Living with Neuropathy - Welcome to the group
Welcome to the Neuropathy group.
This is a welcoming, safe place where you can meet other people who are dealing with neuropathy. Let’s learn from each other and share stories about living well with neuropathy, coping with the challenges and offering tips.
I’m Colleen, and I’m the moderator of this group, and Community Director of Connect. Chances are you’ll to be greeted by volunteer patient Mentor John (@johnbishop) and fellow members when you post to this group. Learn more about Moderators and Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let’s chat. Why not start by introducing yourself? What concerns would you like to talk about?
Interested in more discussions like this? Go to the Neuropathy Support Group.
I sure will. I don't see the rheumatologist until Aug.6. I think you also asked me to update you on the results of the CAT scan I had done to check my lymph nodes as I was told I had lymphedema but had not had cancer. Well the CAT scan did not show involvement of the lymph nodes so it is edema, but lymph nodes are no blocking the fluid. Now to find out what is. They are now considering a nerve in the spine. Lots of osteoarthritis there.
Hi @summertime4, perhaps a home care agency in your area can help with your lymphedema. I know that some home care therapists are certified on lymphedema. The agency needs an order from your rheumatologist for home care therapy to admit you to their services, The therapist will work with your doctor for orders. They can also help you get fitted for the right sleeve to remove the fluid. You should give it a try and remember it is the patient’s choice with which agency to sign up for services not the doctor. The doctor can assist you but it’s your right to choose. Of course, it all depends on your medical insurance plan but take advantage if you have Medicare as a primary insurance it is at no cost to you for the service.
Are you referring to Physical & Occupational therapists like I was referring to? Those are the types of therapists I’ve gone to. Physical therapy was helpful & I went on to do more (than what they did) by exercising on my own at the Y. The Occupational therapists have been the most disappointing. As I stated, they only know how to help people recovering from, for example, an injury or surgery (injured bones). They’re not trained in providing help for chronic neuromuscular conditions.
Thank you for this information. I did not know this. Someone was to come out and fit me with a sleeve for my leg. Didn't happen and now I just want them to figure out what is going on.
@artscaping I don't know how I missed this information from you but completely agree with you about our healthcare in the USA it leave a lot to be desired that is why Integrative medicine is on the uprise in my opinion. I use the cdb balm I found one at Sprouts its just a cream ,little tube but works for me. There are balms on different sites but for me I get headaches from THC so just stick with Hemp cannabis. We are all different . Liked your post Have a good day
Finding out what is going on will determine the treatment. Hopefully you will find out more through your rheumatologist. You can ask any doctor you see to provide an order for home care for you. Since that doctor will be the one giving the orders and consulting with all the disciplines(i.e. nurses, physical and/or occupational therapists) it makes sense for the doctor to know what is going on in order to be in charge of the home care you receive. If you need any assistance in guidance let me know. For years I worked in that industry.
Sorry to hear about your disappointment but it does depend on where you go for therapy. Each therapist has different training, depending on their interests. You have to find a therapist that specializes in what you need. I met a lot of therapists, occupational, physical, and speech. You need to ask questions to find the right one. I went weekly to an outpatient facility to receive physical therapy. I learned the exercises and then did them on my own at home for better balance. I will use home care next time for physical therapy to learn to walk on an uneven surface like the lawn. With Medicare being the primary medical insurance, the physical therapy services will be at no cost.
I’ve been to numerous physical & Occupational therapists, on & off since 2005. As I stated, the physical therapists did help. They can only go so far & then I went further on my own, going to the YMCA. The Occupational therapists were the big disappointment. My dermatologist told me it needs to be a hand specialist, not just a hand therapist. There’s a big difference he told me.
I recently wanted to start both therapies again. I “interviewed” numerous companies that took my insurance. I even started with a company near my home (even though to my surprise & disappointment they didn’t even have an elliptical). I could tell after day 1 of Occupational therapy the man wasn’t going to know how to do anything different than what previous Occupational therapists have done. I also asked several of my doctors if they could help me find a hand specialist & physical therapist who knows how to work with chronic neuromuscular conditions. No one could help.
I believe if I lived near a bigger specialty clinic like Duke or Mayo it would be easier to find appropriate & qualified therapists.
I am glad to help @summertime4. Once you find out what is going on, call home care agencies to find out what services they offer and specialize in. Ask if any therapists are certified in lymphedema. They may have a physical therapist or occupational therapist that can help you. The certification gives therapists the required training to remove the fluid without causing any other harm. Pushing the fluid too quickly to other areas of the body may cause CHF so make sure the therapist knows what he or she is doing. Once a therapist comes out to your home, he or she may recommend a place for you to go for the proper fitting and purchase of the sleeve. The therapist needs to work with you to get a sleeve. With the right sleeve, they will be able to do more therapy. Depending on the location, the sleeve can be expensive. You may also want to call around places that will provide a sleeve and find out the cost. Hopefully your medical insurance can help cover the cost. Try medical supplies companies in your area. Better to find out ahead of time so you can make better decisions with the therapist regarding your treatment. Plus the therapist will be happy to see you are involved in getting help for yourself. That means a lot.
Anyone have luck with accupuncture for PN?