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Yes I had a terrible case Of Bronchitis That I couldn't shake and I walked into a holistic store and this woman gave me a Foot bath - Ionizer with salts and I spoke with this Man for about 2 Hours and I Looked down and there was all this thick Green sludge and awful Looking stuff that came Out of My Lymph system . I saw her a second time and the water was a light yellow - nothing Came out . I was cured immediately after walking Out of that store. Another woman Elizabeth Mintor a scientist at GW told me she cured her dad of alzherimers with a machine form Hulda Clark got all the heavy Metals out of him . I Got a African leash eating mite and she had them too and they would not treat me , she called me and said " I heard they wouldn't treat you at the clinic - I had them too. takes about 3 years to get rid of them . " We Met she wanted My Car to do research but she had a 6 year Old boy and I said " I can't give you my Car . " I couldn't let the Little boy get these damn parasites . I Know what they are too - spoke with the NIH and Gave Blood samples . Luckily The Doctor at Howard University had seen them several times - a tiny Biting Fly from Africa . Howard university saved My Life. I do think perhaps Mushrooms Maybe able to cure Dementia .
Are you diabetic, or is your neuropathy from something else?
What have you tried so far?
My husband has non-diabetic neuropathy in his fingertips. It's not bad yet, but he's had all kinds of tests and therapies and nothing has really helped. He does take Nervive, which helps a little bit, but it affects his stomach.
My walking partner, has diabetic neuropathy, he says there isn't much you can do but walk, makes him a little unsteady at times. So I think moving is probably the best thing. They make these little like bike peddling machines on line, they are not very expensive, to get the blood flowing in your legs.
Moms getting it, I think it's from a degenerative spine.
Sorry you are going through this, I've heard it's very painful and feel much for people with it.
Do some Hot epsom salt baths , soak your feet . See an acupuncturist and swim In the Ocean or Pool . Massage your feet and Legs , drink Lots fo pure water .
My husband has CIDP - Chronic Inflammatory Demyelinating Polyneuropathy, an autoimmune disorder that causes his body to attack the myelin sheath around the nerves. It causes numbness in his feet primarily, with some also in his hands and lower legs.
He sees a neurologist and a podiatrist for this condition.
He has had multiple IVIG treatments to stop the progression of the neuropathy, which so far has worked. It hasn't made him any better, but he hasn't gotten worse, either.
He takes Lyrica for the associated pain, which works well for him. His neurologist also has him on a vitamin B complex, to help with the nerve conductivity.
He sees his podiatrist every 6 weeks. Much like diabetic neuropathy, as he has no feeling in his feet, he has to be wary of ulcerations. The CIDP has given him an additional condition called Charcot foot, which is changing the bone structure of his feet, which can lead to bone spurs and ulcerations. When he has an ulceration, he must wear a crow boot for anywhere from 6-8 weeks, depending on the severity of the ulceration.
He wears "rocker bottom" shoes to help with the balance issue. He also has special orthotics for his shoes, which are routinely measured and changed according to his changing foot structure. These also help with balance issues.
Early on, he was told one of the best ways to help keep the condition at bay, to help him keep his balance and be able to continue to walk, was to keep active. Walking really isn't a great option for him anymore, so he swims every day (3000-5000 yards, depending on the day). Core exercises also help with balance and strength. Movement will keep the stiffness at bay; there really isn't much they can do for the neuropathy, unfortunately.
If you don't regularly see a podiatrist, I would recommend that be your first appointment. They are generally the best versed in foot neuropathy, and I'm sure can give you advice relative to your particular case. Our podiatrist is wonderful, and extremely knowledgeable about all the things that can cause foot neuropathy.
IVIG infusions do help some with neuropathy in my feet.
Penetrex cream on Amazon helped my mother, she'd massage it into her feet and lower legs for relief.
Cymbalta antidepressant was the #1 medication that took my mom's neuropathy from a 10 down to a 2. Speak to your doctor about the pros and cons of this drug.
Sounds like I have a milder version. I have put my feet and ankles in cold water for ten minutes and the elevate for fifteen minutes. I then warm them up with a blanket. Mine is a circulation issue from lose of a toe. Juvenon makes a product that also helps $$, it is a cumulative effect. Good Luck
Something like Circular (peripheral) neuropathy, that adjective is a wrong word, but that's close see a Doctor. Get a second professional opinion And first.Lol. Iafidemia.
Lymphedema has nothing at all to do with neuropathy which is nerve damage. Lymphedema is a condition where the extremities become swollen as a result of damage to the body's lymphatic system, mainly the lymph nodes.
Make sure that you don't have a B12 or folic acid deficiency. I do and if I have forgotten to book my B12 injection, the neuropathy gets worse and my feet and ankles suffer. I can't absorb B12, but if you don't have that issue, do make sure you eat plenty of foods containing it, or take supplements.
I only found out about the B12 anaemia when it had got dangerously low, affecting my memory and capillaries leaking blood into my ankles. I had no idea the two things were connected, but my GP sent me for tests straight away when I mentioned both problems. I had a course of injections every day for a week (or 2 - can't remember!). Now, I have one every 3 months. I'm late again and my right ankle has a black "bruise" and pain from leaking blood vessels.
Interesting to hear, hubs had a diabetic incident which hospitalized him a few days. Bloodwork showed B1 B12 deficiency n GP prescribed 30 day regimen Rx. He’s also alcoholic n dementia. I sure noticed a difference in his mental n physical capabilities within the short period of his release n now two months later since not taking his B’s. I will bring to his doctors attention next visit!
When a started wearing shoes in the house and studio instead of just outside the neuropathy went almost away. Doesn't bother me much now, though I hate wearing shoes in the house.
See your doctor for referrals 1st try a podiatrist, 2nd try a orthopedist, 3rd try a neurologist.
You need to know the source of your stiffness and neuropathy in order to treat it adequately. Get orthopedic inserts in your shoes that any of them recommend.
Peripheral neuropathy is an umbrella term for nerve diseases that affect a specific subdivision of your nervous system. Many different conditions can cause peripheral neuropathy, which means a wide range of symptoms is also possible. Peripheral neuropathy can also affect different body parts, depending on how and why it happens.
What this name means
The term “peripheral” is from the Greek word that means “around.” “Peripheral” in this context means outside of or away from the “central” nervous system. The term neuropathy combines two words that trace their origins back to ancient Greek:
Neuro-: From the Greek word “neuron,” meaning “nerve.” -pathy: From the Greek word “pathos,” meaning “affliction” or “condition.”
Your nervous system has two parts, the central nervous system and the peripheral nervous system.
Your brain and spinal cord are the two components that make up your central nervous system. Your peripheral nervous system consists of all the other nerves in your body. It also includes nerves that travel from your spinal cord and brain to supply your face and the rest of your body.
Peripheral neuropathy can refer to any condition affecting your peripheral nerves. Healthcare providers often use the terms “neuropathy” and “polyneuropathy” (meaning “disease of many nerves”) interchangeably with “peripheral neuropathy.” Peripheral nerves are farthest from the central nervous system, and they often show the earliest and most severe effects of these conditions
Who does peripheral neuropathy affect?
Peripheral neuropathy can affect anyone, regardless of age, sex, race or ethnicity, personal circumstances, medical history, etc. However, some people are at greater risk for specific types of peripheral neuropathy (see below under Causes and Symptoms for more about this).
Peripheral neuropathy is also very common with some age-related diseases. That means the risk of developing peripheral neuropathy increases as you get older.
How common is this condition?
Peripheral neuropathy is common, partly because this term refers to so many conditions. About 2.4% of people globally have a form of peripheral neuropathy. Among people 45 and older, that percentage rises to between 5% and 7%.
How does this condition affect my body?
To understand how peripheral neuropathy affects your body, it helps to know a little about the structure of neurons, a key type of cell that makes up your nerves. Neurons send and relay signals through your nervous system using electrical and chemical signals. Each neuron consists of the following:
Cell body: This is the main part of the cell.
Axon: This is a long, arm-like part that extends outward from the cell body. At the end of the axon are several finger-like extensions where the electrical signal in the neuron becomes a chemical signal. These extensions, known as synapses, lead to nearby nerve cells.
Dendrites: These are small branch-like extensions (their name comes from a Latin word that means “tree-like”) on the cell body. Dendrites are the receiving point for chemical signals from the synapses of other nearby neurons.
Myelin: This is a thin layer composed of fatty chemical compounds. Myelin surrounds the axon of many neurons and acts as a protective covering.
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
That would be my 1st step, after seeing my chiropractor and massage therapist regularly.
What have you tried so far?
My husband has non-diabetic neuropathy in his fingertips. It's not bad yet, but he's had all kinds of tests and therapies and nothing has really helped. He does take Nervive, which helps a little bit, but it affects his stomach.
Moms getting it, I think it's from a degenerative spine.
Sorry you are going through this, I've heard it's very painful and feel much for people with it.
He sees a neurologist and a podiatrist for this condition.
He has had multiple IVIG treatments to stop the progression of the neuropathy, which so far has worked. It hasn't made him any better, but he hasn't gotten worse, either.
He takes Lyrica for the associated pain, which works well for him. His neurologist also has him on a vitamin B complex, to help with the nerve conductivity.
He sees his podiatrist every 6 weeks. Much like diabetic neuropathy, as he has no feeling in his feet, he has to be wary of ulcerations. The CIDP has given him an additional condition called Charcot foot, which is changing the bone structure of his feet, which can lead to bone spurs and ulcerations. When he has an ulceration, he must wear a crow boot for anywhere from 6-8 weeks, depending on the severity of the ulceration.
He wears "rocker bottom" shoes to help with the balance issue. He also has special orthotics for his shoes, which are routinely measured and changed according to his changing foot structure. These also help with balance issues.
Early on, he was told one of the best ways to help keep the condition at bay, to help him keep his balance and be able to continue to walk, was to keep active. Walking really isn't a great option for him anymore, so he swims every day (3000-5000 yards, depending on the day). Core exercises also help with balance and strength. Movement will keep the stiffness at bay; there really isn't much they can do for the neuropathy, unfortunately.
If you don't regularly see a podiatrist, I would recommend that be your first appointment. They are generally the best versed in foot neuropathy, and I'm sure can give you advice relative to your particular case. Our podiatrist is wonderful, and extremely knowledgeable about all the things that can cause foot neuropathy.
Good luck!
Penetrex cream on Amazon helped my mother, she'd massage it into her feet and lower legs for relief.
Cymbalta antidepressant was the #1 medication that took my mom's neuropathy from a 10 down to a 2. Speak to your doctor about the pros and cons of this drug.
Good luck to you.
I have put my feet and ankles in cold water for ten minutes and the elevate for fifteen minutes. I then warm them up with a blanket. Mine is a circulation issue from lose of a toe. Juvenon makes a product that also helps $$, it is a cumulative effect. Good Luck
My issue is circulatory.
And first.Lol. Iafidemia.
I can't absorb B12, but if you don't have that issue, do make sure you eat plenty of foods containing it, or take supplements.
I only found out about the B12 anaemia when it had got dangerously low, affecting my memory and capillaries leaking blood into my ankles. I had no idea the two things were connected, but my GP sent me for tests straight away when I mentioned both problems. I had a course of injections every day for a week (or 2 - can't remember!). Now, I have one every 3 months. I'm late again and my right ankle has a black "bruise" and pain from leaking blood vessels.
1st try a podiatrist,
2nd try a orthopedist,
3rd try a neurologist.
You need to know the source of your stiffness and neuropathy in order to treat it adequately. Get orthopedic inserts in your shoes that any of them recommend.
https://my.clevelandclinic.org/health/diseases/14737-peripheral-neuropathy
In part, it says: What is peripheral neuropathy?
Peripheral neuropathy is an umbrella term for nerve diseases that affect a specific subdivision of your nervous system. Many different conditions can cause peripheral neuropathy, which means a wide range of symptoms is also possible. Peripheral neuropathy can also affect different body parts, depending on how and why it happens.
What this name means
The term “peripheral” is from the Greek word that means “around.” “Peripheral” in this context means outside of or away from the “central” nervous system.
The term neuropathy combines two words that trace their origins back to ancient Greek:
Neuro-: From the Greek word “neuron,” meaning “nerve.” -pathy: From the Greek word “pathos,” meaning “affliction” or “condition.”
Your nervous system has two parts, the central nervous system and the peripheral nervous system.
Your brain and spinal cord are the two components that make up your central nervous system. Your peripheral nervous system consists of all the other nerves in your body. It also includes nerves that travel from your spinal cord and brain to supply your face and the rest of your body.
Peripheral neuropathy can refer to any condition affecting your peripheral nerves. Healthcare providers often use the terms “neuropathy” and “polyneuropathy” (meaning “disease of many nerves”) interchangeably with “peripheral neuropathy.” Peripheral nerves are farthest from the central nervous system, and they often show the earliest and most severe effects of these conditions
Who does peripheral neuropathy affect?
Peripheral neuropathy can affect anyone, regardless of age, sex, race or ethnicity, personal circumstances, medical history, etc. However, some people are at greater risk for specific types of peripheral neuropathy (see below under Causes and Symptoms for more about this).
Peripheral neuropathy is also very common with some age-related diseases. That means the risk of developing peripheral neuropathy increases as you get older.
How common is this condition?
Peripheral neuropathy is common, partly because this term refers to so many conditions. About 2.4% of people globally have a form of peripheral neuropathy. Among people 45 and older, that percentage rises to between 5% and 7%.
How does this condition affect my body?
To understand how peripheral neuropathy affects your body, it helps to know a little about the structure of neurons, a key type of cell that makes up your nerves. Neurons send and relay signals through your nervous system using electrical and chemical signals. Each neuron consists of the following:
Cell body: This is the main part of the cell.
Axon: This is a long, arm-like part that extends outward from the cell body. At the end of the axon are several finger-like extensions where the electrical signal in the neuron becomes a chemical signal. These extensions, known as synapses, lead to nearby nerve cells.
Dendrites: These are small branch-like extensions (their name comes from a Latin word that means “tree-like”) on the cell body. Dendrites are the receiving point for chemical signals from the synapses of other nearby neurons.
Myelin: This is a thin layer composed of fatty chemical compounds. Myelin surrounds the axon of many neurons and acts as a protective covering.
Lots more information available.
Gena / Touch Matters