Sallysblooms
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Dietary Supplement Labeling Act
Sallysblooms replied to Sallysblooms's topic in Dysautonomia Discussion
Other forums are working hard to keep our supplements available. I have been working on it doing all I can. Calling and emailing is easy, there are no meds that heal. -
Could A Multi Vitamin Help?
Sallysblooms replied to IDreamInColor's topic in Dysautonomia Discussion
My integrative doctor has me take great supplements, the best brands. I take lots of things, but my multi is called Ultra Preventive x by Douglas Labs. Making a smoothie with Greens First, Whey Protein (only a good brand), oatmeal, banana, apple, carrots, froz fruit like blueberries, strawberries or mango, etc. You can get a LOT of antioxidents for your nerves, fiber, nutrition from that. I drink it daily. All of the fruit, veggies, protein, fiber you need. Easy to get what you need like that. Yes, A good magnesium powder is very good. -
Difficulty Sleeping Because Of Sleep Starts
Sallysblooms replied to Rachel's topic in Dysautonomia Discussion
Do you take a good magnesium supplement at night? Also Epsom Salts in your bath is good. Relaxes the muscles amount other things. Safe. -
There is only a month left where we have the opportunity to call our senators/congressmen to tell them if you oppose the Dietary Supplement Labeling Act that threatens to take the freedom people have to buy their supplements. My doctors have helped me with supplements and I do a lot of research to find the best supplements that have helps my POTS, CFS and help my immune system and help me prevent other problems in the future. Supplements have raised my serotonin level so there is no need for the side effects of prescriptions, they are healing the nerves so the autonomic nervous system works better and I am able to do more and more. Other countries cannot buy or import simple vitamins. I hope we never face our loss of freedom to have ways to improve. I think the FDA is over reaching again and I hope we can save them from doing it. In my opinion they do not have reservations about dangerous medicines and side with Pharm. companies that, in my opinion, want to make even more money. For those of you who want to support, it is very fast and easy to call and email. Just google for your senators and congressmen in your state. Calls are important also. Doctors I have talked to are very concerned and patients are also. Links cannot be pasted here I guess, but I hope you will find the places to add your name to a petition. Just like when meds were threatened for some that take them for POTS, it would help if people act.
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My integrative doctor has me on 5HTP twice a day. WONDERFUL for seratonin and sleep. For the other, I can't remember my levels but I take Adrecor from Neuroscience, I used to take Travacor. The line is all about Amino acids and vits that naturally balance them. Does your doctor know about it? A lot of people use the company to test and help levels of n. transmitters.
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Does your doctor understand there are ways to help the nerve damage?
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Newbie, I used to feel awful when I ate meals. Bloated, nausea deluxe.... Just getting better with the POTS has helped. My doctors are working to heal the nerves (supplements) since they control the blood vessels, muscles etc. So my stomach, intestine, heart are all so much better. I used to be SO horribly nauseated every day. I am so thankful that is very rare now. I eat and the food goes down fine now. I am so thankful.
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How Are You Now Compared To 6 Months Ago?
Sallysblooms replied to IDreamInColor's topic in Dysautonomia Discussion
Better each month thankfully! LOTS of supplements, several to heal the neuropathy with POTS for the heart, blood vessels etc.. -
Should Snris Be Avoided By Hyper Pots Patients?
Sallysblooms replied to Annaliese's topic in Dysautonomia Discussion
My POTS started a few months after my hysterectomy. I am not able to take pain killers so it was all quite horrible. I have also had CFS/ME for 20 years so I was primed for it. -
Nothing is a problem now thankfully.
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A New Era Of Medicine Has Finally Arrived
Sallysblooms replied to Dizzysillyak's topic in Dysautonomia Discussion
Deletlng, words were added -
I am very careful of prescriptions and try to not take them. Just for UTI or something where there is no choice since it is an infection. I hate them, so dangerous and many are toxic to the nerves, not what you want with POTS. Supplements are amazing though. They are healing the nerves. I have doctors that know what to tell me to take, amount and brand. No guessing.
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Scared I May Have Vascular Eds (2 Year Waiting List!)
Sallysblooms replied to Lette's topic in Dysautonomia Discussion
Two years, that is unreal.I am so sorry! -
Could A Medication Have Been The Trigger?
Sallysblooms replied to sylvan's topic in Dysautonomia Discussion
Prescription drugs can be very toxic to the nervous system. Very often it is listed right there, "can cause neuropathy.." I only use them if there is no option. Only for UIT's etc. I also make sure I take supplements that heal the nerves. Pres. med is very scary and they have to really be taken seriously. Too many people think they are safe and doctors have no other knowledge and want to give them for every symptom when there are safe ways to heal. -
I Am Burning Up-Can Someone Explain This Please.
Sallysblooms replied to Maiysa's topic in Dysautonomia Discussion
Don't forget about supplements for the autonomic neurpathy. I guess all POTS patients have a nerve problem to some extent since the nerves tell the blood vessels/muscles to contract. They do not work with POTS, so you get pooling and the blood will not stay in the head. Benfotiamine is vit. B1 that is fat and water soluble.That is used for neuropathies. You can google it. Alpha Lipoic Acid is also used to heal neuropathies. Well known. My integrative MD has me taking these as well as a great regemine of supplements. You can research both and if you find an integrative MD, he will know all about them. Odd that many docs do not know. Your doctor will know the best brands and amount to take. I have made great progress with them! -
I have had several. No problems here.
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A New Era Of Medicine Has Finally Arrived
Sallysblooms replied to Dizzysillyak's topic in Dysautonomia Discussion
My integrative MD's have been doing good work for years. I have done great with my CFS and now POTS, no precriptions, I have to stay away from toxic drugs. All supplements, good healthful food. Common sense and great integrative MD's. There are many things to help, most reg. doctors just have no training with supplements. They just write prescriptions... ugg -
I have both also. Love to sit and pedal. The eliptical is so great, works the whole body, but hard to do a lot of it. I used to do more before POTS.
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It is good to know if a doctor can't help. It is best to move on. Find a new doctor, an integrative MD is good. Open minded, more of a scientist.
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Arrogance Must Be A Med School Pre-Req...
Sallysblooms replied to Libby's topic in Dysautonomia Discussion
WOW, so glad he knows all about POTS! -
He should have just faxed it or sent it with you within a day or two.