Forum Discussion

MamabearPam's avatar
12 years ago

New Player- Introducing myself

Now that's how you do a first/introductory topic!

Hi Pam! *waves* ^_^
  • Welcome, Pam!

    I have PTSD, and acute, chronic pain, in what little I can feel of my legs from the knees down. I'm actually finding the med topic here pretty interesting. In any case, I frequent these forums regularly lately, so feel free to add me if you'd like. My town is a bit crashy at the moment due to its size, but I plan on downsizing it in the near future. Nice "win" with the invite thread, btw; most get b*tch-slapped away pretty quickly, haha. 32, F, FL, USA.
  • Hi Pam,
    I had trouble adding you and accepting your request. I'm not sure what happened since that account only has the other Springfield and "me" as neighbors. The servers are undergoing maintenance now or shortly, so as I said in my pm to you, I'll try from both accounts tomorrow.

    Any time you have to visit on the forum will be great. My best friend has had one spinal tap, and one was more than enough for her, so I truly sympathize with you on getting several a year. . .
  • Thanks everyone! I will say so far the people here are pretty great! Always pleased to meet new friends.

    Elsie-- I tried adding you, with no luck. I counted, and I'm not at 100 friends. Close, but not there quite yet. I keep getting that "Oops" message popping up REPEATEDLY in that whole section, even when I'm just looking at the updates, so I'm assuming there's an issue. I know I'm getting pretty frustrated, pretty quickly. Emailing EA first thing tomorrow. And if you PM'd me, not sure what happened. I have no messages. AAAHHHH! Frustrated!!! :(

    Again, thank you to everyone for such a wonderful & warm welcome!!
  • fragrlr0ck wrote:
    I’m glad to see space like this pop up in a game specific forum. I started playing this game as stress release from grant writing. My research looks at health care access (in the US) for people living with chronic pain conditions and autoimmune syndromes, or what we refer to in my discipline as “contested” illnesses. Contested illness simply refers to illnesses that are challenging to identify and treat because each person experiences symptoms differently, symptoms range in severity and frequency, and there are oftentimes vague boundaries for diagnosis. Lupus, celiac, PTSD, fibromyalgia, CFS, phantom limb, MCS, and so many others fall under this category. Although each state (or health insurance company) has a different set of guidelines, navigating those guidelines is what I do professionally. If I can ever be of help to anyone please let me know. I may not be able to answer specific questions, but I may have a colleague who can or know of a resource that could be useful.

    Cheers and happy tapping


    Thank you. I myself am from Canada, but I'm sure several here could use assistance. I myself fought with our government disability for eight years before finally getting it. (I think it might even be a record, as I've never heard of anyone waiting that long) I worked & contributed all my life, & then when you need it, they refuse to give it to you. Most of what I suffer from are what you call "contested" illnesses...the Fibro, CFS, Etc. Even my other health problems/illnesses that can be proven, like my Degenerative Disk disease, Arthritis, etc., and the depression & PTSD (which I have too) were turned down. I had literally hundreds of doctor's reports & tests, from my family doctor, multiple specialists, hospitals & pain clinics, yet I was told I could work. It wasn't until I was diagnosed with IH (which is a very rare illness) that they finally granted me my disability. When I finally received it, they stated that I should have been approved upon my initial application & apologized. They also retro payed me 7 1/2 years. Take this as a lesson to NEVER give up! No matter what they say, keep fighting. All this, by the way, WITHOUT a lawyer!
    Thank you for posting about this. It may be the difference in someone's life they need. And you may be the key to helping someone. It's such a difficult road for those of us who suffer with these invisable illnesses & chronic pain.

    Keep the faith & never give up!!