Who else has Autonomic Neuropathy?
The Mayo Clinic in Phoenix diagnosed me with Autonomic Neuropathy in 2014. I don't see any reference to that form in any of the information or discussions. I know it effect's my balance, body temperature variance and possibly thinking. Any one have this diagnosis? Seems to be worsening as I age.
Interested in more discussions like this? Go to the Neuropathy Support Group.
@dwlowrance thank you for your input. Cheers to you.
@runnergirl 13 years is a long time. Is autoimmune autonomic neuropathy a more generic diagnosis with less targeted treatments?
You will notice that I moved your question to a previous discussion related to this topic.
You'll notice that members like @avmcbellar @juanito have discussed autoimmune autonomic neuropathy here and may be able to offer information, suggestions, or support.
You may wish to scroll through previous posts and connect with members like @tigreyes2004 @bethunger @kelsey1234 @kenbahler2004 @sunnyflower @ncameron @fiesty76 that are active in the neuropathy group.
- Member Neuropathy Journey Stories: What's Yours? https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/
May I ask what the difference is between Rituxan and CellCept?
@erikas Thanks for responding to my post.
Autonomic neuropathy is not necessarily a generic diagnosis. It's just not as common as other causes as SFN. As for treatments, I'm working with my doctors on trying to find one.
Regarding the drugs, Rituxan targets the B cells and CellCept targets the T cells.
@juanito I'm so sorry to hear of all the challenges you've been dealing with. This disease is certainly emotionally distressing. May I ask where you read about the 5-10 year life expectancy after diagnosis?
Thanks again!
Please I will like to get in touch with you privately to enlighten me more on how to cope with AN, it is a new journey with countless challenges.
Kindly drop yours so that I can write you straight away, please.
Please I will like to get in touch with you privately to enlighten me more on how to cope with AN, it is a new journey with countless challenges. ** Can you send my your contact information in a private message?
Kindly drop yours so that I can write you straight away, please.
@ubikings - We removed your personal email address from your message above. We recommend not posting personal contact information in the public forum. You can use the secure private message function to exchange contact information with @mstephen or another member.
To send a private message, click on the members username and then click the Send private message link at the bottom of their profile description.
I was diagnosed with post Covid POTS about 6 months ago. Is anyone familiar with this? I'm wondering if it is the same as regular POTS or if maybe it will go away with time like some people who have long covid reactions for a year or more
Autonomic Neuropathy is the condition of a loved one. He has diabetes T2. What can he do and what physician specialty should manage his care.
Welcome @jart. Type 2 diabetes is the most common cause of autonomic neuropathy. When poorly controlled, the diabetes increases the risk of autonomic neuropathy and other nerve damage.
Jart, you'll notice that I moved your message to this existing discussion about AN.
- Who else has Autonomic Neuropathy? https://connect.mayoclinic.org/discussion/autonomic-neuroapthy/
I did this so you can connect with other members like @runnergirl @juanito @sunnyflower and many others.
Typically people with AN are in the care of neurology. See more here: https://www.mayoclinic.org/diseases-conditions/autonomic-neuropathy/diagnosis-treatment/drc-20369836
Is your loved one able to control his diabetes? Is he currently in the care of a neurologist?
Neurologist made the diagnosis. No, his BS is not well-controlled and until he becomes convinced he MUST do that, I guess there’s nothing much more that can be done. (He’s on max meds from Endocrinologist.). BUT, he’s got something else too so next is a hematologist. In testing they found protein issues in his blood. Something called MGUS as well as Kappa Lambda Free Chain irregularities. Not a good sign, I know. I imagine a bone marrow test is next. I “think” what they may be looking for is a possible MM diagnosis.