Topic: $40 can save your life or your loved one's life...MedicAlert...
Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707
posted
I have once again joined MedicAlert tonight. I am on too many medications now to keep track of, and have conditions when it is very difficult to speak...so...
......
$40 can save your life or your loved one's life...MedicAlert...
Did you know that the fourth leading cause of death in this country is an allergic reaction to medications?
I didn't...
Have you ever been terrified to admit yourself into the ER for fear that you may end up in a worse condition or possibly not make it out?
I have...
Has there ever been a time that you could not explain your Lyme disease diagnosis to the most important people who held your life in their hands?
My time was last week... My friend's time was tonight...
I have joined MedicAlert tonight...and am encouraging each one of you to think this over seriously for yourselves and for your loved ones.
Every year, over 100 million people visit emergency rooms in the United States. Of these, 10 million cannot communicate their needs and medical problems to emergency personnel.
MedicAlert will speak for you if you are unconscious or unable to communicate clearly. Our emergency call center is on duty 365 days a year to ensure your health will be safeguarded in any medical emergency. MedicAlert relays all the pertinent medical information that can impact your treatment in any critical situation. We are on duty 24 hours, every day to make sure your needs are met.
What are the different services that MedicAlert provides?
All new Members are automatically enrolled in the MedicAlert Advantage Service. The benefits of the Advantage Service are outlined below.
Services that are available to Advantage Members: * 24-Hour Emergency Response Service - Supported by on-site Registered Nurses, MedicAlert will relay your vital medical information to emergency personnel. * Family Notification - MedicAlert calls your family contacts and notifies them of your situation, so you won't be alone in an emergency. * Medication Dosage Service - MedicAlert stores your medication dosages, which emergency medical personnel often need. * 24-Hour Customer Service - Make free, unlimited updates to your file, order a new emblem, or ask a question at any time. Someone who cares will always answer the call. * Online Access and Updating - Make instant changes to your personal record, including change of address, adding/discontinuing medications, and new physician information. * Information Storage - Store information such as the brand, model, and deactivation instructions for medical devices and implants. * Advance Directives - You can also store your state-recognized written Advance Directives and Do-Not-Resuscitate orders with MedicAlert for an additional $20.00 per year. * Privacy - All medical and personal information is strictly confidential and is never distributed to unauthorized personnel or organizations.
What kinds of medical conditions are found among members of MedicAlert?
Conditions covered by MedicAlert cover a wide spectrum, from diabetes, to food allergies, to implanted devices. Here is a partial list of the common medical conditions among our Members: * Heart Disease * Diabetes * Epilepsy * Food Allergies * Drug Allergies * Latex Allergies * Autism * Asthma * Alzheimer's Disease * Implanted Medical Device In addition, some of our Members have no known medical conditions, and utilize our services solely as an identification service.
What if I am unable to afford Membership fees?
As a nonprofit, our mission is to protect and save lives. Thanks to the generous donations we receive each year from our members, we are able to offer ``free'' memberships for indigent individuals and nonprofit organizations that are unable to afford the $40 enrollment fee. For more information on sponsored memberships, please contact our Program Development Manager at 800-228-6222 ext. 2412
If you need further assistance or have any questions, please call MedicAlert's Customer Support at 1-888-633-4298. Our Member Services telephone lines are open from 6 a.m. to 7 p.m. Monday through Friday and from 8 a.m. to 5 p.m. on Saturday (Pacific Time). We are closed on Sundays and holidays.
TX Lyme Mom
Frequent Contributor (1K+ posts)
Member # 3162
posted
Melanie, I saw your other topic about your friend with the bad allergic reaction to her medications, so I assume that this is what's prompting you to post this new topic also.
I'm going to suggest, however, if you do decide to register with Medic Alert, that you take a hint from the newly published ILADS treatment guidelines. No wait, maybe that was from our own LLMDs new Patient Handbook instead. Yes, I think it was.
Well, anyway, the suggestion was this. If you must go to another doctor, PCP, ER, whatever, do NOT say you have Lyme disease. Instead, tell them you have "neuroborreliosis" which should be less prejudicial against your chronic, late-stage Lyme diagnosis.
The Steere group has gone to great lengths to publish position statements defining Lyme disease as something which is easily treated with short term antibiotics.
However, they ignore the condition of chronic, persistent "late-stage" Lyme disease altogether. That's where the term "neuroborreliosis" can be used to best advantage.
Therefore, register not only your medication allergies when you buy your Medic Alert bracelet, but be sure to register your underlying health condition as being "neuroborreliosis" -- in order to avoid the necessity for defending your diagnosis of chronic Lyme disease, which isn't going to fly with any of these other doctors.
Afterall, the Steere crowd has covered their bases well by publishing position statements prejudicial against Lyme disease, as defined by them, in the journals read by emergency room physicians, too.
Now is the time to become aware of the advantage of redefining what our illness really is and that is by switching our terminology to the more accurate diagnostic label called "neuroborreliosis".
PS - You might also want to use this "neuroborreliosis" terminology elsewhere, such as when you fill out disability paperwork or whenever you must apply for special accommodations under the federally mandated thing about persons with disabilities, such as for college or public school situations.
[This message has been edited by TX Lyme Mom (edited 29 February 2004).]
I was dx with type 2 diabetes 1-2-04; so I researched and found MEDICAP pharmacy had the best bargain on getting a ID bracelet or necklace for $19.95...printing on both sides.
I put my name, home phone no., & type 2 diabetes on front; back side was everything I was allergic too.
7-12-04 dx w/lyme....neuoborroliosis; so thinking of getting ANOTHER bracelet for lyme & what I'm on. Since new meds are being added monthly/bi-monthly...I'm waiting for now.
At least I'm wearing one w/allergic info! Betty G., Iowa
I also hadn't heard of jointing medic alert; so thank you!
Posts: 1 | From US | Registered: Aug 2015
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Kara Tyson
Frequent Contributor (5K+ posts)
Member # 939
posted
It is very important. I was taken to the ER once being barely able to communicate. I said I had Lyme...they could not understand me and wrote down that I was BLIND.
Posts: 6022 | From Mobile, AL | Registered: Apr 2001
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posted
I have two medic alert charms, one gold, one silver. I had lobster claws put on them and I have retrofitted my existing jewelry to incorporate the medic alert charms.
My meds switch a lot, and lots of meds are contraindicated or cannot be prescribed, so I also carry an updated meds list with me at all times, and my friends know how to access the list.
posted
I got Dominic a medic alert neck-a-lace to show lyme disease and heparin.
He picked it out, of couse he got the cool one and it was 60.00 but worth it, also in that cost was to have his name engraved on the front of it.
Alot of places I spoke to refused to do this because if a stanger comes up to the child they will see his name ect..
I figured if he lost it, possibly someone would recognize his name (school, church, places we go to frequently) and we have a better chance of getting it back.
This is a great idea and it makes me not worry so much if he is in a car wreck or hurt they could see he was on heparin.
Problem: he just got off heparin but the place said they could either "fill it" or scratch threw it. I am waiting until we know for sure he is off for good.
posted
I bought mine locally at our MEDICAP pharmacy 5 yrs. ago in jan. at that time it was less than $20.
i used BOTH side for info!! name, phone no. & diabetes 2 on front
back: all allergies !! penicillin, multi chemical sensitivities,
i talked to EMT's later asking about putting LYME DISEASE on there; NOPE; it means nothing to us.
melanie's post above is great and lists all the IMPORTANT HEALTH ISSUES to be placed on yoru id bracelet or necklace!!
i've got the bracelet & lose; too tight otherwise.
thanks melanie for bringing this up again since there are so many other issues caused by lyme:
heart block, kidneys, blood issues, etc.
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bettyg
Unregistered
posted
I bought mine locally at our MEDICAP pharmacy 5 yrs. ago in jan. at that time it was less than $20.
i used BOTH side for info!! name, phone no. & diabetes 2 on front
back: all allergies !! penicillin, multi chemical sensitivities,
i talked to EMT's later asking about putting LYME DISEASE on there; NOPE; it means nothing to us.
melanie's post above is great and lists all the IMPORTANT HEALTH ISSUES to be placed on yoru id bracelet or necklace!!
i've got the bracelet & lose; too tight otherwise.
thanks melanie for bringing this up again since there are so many other issues caused by lyme:
heart block, kidneys, blood issues, etc.
IP: Logged |
Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707
posted
You are most welcome Miss B.
Posts: 7052 | From Colorado | Registered: Mar 2003
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
-
While Medic Alert tag can be informative, if lyme is on one's medic alert tag, some doctors would just as soon leave the patient at the door step - even if they are there for other reasons.
That has happened twice to me - not there for lyme, but they saw that in my history and refused treatment, sending me away (after paramedics nearly forced me to go).
I actually heard the two ER doctors discuss this once outside the room, before they even saw me. "We're not going to do anything for her," the main doc told the intern. "Nothing?, he said?" Nope. We don't treat lyme here.
But I had been there for other reasons.
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[ 04-30-2009, 12:16 PM: Message edited by: Keebler ]
Posts: 48021 | From Tree House | Registered: Jul 2007
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Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707
posted
I understand your hesitancy Keebler...but you can call them and have ANYTHING written on your bracelet.
Actually, there is not much room for writing on the bracelet itself except for your ID number, that is why they call the emergency number to get your info when the bracelet, necklace, tag, whatever is seen by emergency personnel.
I have listed:
Lyme disease (you can ask to have Neuroborelliosis)
Bartonella
Babesiosis
Ehrliciosis (one day I will learn how to spell this)
and Asthma
Then, they KNOW I have multiple conditions that I am dealing with and multiple medications.
You can also give up to 5 contact numbers.
I also made sure they listed that corticosteroids are strictly contra-indicated except in cases of extreme emergency.
Posts: 7052 | From Colorado | Registered: Mar 2003
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
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I know. I had one until last year. With porphryia, it is important as the wrong drug could just do me in.
I just am too tired to renew it, but your reminder comes probably just in time to keep my old number.
Wow, in California, the ER doctors know about tick-borne infections? That would be such a different world from the state just to your north. I can't even imagine a doctor here taking any of those on your bracelet seriously. But I'm glad they do for you.
Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707
posted
I am so sorry that you have such a difficult time getting healthcare professionals to do their job! It is just so wrong!
And actually, there are MANY ER docs that I have had to educate on TBDs (even in CA). However, IF I am unable to speak, they will at least know what meds I am on and who to contact to speak for me. Including my health advocate and physician.
Posts: 7052 | From Colorado | Registered: Mar 2003
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Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707
posted
And BTW...I met a lovely LL physician in training from Oregon at one of my last apts! So, there is some hope!
Posts: 7052 | From Colorado | Registered: Mar 2003
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
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Melanie,
I actually came back to delete my negative sounding posts but it would through this all out of sequence with your replies reference my tales of woe.
Hey, that is good news about the LL physician in training from this state. I wonder if they will let him/her come back home to work? Hope so.
Travel can be so enlightening for doctors.
Any your having met them will surely have helped them learn more about this.
I'm afraid that my having met the ER doctors here, I made a very bad impression, for when the intercom over my head shouted out for something, my body flew into a seizure and the ER docs accused me of trying to throw myself off the table and the told me to get out.
Another time, a similar thing happened in the waiting room when a phone rang. As I was trying to regain my abilities, spazing out on the floor, the ER nurse kicked my leg and said "I saw you throw yourself off that chair, now get up, NOW!"
But, maybe for the next lyme patient they encounter, they will understand if they see the same reaction to sudden noise.
Thanks for all your efforts at education. You are making such a difference. And, hey, If you see that doctor again, find out where they will be going next, eh?)
Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707
posted
My Dearest,
Please do not ever feel badly for speaking your truth...I am certain you are not the only patient who has had to endure such inhumane treatment. My heart SO goes out to you...
Yes, the new physician was already practicing in OR, and was simply here for a few days to shadow my doc to learn more about TBD patients as she was already trying to treat a few.
I would be happy to get her contact info for you at my next apt toward the end of May, if you would so desire. PLEASE remind me though...I tend to forget easily these days.
I know of so many who experience seizure activity and it is never a pretty sight... but it is frightening for the patient and the ones who witness it...IF they have compassion. I am SO sorry for your suffering, NO ONE deserves to go through what you have.
Much love to you, M
Posts: 7052 | From Colorado | Registered: Mar 2003
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