[erjlg3]

Just a quick hello. So glad to have found this site. Finally have found one doctor who has barely touched on finally telling me I am having neuropathy symptoms............after telling so many doctors my symptoms and getting no feedback whatsoever and all doctors except this Neurologist.....ignoring me telling them the symptoms I am having. After reading some of the post..........I know this is what I have.........adding to all of the other things. It's scary and I am going to believe that I can get somewhat better.......I just need to find out how. Thanks all for this site. It looks like I have so much more reading to do some time.
Jackie

[Darlene]

Jackie,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Sad to hear you your situation, click onto the following forum, there are dear friends there to help you out.

Peripheral Neuropathy:
http://neurotalk.psychcentral.com/forum20.html

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

[erjlg3]

Thank you so very much Darlene. It helps to know people are there when you are scared and there to help you through. hug:

[Brain patch]

Hi Jackie,
Welcome. This is a great site, I have found so much support here and some really good friends as well. I am sorry you are suffering. I know the other people on here that suffer with this same thing will be able to give you a lot of help and support. Just knowing you are not alone helps. Speaking to others that understand and are going through the same thing is so relieving. I wish you the best of luck in your recovery.
Brain

[pete81241]

and i hope we can support each other as we get to know the ropes....pete

[erjlg3]

Originally Posted by Brain patch

Hi Jackie,
Welcome. This is a great site, I have found so much support here and some really good friends as well. I am sorry you are suffering. I know the other people on here that suffer with this same thing will be able to give you a lot of help and support. Just knowing you are not alone helps. Speaking to others that understand and are going through the same thing is so relieving. I wish you the best of luck in your recovery.
Brain

Thank you and I do feel better knowing all of you are here and hoping I will find out how to feel better. I am sorry that we all hurt

[erjlg3]

Originally Posted by pete81241

and i hope we can support each other as we get to know the ropes....pete

Yes. We have a lot of ropes to learn It's overwhelming lately. Everything seems like a mountain when you are in pain.

[cindylou_38]

Hope you find answers here, welcome

[Toni-lynne]

Originally Posted by erjlg3

Just a quick hello. So glad to have found this site. Finally have found one doctor who has barely touched on finally telling me I am having neuropathy symptoms............after telling so many doctors my symptoms and getting no feedback whatsoever and all doctors except this Neurologist.....ignoring me telling them the symptoms I am having. After reading some of the post..........I know this is what I have.........adding to all of the other things. It's scary and I am going to believe that I can get somewhat better.......I just need to find out how. Thanks all for this site. It looks like I have so much more reading to do some time.
Jackie

Hi Jackie welcome to Neuro talk and yes you have found the right place the people here are very helpfull. I really enjoy the chat rooms where I have talked to many people with some of the same issues as myself and also very understanding. I have neuropathy also and can tell you it is the worst pain I have ever had and hard to describe, it has been a rough road but finally am seeing a pain management specialist and he has had me go through 8 weeks of physiotherapy now on a pain treatment with medication. The way I feel now is so much better than before its like I have some of my life back. It takes a lot and has been a real journey that I am still on. If I can be of any help with information I have please just ask

Toni