# Neurologist this morning **URL:** \ **Category:** General\ **Created:** [July 8, 2013, 12:45pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663 "2013-07-08T12:45:51Z")\ **Posts on this page:** 9\ **Page:** 1
**Author:** ![Jackie51](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/jackie51/32/1208_2.png) [@Jackie51](https://forum.livingwithfibro.org/u/Jackie51)\ **Post date:** [July 8, 2013, 12:45pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/1 "2013-07-08T12:45:51Z")
This morning at 10:15 I will see my neurologist about the brain MRA, from last week. I certainly hope that the lesions on my brain that they found 3 months ago, and have been watching with MRI each month will not have grown anymore from last month! I also hope that he finally decides what it is he is diagnosing from the MRI's! Scared, but need answers! I just pray for a positive outcome@ Tired of the hand tremors, they are so noticible.. ---
**Author:** ![mrsg](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/mrsg/32/1863_2.png) [@mrsg](https://forum.livingwithfibro.org/u/mrsg)\ **Post date:** [July 8, 2013, 1:59pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/2 "2013-07-08T13:59:35Z")
Good luck and prayers sent your way 🙂 ---
**Author:** ![Jackie\_S](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/jackie_s/32/1503_2.png) [@Jackie\_S](https://forum.livingwithfibro.org/u/Jackie_S)\ **Post date:** [July 8, 2013, 3:24pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/3 "2013-07-08T15:24:37Z")
Jackie, Please let us know what the Dr. says today. You are in my thoughts and prayers. Jackie S. ---
**Author:** ![Jackie51](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/jackie51/32/1208_2.png) [@Jackie51](https://forum.livingwithfibro.org/u/Jackie51)\ **Post date:** [July 8, 2013, 3:41pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/4 "2013-07-08T15:41:15Z")
MS is the diagnosis. Records being transferred to Hershey medical for treaent plan ---
**Author:** ![Jackie51](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/jackie51/32/1208_2.png) [@Jackie51](https://forum.livingwithfibro.org/u/Jackie51)\ **Post date:** [July 8, 2013, 4:23pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/5 "2013-07-08T16:23:39Z")
Tammy, I just got home from this appt. my mail came, and I was denied ssdi! What do I do now? I shake so badly I can't keep things in my hands. I just want to cry, this is so unreal! ---
**Author:** ![purplebutterfly](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/purplebutterfly/32/1839_2.png) [@purplebutterfly](https://forum.livingwithfibro.org/u/purplebutterfly)\ **Post date:** [July 8, 2013, 4:33pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/6 "2013-07-08T16:33:41Z")
With the new diagnoses I would talk to social security and either reapply or appeal this decision. I will be thinking of you. When do you go to the other doctor? ---
**Author:** ![Jackie51](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/jackie51/32/1208_2.png) [@Jackie51](https://forum.livingwithfibro.org/u/Jackie51)\ **Post date:** [July 8, 2013, 4:36pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/7 "2013-07-08T16:36:36Z")
My dr said it takes Hershey medical 3 weeks to get me on a treatment pla n ---
**Author:** ![Rachel\_Pronyshyn](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/rachel_pronyshyn/32/104_2.png) [@Rachel\_Pronyshyn](https://forum.livingwithfibro.org/u/Rachel_Pronyshyn)\ **Post date:** [July 8, 2013, 8:23pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/8 "2013-07-08T20:23:49Z")
Oh Dear Jackie I am just reading this Discussions now. I am so sorry that you have now been diagnosed with MS to add to your diagnosis of Fibromyalgia. I'm sure it just doesn't seem fair. And then you come home from the doctor's appointment to find the letter of denial for disability. However some members here can and are giving you some advice which sounds good. Now with this new diagnosis perhaps you will be more successful in refilling. I pray that you are successful. Gentle hugs Rachel ---
**Author:** ![Jackie\_S](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithfibro.org/jackie_s/32/1503_2.png) [@Jackie\_S](https://forum.livingwithfibro.org/u/Jackie_S)\ **Post date:** [July 9, 2013, 4:36pm UTC](https://forum.livingwithfibro.org/t/neurologist-this-morning/2663/9 "2013-07-09T16:36:02Z")
Jackie, I am so sorry about your MS diagnosis. And so sorry you were denied SSD. I do think you are getting some good advice from the ladies here about how to go about keeping the wheels moving on your SSD claim. Know we are all here for you and please keep us informed on how things are going for you. You are in my thoughts and prayers! Jackie S.