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BOTOX ® is a therapeutic agent derived from the bacterium, Clostridium Botulinum; Also known as Botulinum Toxin Type A. The brand BOTOX ® is produced in controlled laboratory conditions and given in extremely small therapeutic doses originally for the treatment of blepharospasm (eye spasm) and strabismus (misalignment of the eye). BOTOX ® Purified Neurotoxin Complex is a vacuum-dried form of purified botulinum toxin type A and is being investigated for several conditions associated with overactive muscle activity.
Xeomin ® (incobotulinumtoxinA) is approved by the US FDA for the treatment of adults with blepharospasm. IncobotulinumtoxinA is made from the bacteria that causes botulism. Botulinum toxin blocks nerve activity in the muscles, causing a temporary reduction in muscle activity.
Botulinum products were originally intended for the treatment of blepharospasm (eye spasm). However, BOTOX ® was approved in 2002 for cosmetic applications to improve the look of fine lines and superficial wrinkles caused from every day facial expressions like smiling, frowning or squinting by prohibiting these movements. Doctors can use Xeomin off-label to treat the same facial lines treated by Botox, including frown lines, crow's feet and forehead wrinkles. If you find that the early signs of aging are becoming apparent or if your facial expressions are causing premature wrinkles to appear, then botulinum products may be for you.
They are also used in the prevention or smoothing of wrinkles, by prohibiting you from making the facial gestures that cause wrinkles. They may not remove a static wrinkle completely, they only disallow you from furrowing your brow or squinting a certain part around your eye. If your wrinkles are static then it may lessen them a bit. However, if your wrinkles are superficial it can smooth it considerably so that it appears that they have been removed.
More than 84,000 people worldwide have been treated with Xeomin® injections. The U.S. is actually the 20th country to approve this new drug. The effects of Xeomin ® occur within one week, and the results last from three to six months, making it comparable to Botox in terms of both onset and duration of action.
Normally, your brain sends electrical messages to your muscles so that they can contract and move. The electrical message is transmitted to the muscle by a substance called acetylcholine. Botulinum products work to block the release of acetylcholine and, as a result, the muscle does not receive the message to contract. This means that the muscle spasms or movements that cause wrinkling, stop or are greatly reduced. Patients sometimes refer to the effects of the injection to their area of treatment as being paralyzed.
Risks: There is a risk that all botulinum toxin products may spread from the area where they were injected to other parts of the body, causing potentially life-threatening swallowing and breathing problems. This was predominantly seen in children treated with Botox off-label for cerebral palsy. These issues have not been reported among people who received botulinum products for cosmetic uses or to treat blepharospasm.
Other risks may include bleeding and bruising at the injection site and allergic reactions such as itching, swelling or shortness of breath. Your doctor should discuss all the potential risks of this procedure with you during your consultation.
When Xeomin® is used to treat blepharospasm, the most common side effects of Xeomin were eyelid sagging, dry eye, dry mouth, diarrhea, headache, visual impairment, shortness of breath (dyspnea), and upper respiratory infections.
Warning: Pregnant women must not receive injections of BOTOX ® due to possible crossing of the placenta.
We’re pleased to introduce LATISSE™ (bimatoprost ophthalmic solution) 0.03? – the first and only FDA-approved prescription treatment for hypotrichosis used to grow eyelashes, making them longer, thicker, and darker. Eyelash hypotrichosis is another name for having inadequate or not enough eyelashes.
LATISSE™ has been studied in clinical trials to demonstrate its safety and effectiveness. To see more results or learn more, visit www.latisse.com.
Do not use LATISSE™ solution if you are allergic to one of its ingredients.
LATISSE™ solution is intended for use on the skin of the upper eyelid margins at the base of the eyelashes. DO NOT APPLY to the lower eyelid. If you have a history of abnormal intraocular pressure (IOP), you should only use LATISSE™ under the close supervision of your physician.
LATISSE™ use may cause darkening of the eyelid skin which may be reversible. Although not reported in clinical studies, LATISSE™ use may also cause increased brown pigmentation of the colored part of the eye which is likely to be permanent.
You should tell your physician you are using LATISSE™especially if you have a history of eye pressure problems. You should also tell anyone conducing an eye pressure screening that you are using LATISSE™.
The most common side effects after using LATISSE™ solution are an itching sensation in the eyes and /or eye redness. This was reported in approximately 4% of patients. LATISSE™ solution may cause other less common side effects which typically occur on the skin close to where LATISSE™ is applied, or in the eyes. These include skin darkening, eye irritation, dryness of the eyes, and redness of the eyelids.
Please ask for the full prescribing information.
Come in today for the newest innovation in lashes! To learn more visitwww.latisse.com