← Return to Demylinating Sensorimotor Neuropathy vs./ or and Polyradiculopathy
DiscussionDemylinating Sensorimotor Neuropathy vs./ or and Polyradiculopathy
Autoimmune Diseases | Last Active: Mar 5 10:29am | Replies (29)Comment receiving replies
Replies to "I am on a similar journey for answers. My journey started in 2011 (in my early..."
Hello Daily Hope,
I like your name 😊
I don’t know where to begin. When I first read your post, I was speechless. Complicated doesn’t begin to cover the extensive issues you have faced - are facing.
You mentioned an orthopedic doctor. Is he/she who diagnosed you with your spinal issues? I ask because at first my rheumatologist ordered mri then neurologist.
I have newer symptoms. I see the neurologist soon. I hope she follows with neck and thoracic imaging. I’ve got newer issues with worsening expanded symptoms. I am not sure if it is her department, I will find out. I need answers so I can get the right treatment. Quite frankly, I feel like I’m diseased. The body is fighting battles…that its not winning. I’m sorry I didn’t respond right away. Honestly, I was overwhelmed.
I hope doctors are helping you with your conditions. This is a wonderful place for support.
Hope is so important to have when so much is going on.
I pray you receive the help you seek and real answers, therapies to assist you.
I have to say, you sound so strong, like a fighter and that is so good! That is half the battle!
One word keeps coming to my mind ‘outreach’.
Please let us know how things progress.
Take Care
🩷
We are all here because we have complicated issus and your's is certainly up there. I wish some of us could be there for you to just make a cup of coffee when you need it. But we are there in spirit and wish you more than the best.
♥️