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#1 | ||
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Member
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I have only had this hideous disease 4 months and it keeps spreading. Is this common? it's now in my shoulders, upper & lower back and today feels like it's going into my triceps. I thought in most cases it stops at hands, feet, legs. I guess unless a cause is found there's no stopping it. I suppose even the doctors can't answer that question. Frustrated beyond belief! Preforming the smallest chore is huge now.
Cliffman ![]() |
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"Thanks for this!" says: | DejaVu (11-09-2015), St George 2013 (11-09-2015) |
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#2 | |||
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Senior Member
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Hi Cliffman,
I am sorry to hear your symptoms are spreading. It seems odd to me too that SFN would be acting this way so quickly. I had mentioned CRPS when you came on board and I saw that Jo*Mar did as well. Since CRPS does sometimes arise after heart attack it makes me wonder about this possibility. I am attaching an interpretive article from RSD Hope's site about Dr. Louise Oaklander's findings on small fiber damage in CRPS 1. I had found the actual research article some time ago but can't locate it right now. http://www.rsdhope.org/study-confirm...ps-type-i.html This might be something to consider with your doctors. ![]()
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Littlepaw Shine Your Bright Light |
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"Thanks for this!" says: | DejaVu (11-09-2015), Patrick Winter (11-09-2015), St George 2013 (11-09-2015), vintagewine (11-10-2015), zkrp01 (11-09-2015) |
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#3 | ||
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Junior Member
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So sorry for your suffering. I have had this over 15 years now and I remember from the beginning my neurologist at the Mayo Clinic telling me two things. It is still in my hands and feet - BUT, it is like if you stubbed your toe - pretty soon your foot hurts and then your leg. Nerves talk to each other. The other thing he said was there will be a time that your brain will adjust and things that are so hard for you right now will become the norm and there will be an adjustment to living in pain. I remember clearly thinking he was crazy - but truly that was my story. I do live in chronic pain and I do feel it everywhere. (getting my hair done is the worse) HOWEVER you need to find a good neurologist that will help you keep a quality of life - there are good meds that help. Lyrica changed my life and even allowed me to work part time again --- joined with a strong pain killer -- I have continued on with my life. I truly feel for you, but find yourself a doctor that can help. Good luck and keep coming back these people are the best in helping even if you just need to vent! HUGS
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#4 | ||
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Member
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Quote:
__________________
Diagnosis: Idiopathic Small Fiber Neuropathy (Statin Induced) • R-Lipoic Acid: 100mg - 300mg Daily • Acetyl-L Carnitine: 1500mg Daily • Vitamin B12: 1000 mcg Daily • Magnesium 500mg Daily • Grape Seed Extract 200mg Daily • Benfotiamine 300mg daily |
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"Thanks for this!" says: |
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#5 | |||
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Wisest Elder Ever
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I have to wonder if you were given antibiotics when the stents were placed? Fluoroquinolones, cause PN in some people.
(Cipro, Levaquin, Avelox, Flagyl, Tindamax)
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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"Thanks for this!" says: |
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#6 | ||
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Member
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Quote:
Thanks, Cliffman ![]() |
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"Thanks for this!" says: | DejaVu (11-09-2015), St George 2013 (11-09-2015) |
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#7 | |||
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Wisest Elder Ever
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I would try and find out.
These drugs are known toxins causing PN today.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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"Thanks for this!" says: |
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#8 | |||
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Senior Member
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Hi Cliffman,
I am sorry you are going through this experience. Some important insights have been offered. Both are worth looking into, for sure. Many doctors still do not admit to the potential damage of use of the antibiotics mentioned by mrsD. I hope you are being followed closely. Is your neurologist aware of the rapid spreading? If not, please let your neurologist know. It's important to get neurology working at finding the cause especially when spreading so quickly. I know from experience, not all neurology departments act quickly; however, please at least be sure your doctors know what's happening, especially if you are in between appointments. Keep reaching out about this. It must be very frightening, frustrating and more. ![]() DejaVu
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May we have the courage to live from our hearts, to allow Love, Faith and Hope to light our paths. . . . |
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"Thanks for this!" says: | St George 2013 (11-09-2015), vintagewine (11-10-2015) |
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#9 | ||
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Member
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Love the video link you included..very uplifting song. Thank you!! Cliffman ![]() |
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"Thanks for this!" says: | St George 2013 (11-19-2015) |
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#10 | ||
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Member
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Hi Cliffman
Just to add another antibiotic to the list to ask about. I was given IV Metrodiazanole during appendectomy a year ago and my PN flared up very badly soon after - still not certain if this was the cause as there were other issues going on but the timing seemed more than coincidental. Good luck with your appt. tomorrow. Hope you get some answers. Let us know how you get on. |
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"Thanks for this!" says: | St George 2013 (11-19-2015) |
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neuropathy spreading rapidly | Chronic Pain | |||
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