Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


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Old 04-16-2014, 11:24 PM #1
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Kemily ,sorry to heard that you are going through such of awful pain,and so stressing situation,is hard for us,mostly we are all adult,I can't imagine how hard is for you live your teen years with this terrible condition,But I'm really amazed of how mature you are,you are able to understand and manage your condition the best you can,you are so brave,if I was one of your parents I definitely will be so proud of you. I had rsd/ crps for more then two years now,let me tell you is been a roller coaster ,highs and downs suddenly everything is different you just try to adapt to the situation,the hard part is get the right pain management dr and your own family support. I think if you feel like trying school go ahead that might distract you but if you definitely feel like going out is bad idea than talk to your parents seriously and make them let you stay at home and get homeschool, like a parent that's my opinion but all is in your hands and stand up for what you feel,show you parents pictures,videos from the internet,you tube, rsds.org is a crps community of America,you can find a lot information there,don't be afraid ,speak up, you need medical treatment ,rsd is real,people think that because they don't see a fracture or a physical injury you are not sick,there are many conditions that you can't see and is doesn't mean you are not sick,if they don't take you to the doctor,call the dr yourself and see things will change,you don't have suffer alone,there is people and places like here,you can learn,talk,listen ,and live less stress because some one care, we all care for each other,especially for someone like you,don't stop the fight,is a long fight but try,keep trying and do research,a lots of research ,rsd can be keep in control,takes time,but you will be able to control the flare ups as long as you take your meds,if you have side effects tell the dr they will try a different combo but tell him/ her what medication is not working so they can adjust your treatment,also physical therapy is essential if you can but if you can get hurt avoid it,hope you get better soon and speak up,don't be afraid or think is wrong ,you are too young to depend of medications to live day by day,you don't need that,changes need to be done,do more research,print then and show then to your family so they can learn to.
Sweet heart,I hope the best,I will pray for you,and blessing to you and your family, we are all here whenever and anytime you need us,your friend Jesika
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Old 04-17-2014, 10:30 AM #2
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Quote:
Originally Posted by kemily18 View Post
Im a 16 year old girl and I have had CRPS since I was 12 due to being hit by a car and my Dad not believing I had 3 fractures in my foot for 6 month without treatment. My CRPS is now all over my body and severe. My doctor is awful and they literally do NOTHING. I take 200 mg Lyrica 3 times a day, 100 mg of Lamictal twice a day, 25 mg benydril at bed time and ibuprofen/Excedrin migraine as needed. I am now home schooled and willing to try anything, home schooling was pressured upon me because my dad thinks I cant handle high school. I am extremely irritable ever since my dose changed to 3 times a day and Im depressed enough as it is. My dad has failed to make another appointment with my former doctor. I just started acupuncture and he told me I should go to an osteopathic doctor and try to get off my medication. Has anyone had any success with holistic approaches? Gotten off all pharmaceuticals? I have to get this under control by August, I HAVE TO GO BACK TO HIGHSCHOOL.
Hi Kemily18,

Like the others have already said, I am so sorry you are dealing with this at such a young age!! Bravo to you for such a strong desire to return to school. Regarding the irritability after the dose of Lyrica changed - this is something I would strongly suggest you get in touch with the physician who ordered that for you. It may be that you need more time for your body to adjust to the new amount but, there are also often timing changes that will allow you the benefits of the meds without feeling the side effects during the daytime hours when you would like to be alert and not irritated. Please contact your doctor and express how it is making you irritable and ask about dosing times to see if there are better options. Also, if you haven't tried Gabapentin or Gralese these work the same way as Lyrica, each person reacts differently to these so it is much of a trial and error in getting the one that works best for you.

Regarding your Dad - have you had a sit down with him to ask him why he isn't scheduling your appointments? I'm guessing he is overwhelmed with CRPS and the effects it has on you and not intentionally preventing you from the care you need. Please sit down with him and express your desire to return to school and the need for proper continuous care. You need him to help you get the tools (meds/treatments/counseling etc.,) you need so that you can get as much of a normal life back. If that doesn't work, I would reach out to a doctor, another family member and ask them to step in and help your dad understand.. like a mediator of sorts.

Personally, I think if your desire is to go to school and you think you can then that is the absolute best treatment you can have at this point. Anything you can do to distract yourself from pain will improve your life. That doesn't mean the pain leaves you but joyful things distract you from it making it more bearable. Don't lose hope on that goal..please. You can do this.. it might not be easy and it might cause hurt feelings but, you can do it.. keep focused on your goal!!

Regarding holistic approaches - I would gladly send you a great book on the many different holistic approaches for pain relief that was written by a doctor at the University of Washing, Seattle. This book is invaluable in my opinion to the daily pain fight we all face. If you send me your email address through a PM I will gift it to you through amazon, that is of course if you would like it.

There are many great treatment options for people your age - have you done much more that what you shared above? The medications you are on are not opiods/narcotics so I would ask why the need to stop them? They are specifically for neuropathic pain and spasticity rather than pain specific medications. Finding out the rationale behind the suggestion may allow for healthy conversation and clarity - please discuss this with all involved in your care.

Try not to worry about new trauma causing CRPS to spread. Sure it is a risk but not everyone has this happen. I have fallen countless times, burned the cwap out of my hand, cut myself etc., and none of those things caused the CRPS to spread to those areas. Living a little more carefully is smart but living in fear everyday of a bump by an unknowing person or heaven forbid you trip is not healthy and will only increase pain/brain connection.

Wishing you the best Kemily18,
Tessa

Last edited by zookester; 04-17-2014 at 12:10 PM. Reason: added "not" intentionally.. oops that was bad typo!
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Old 05-08-2014, 11:17 PM #3
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Quote:
Originally Posted by zookester View Post
Hi Kemily18,

Like the others have already said, I am so sorry you are dealing with this at such a young age!! Bravo to you for such a strong desire to return to school. Regarding the irritability after the dose of Lyrica changed - this is something I would strongly suggest you get in touch with the physician who ordered that for you. It may be that you need more time for your body to adjust to the new amount but, there are also often timing changes that will allow you the benefits of the meds without feeling the side effects during the daytime hours when you would like to be alert and not irritated. Please contact your doctor and express how it is making you irritable and ask about dosing times to see if there are better options. Also, if you haven't tried Gabapentin or Gralese these work the same way as Lyrica, each person reacts differently to these so it is much of a trial and error in getting the one that works best for you.

Regarding your Dad - have you had a sit down with him to ask him why he isn't scheduling your appointments? I'm guessing he is overwhelmed with CRPS and the effects it has on you and not intentionally preventing you from the care you need. Please sit down with him and express your desire to return to school and the need for proper continuous care. You need him to help you get the tools (meds/treatments/counseling etc.,) you need so that you can get as much of a normal life back. If that doesn't work, I would reach out to a doctor, another family member and ask them to step in and help your dad understand.. like a mediator of sorts.

Personally, I think if your desire is to go to school and you think you can then that is the absolute best treatment you can have at this point. Anything you can do to distract yourself from pain will improve your life. That doesn't mean the pain leaves you but joyful things distract you from it making it more bearable. Don't lose hope on that goal..please. You can do this.. it might not be easy and it might cause hurt feelings but, you can do it.. keep focused on your goal!!

Regarding holistic approaches - I would gladly send you a great book on the many different holistic approaches for pain relief that was written by a doctor at the University of Washing, Seattle. This book is invaluable in my opinion to the daily pain fight we all face. If you send me your email address through a PM I will gift it to you through amazon, that is of course if you would like it.

There are many great treatment options for people your age - have you done much more that what you shared above? The medications you are on are not opiods/narcotics so I would ask why the need to stop them? They are specifically for neuropathic pain and spasticity rather than pain specific medications. Finding out the rationale behind the suggestion may allow for healthy conversation and clarity - please discuss this with all involved in your care.

Try not to worry about new trauma causing CRPS to spread. Sure it is a risk but not everyone has this happen. I have fallen countless times, burned the cwap out of my hand, cut myself etc., and none of those things caused the CRPS to spread to those areas. Living a little more carefully is smart but living in fear everyday of a bump by an unknowing person or heaven forbid you trip is not healthy and will only increase pain/brain connection.

Wishing you the best Kemily18,
Tessa
i feel so bad for you...God bless you
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Old 05-09-2014, 01:30 AM #4
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I don't have any sage advice about your father and dealing with that situation. It sounds rough and others have posted lots of advice already. I can say though that if he's pushing for more natural approaches there is one thing I discovered recently that helped some. I thought that the whole essential oils thing was complete quackery and frankly completely stupid. Then I was with my bff the other night and she saw I was in a bad state and called a friend who does the whole oils thing. She came right over and trialed them on me. I know it wasn't a placebo effect because I thought it was dumb. It's worth looking into, even though they can be pricy. As pointed out, the longer I can keep myself (more or less) off serious drugs, the more I'll have available later. Looking into alternatives to hard hitters is a great idea, but keeping away from the daily dose things like lyrica, cymbalta, gabapentin and the like that have the potential to be really helpful just doesn't seem to make sense to me.
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