45yrs) for that diagnosis. A lot of us with symptoms have just realized we have MS & need these drs info who know how to diagnosis but a lot of us dont have tge same opportunity to find any dr that can Diagnosis. I read too many times to ask ppl already Dx with MS who they ho to. That doesnt work for many us of living in states who may have 1-2 drs that specialize n MS. & have been dismissed because we r too old. I would b willing to travel to see an experienced dr than keep going the way ive been live which is “we just dont know whats wrong with u”!