Posted at April 25, 2014 | By: | Categories: FXCRC and Clinics | 2 Comments

The Fragile X Clinic: What Does It Mean For You?

Importance of Regular Clinic Visits

At our clinic in Boston we often hear families ask why they should go to a Fragile X clinic if they are happy with the care they are currently receiving from their local providers. The main reason is that our clinics specialize in all things Fragile X—we get you and your child. Everyone here—clinicians, genetic counselors, social workers, therapists, and all other members of the clinic—knows fragile X syndrome (FXS).

Specialty Fragile X clinics are a relatively new thing. The Rush University and MIND clinics have been around for a long time, but new clinics are now joining the Fragile X Clinical and Research Consortium (FXCRC). Here are a few reasons why you should visit your local fragile X clinic:

FXCRC Fragile X Clinics

Currently 27 Fragile X Clinics

  • All Fragile X clinics in the FXCRC are connected to each other, providing even the newer clinics with the knowledge and expertise of those who have been in the field for a long period of time.
  • They know about the difficulties families have to face when finding the right services or finding local providers who have heard of Fragile X.
  • Providers in a Fragile X clinic can work with your local providers to help manage any ongoing or acute issues.
  • Although many families are very up-to-date on everything Fragile X-related, the providers at the clinics may know of new information that has not made it to the general public yet.
  • Clinics know what research is being done and in the pipeline, and can help you find research opportunities. The largest project that involves all of the clinics is the FORWARD Registry and Database. You may want to ask about the FORWARD Registry and Database at your next clinic visit.
  • Clinicians at FXCRC clinics go to the NFXF conferences, local conferences, NFXF Advocacy Day, and more! In other words, part of their job is to live Fragile X.

Although all clinics provide medical services and can be your primary care for Fragile X-related issues, the Fragile X clinic does NOT take the place of your primary care provider. Your primary care provider still needs to deal with the everyday things, including illnesses, vaccines, and routine health screenings.

When Should You Visit?

Families ask when or how often they should visit a clinic. I recommend routine yearly or every other year visits. This allows the clinic to get to know you and your family better. We get to know what your child is usually like —when things are going well and when things aren’t going so well. This helps us better assess an acute issue, which can be very difficult when first meeting a patient, or if we have not seen someone for an extended period of time.

Another time to visit the clinic
is when there is a new and
unexpected development.
Another time to visit the clinic is when there is a new and unexpected development. For example, if your child starts to have behavioral problems that were not there before or if they’ve changed schools and you feel the programming isn’t appropriate for them.

Families with a new diagnosis of a Fragile X-associated Disorder (FXD) should also contact their local clinic. Seeing providers with expertise in FXDs can provide the information and support that families need when they receive a new diagnosis.

Many of the Fragile X clinics are based in children’s hospitals and may not be able to see adults.  However, some clinics will not be able to see adults with FXS because it is considered a “pediatric” disorder even though we know its impact is lifelong. It is important to keep in mind that clinics may not be able to refer you to other medical providers within their hospital, but they often have contacts with clinicians who can see adults with FXS. This also applies to individuals with FXTAS or FXPOI, or to those who are suspected to have FXTAS or FXPOI.

For example, in Boston, we have colleagues at other hospitals that we refer to when we get questions about managing or diagnosing FXTAS or FXPOI. Therefore, even if the clinic is in a children’s hospital, it is always worthwhile contacting them to see if they can see adults with FXS or have clinicians they can refer to who know FXS and other FXDs.

What If You Can’t Visit a Clinic Regularly?

We understand that it can be very difficult to travel to a clinic for a variety of reasons. Money can be an issue, as can simply traveling with your child. Clinics can provide letters of medical necessity to help with obtaining insurance approval for a visit.

Justin Silver Fly with Me FundIf financial issues for traveling are an issue, assistance may be available through the Fly With Me Fund.

We understand that traveling with your child can be a challenge. If you have to take a plane, clinics may be able to provide you with a letter to help ease your way through the airport. If you can’t attend a clinic yearly, talk to your providers about checking in by telephone or email on a yearly basis.

While clinic visits can be very stressful for all involved, they are opportunities to show improvements your child has made and to gather information about what is going on in the Fragile X world. Visiting a clinic is also an opportunity to discuss any questions or concerns you may have about your child’s development.

The number of Fragile X clinics continues to grow. If your state doesn’t have a Fragile X clinic, you can talk to your providers about possibly starting a clinic. They in turn can talk to members of the FXCRC about what is involved in starting and maintaining a Fragile X clinic.

Fragile X clinics have a lot to offer by way of evaluations and information, and all of the clinics are invested in FXDs and improving the lives of our patients and families. We look forward to seeing you at one of our clinics!


Sharyn LincolnSharyn Lincoln received her bachelor’s degrees in Biology and Religion at the College of William and Mary, and her MS in Genetic Counseling from Brandeis University. She is currently a licensed genetic counselor practicing at Boston Children’s Hospital, and is the counselor and program coordinator for the Boston Children’s Hospital Fragile X Program. Ms. Lincoln is the co-chair of the Fragile X Clinic and Research Consortium (FXCRC) Executive Council as well as a member of the FXCRC’s Clinical Committee and Research Committee. She is in close communication with the New England Community Support Network groups and actively participates in local Fragile X conferences and events. In addition to her clinical responsibilities, Ms. Lincoln is a member of the Genetics Program quality team, which is responsible for developing and implementing outcome and process measures for the Genetics Program.


  • My three sons are adults. We have visited the Fragile X clinic at Vanderbilt a few years back but it seemed more focused for children rather than adults. I think it’s a great idea for parents to get quickly involved in learning more about their child and how Fragile X is affecting them along with steps already researched can perhaps help their son/daughter get the medication and supports they need. I wish it had been there for my sons but I am thinking for research purposes we may be born before the time.

  • we visited the Hopkins/Kennedy Krieger clinic when our son was almost 2 years old. We got our diagnosis around 6 months earlier and were in the spells of trying to exhaust all the avenues of help or insight. We were enrolled in early intervention at the time and our experience with KK was that it was exactly the evaluations provided by the State, except it cost us >$1000 (after insurance). Basically, they are not geared to handle kids his age, which is understandable as the average age of diagnosis is much later and there are no/very few trials available for those under 5.
    After we moved, I regret not having contacted the local clinic as they are evidently skilled at dealing with local services (and we had and continue to have challenges with the school system to receive such). We do plan to return, however, if only to gauge our son’s progress within the spectrum of FX as well as consider drug trials when he turns 5.

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